[go: up one dir, main page]

US20100179441A1 - Device control device and device control method - Google Patents

Device control device and device control method Download PDF

Info

Publication number
US20100179441A1
US20100179441A1 US12/663,342 US66334208A US2010179441A1 US 20100179441 A1 US20100179441 A1 US 20100179441A1 US 66334208 A US66334208 A US 66334208A US 2010179441 A1 US2010179441 A1 US 2010179441A1
Authority
US
United States
Prior art keywords
change
change amount
parameter
unit
user
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US12/663,342
Other languages
English (en)
Inventor
Etsuko Kanai
Masami Funakura
Yasutaka Maeda
Makiko Noda
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Panasonic Corp
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Assigned to PANASONIC CORPORATION reassignment PANASONIC CORPORATION ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: NODA, MAKIKO, MAEDA, YASUTAKA, FUNAKURA, MASAMI, KANAI, ETSUKO
Publication of US20100179441A1 publication Critical patent/US20100179441A1/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/16Devices for psychotechnics; Testing reaction times ; Devices for evaluating the psychological state
    • A61B5/18Devices for psychotechnics; Testing reaction times ; Devices for evaluating the psychological state for vehicle drivers or machine operators
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/02Detecting, measuring or recording for evaluating the cardiovascular system, e.g. pulse, heart rate, blood pressure or blood flow
    • A61B5/021Measuring pressure in heart or blood vessels
    • A61B5/02108Measuring pressure in heart or blood vessels from analysis of pulse wave characteristics
    • A61B5/02116Measuring pressure in heart or blood vessels from analysis of pulse wave characteristics of pulse wave amplitude
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/72Signal processing specially adapted for physiological signals or for diagnostic purposes
    • A61B5/7235Details of waveform analysis
    • A61B5/7239Details of waveform analysis using differentiation including higher order derivatives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B2560/00Constructional details of operational features of apparatus; Accessories for medical measuring apparatus
    • A61B2560/02Operational features
    • A61B2560/0242Operational features adapted to measure environmental factors, e.g. temperature, pollution
    • A61B2560/0247Operational features adapted to measure environmental factors, e.g. temperature, pollution for compensation or correction of the measured physiological value
    • A61B2560/0252Operational features adapted to measure environmental factors, e.g. temperature, pollution for compensation or correction of the measured physiological value using ambient temperature
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/02Detecting, measuring or recording for evaluating the cardiovascular system, e.g. pulse, heart rate, blood pressure or blood flow
    • A61B5/024Measuring pulse rate or heart rate
    • A61B5/0245Measuring pulse rate or heart rate by using sensing means generating electric signals, i.e. ECG signals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/72Signal processing specially adapted for physiological signals or for diagnostic purposes
    • A61B5/7203Signal processing specially adapted for physiological signals or for diagnostic purposes for noise prevention, reduction or removal
    • A61B5/7207Signal processing specially adapted for physiological signals or for diagnostic purposes for noise prevention, reduction or removal of noise induced by motion artifacts
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/72Signal processing specially adapted for physiological signals or for diagnostic purposes
    • A61B5/7271Specific aspects of physiological measurement analysis
    • A61B5/7296Specific aspects of physiological measurement analysis for compensation of signal variation due to stress unintentionally induced in the patient, e.g. due to the stress of the medical environment or examination

Definitions

  • the present invention relates to device control devices for controlling on-vehicle devices, and in particular to a device control device for evaluating the health condition of a person based on a change in a vital sign, and performing device control suitable for the evaluated health condition in order to make better the person's health condition.
  • One technique proposed in view of these problems as a method for discriminating a specific health condition of a person in the case where the person has a stress from a specific health condition of a person in the case where the person is doing sports is a technique for measuring a pulse wave, calculating pulse wave values, the upper peak values of the pulse wave, and the pulse pressure values each of which is the difference between an upper peak value and a corresponding lower peak value of the pulse wave, and determining a current status from among stress, sleepiness, fatigue (muscle fatigue) (See Patent Reference 1, for example).
  • FIG. 1 is a block diagram showing the structure of a health condition discrimination device disclosed in Patent Reference 1.
  • the health condition discrimination device includes a pulse wave measurement unit 1301 , a calculation unit 1302 , a discrimination unit 1303 , and an alert output unit 1304 .
  • the pulse wave measurement unit 1301 measures the flow amount of haemoglobin carried by oxygen and the flow amount of haemoglobin not carried by oxygen which are generated through blood circulation.
  • the calculation unit 1302 calculates data of pulse values, blood pressure values, and pulse pressure values each of which is the difference between the upper and lower peaks of a corresponding one of the pulse waves, based on the pulse wave data measured by the pulse wave measurement unit 1301 .
  • the discrimination unit 1303 detects changes in the data calculated by the calculation unit 1302 , and discriminates the health conditions into plural levels.
  • the alert output unit 1304 outputs alerts according to the levels discriminated by the discrimination unit 1303 .
  • VPG velocity plethysmogram
  • Patent Reference 1 Japanese Unexamined Patent Application Publication No. 2003-61921 (page 8, FIG. 2)
  • Patent Reference 2 Japanese Patent Publication No. 3835073
  • the health condition discrimination device structured according to Patent Reference 1 determines the health condition of a user using a pulse wave.
  • the health condition discrimination device can determine the health condition such as fatigue, stress or sleepiness, it is not sure whether or not the change in the pulse wave is made due to the influence of the determined health condition considering that a pulse wave is a vital sign also susceptible to a thermal environment. Accordingly, the health condition is determined based on the pulse wave affected by the thermal environment, which causes a problem that an erroneous result is highly likely to be outputted.
  • a pulse wave is significantly susceptible to body movements, in addition to health conditions, and thermal sensations.
  • FIG. 2 shows a pulse waveform affected by body movements. The pulse waveform is affected by body movements in Segments A and B, while the pulse waveform is not affected by body movements in the other segments. In this way, the pulse waveform is found to be changed significantly due to the influence of the body movements.
  • FIG. 3 shows a pulse waveform affected by changes in thermal sensation. The pulse waveform is affected by changes in the thermal sensation in Segment C, while the pulse waveform is not affected by changes in the thermal sensation in the other segments. In this way, the pulse waveform is found to be changed significantly due to the influence of the thermal sensations.
  • FIG. 4 shows a solid-line graph representing the variance values of the peak values of velocity plethysmogram ( FIG. 5 ) obtained by performing first-order derivative on the pulse waveform shown in FIG. 2 , and shows a broken-line graph representing the variance values of the peak values of velocity plethysmogram ( FIG. 6 ) obtained by performing first-order derivative on the pulse waveform shown in FIG. 3 .
  • the variance in Segment C affected by a thermal sensation may be smaller than the variance in Segment A affected by body movements, and may be greater than the variance in Segment B affected by body movements.
  • the conventional method according to Patent Reference 1 entails a problem that it is impossible to determine whether a pulse wave change indicates either a pulse wave sign made due to a change in thermal sensation or noise caused due to the influence of body movements.
  • the present invention has been made to solve the aforementioned problems.
  • the present invention has an object to provide a device control device intended to evaluate a user's health condition based on a vital sign such as a pulse wave and perform device control, more specifically, to firstly determine whether or not a change in the vital sign is made due to the influence of a thermal environment so as to discriminate between the influence of a thermal environment and the influence of a health condition, and to perform device control for reliably making better the user's health condition.
  • a device control device is for controlling an on-vehicle device based on a vital sign of a user
  • the device control device includes: a vital sign measurement unit configured to measure, in time series, the vital sign of the user; a parameter extraction unit configured to extract time-series parameter values for evaluating current statuses of the user based on the vital sign measured continuously by the vital sign measurement unit; a determination unit configured to determine whether a factor of a change in the vital sign is a change in a health condition of the user or a change in an environment temperature around the user, based on the parameter values extracted by the parameter extraction unit; and a control unit configured to control the on-vehicle device based on a result of the determination made by the determination unit.
  • the use of parameter values extracted from a vital sign makes it possible to determine a factor of a change in the vital sign, that is, either a change in the user's health condition or a change in the environment temperature around the user. For this, it is possible to control an on-vehicle device based on the determination result. Accordingly, it is possible to evaluate a user's health condition based on a vital sign such as a pulse wave and perform device control, more specifically, to discriminate between a vital sign change due to the influence of a thermal sensation and a vital sign change due to the influence of the health condition, and to perform device control for reliably making better the user's health condition.
  • a vital sign such as a pulse wave
  • the determination unit includes: a parameter change amount calculation unit configured to calculate, for each of the parameter values extracted by the parameter extraction unit, a change amount from a starting point which is the change amount between the parameter value extracted by the parameter extraction unit at a predetermined starting time point and a current parameter value; a parameter change time calculation unit configured to calculate, for each of the parameter values extracted by the parameter extraction unit, change time from the starting time point to a current time point at which the current parameter value is extracted; and a change factor determination unit configured to: make a first determination that the factor of the change in the vital sign is the change in the health condition of the user when (i) the change amount from the starting point calculated by the parameter change amount calculation unit is greater than a threshold value for the change amount from the starting point and (ii) the time required for the change calculated by the parameter change time calculation unit is greater than a threshold value for the time required for the change; and make a second determination that the factor of the change in the vital sign is the change in the environment temperature around the user when (i) the change amount
  • control unit includes: a thermal sensation evaluation unit configured to evaluate a thermal sensation level of the user based on the change amount from the starting point of the parameter value calculated by the parameter change amount calculation unit when the change factor determination unit determines that the factor of the change in the vital sign is the change in the environment temperature around the user; and a control unit configured to control the on-vehicle device based on the result of the evaluation made by the thermal sensation evaluation unit.
  • control unit further includes a health condition evaluation unit configured to evaluate a current health condition of the user based on the change amount from the starting point of the parameter value calculated by the parameter change amount calculation unit when the change factor determination unit determines that the factor of the change in the vital sign is the change in the health condition of the user, and the control unit is further configured to control the on-vehicle device based on the result of the evaluation made by the health condition evaluation unit.
  • a health condition evaluation unit configured to evaluate a current health condition of the user based on the change amount from the starting point of the parameter value calculated by the parameter change amount calculation unit when the change factor determination unit determines that the factor of the change in the vital sign is the change in the health condition of the user
  • the determination unit includes: a parameter change amount calculation unit configured to calculate, for each of the parameter values extracted by the parameter extraction unit, a change amount from a starting point which is a change amount between a parameter value extracted by the parameter extraction unit at a predetermined starting time point and a current parameter value; an environment temperature measurement unit configured to measure, in time series, a current environment temperature around the user; a unit for calculating a temperature change amount from a starting point which calculates, for each of the environment temperatures measured by the environment temperature measurement unit, a temperature change amount from a starting point which is a change amount between an environment temperature at the starting point measured by the environment temperature measurement unit and a current environment temperature; and a change factor determination unit configured to: determine that the factor of the change in the vital sign is the change in the health condition of the user when (i) the change amount from the starting point calculated by the parameter change amount calculation unit is greater than a predetermined threshold value for the change amount from the starting point and (ii) the temperature change amount from the starting point calculated by the temperature change
  • the factor of the vital sign change considering the change amount of the vital sign and the change amount of the environment temperature at the time of the change in the user's vital sign, and control the on-vehicle device based on the determined factor. Accordingly, it is possible to evaluate a user's health condition based on a vital sign such as a pulse wave and perform device control, more specifically, to discriminate between a vital sign change due to the influence of a thermal environment and a vital sign change due to the influence of the health condition, and to perform device control for reliably making better the user's health condition.
  • a vital sign such as a pulse wave
  • the determination unit includes: a parameter change amount calculation unit configured to calculate, for each of the parameter values extracted by the parameter extraction unit, a change amount from a starting point which is a change amount between a parameter value extracted by the parameter extraction unit at a predetermined starting time point and a current parameter value; a parameter change amount integration unit configured to calculate, for each of the parameter values extracted by the parameter extraction unit, an integration value of change amounts each from a previous point, the integration value being obtained by integrating the parameter values extracted by the parameter extraction unit in a period from the starting time point to a time point at which the current parameter value is extracted; and a change factor determination unit configured to: determine that the factor of the change in the vital sign is the change in the health condition of the user when (i) the change amount from the starting point calculated by the parameter change amount calculation unit is greater than a predetermined threshold value for the change amount from the starting point and (ii) the integration value of the parameter values up to the current parameter value extracted by the parameter extraction unit is greater than a predetermined threshold value for the
  • the device control device further includes a vehicle information obtainment unit configured to obtain information about a status of a vehicle driven by the user
  • the determination unit includes: a parameter change amount calculation unit configured to calculate, for each of the parameter values extracted by the parameter extraction unit, a change amount from a starting point which is a change amount between a parameter value extracted by the parameter extraction unit at a predetermined starting time point and a current parameter value; and a determination unit configured to determine whether the factor of the change in the vital sign is the change in the health condition of the user or the change in the environment temperature around the user, based on the change amount from the starting point calculated by the parameter change amount calculation unit and the vehicle status obtained by the vehicle information obtainment unit.
  • the factor of the vital sign change considering the change amount of the vital sign and the status of the vehicle at the time of the change in the user's vital sign, and control the on-vehicle device based on the determined factor. Accordingly, it is possible to evaluate a user's health condition based on a vital sign such as a pulse wave and perform device control, more specifically, to discriminate between a vital sign change due to the influence of a thermal environment and a vital sign change due to the influence of the health condition, and to perform device control for reliably making better the user's health condition.
  • a vital sign such as a pulse wave
  • the vehicle information obtainment unit is configured to obtain a ratio of time during which an acceleration calculated from a handle operation amount at the time when the user operates a handle of the vehicle exceeds a predetermined threshold value during a period from the predetermined starting time point to a current time point
  • the change factor determination unit is configured to: determine that the factor of the change in the vital sign is the change in the health condition of the user when (i) the change amount from the starting point calculated by the parameter change amount calculation unit is greater than the predetermined threshold value for the change amount from the starting point and (ii) the ratio calculated by the vehicle information obtainment unit is greater than the predetermined threshold value
  • the factor of the change in the vital sign is the change in the environment temperature around the user when (i) the change amount from the starting point calculated by the parameter change amount calculation unit is greater than the predetermined threshold value for the change amount from the starting point and (ii) the ratio calculated by the vehicle information obtainment unit is not greater than the predetermined threshold value.
  • the ratio is regarded as the ratio of the time while the steering wheel is being operated. In the case where the ratio of the time while the steering wheel is being operated is great, it is determined that the user's vital sign is changing due to the influence of the user's health condition.
  • the device control device further includes a vehicle information obtainment unit configured to obtain information about a status of a vehicle driven by a user
  • the determination unit includes: a parameter change amount calculation unit configured to calculate, for each of the parameter values extracted by the parameter extraction unit, a change amount from a starting point which is a change amount between a parameter value extracted by the parameter extraction unit at a predetermined starting time point and a current parameter value; a parameter change time calculation unit configured to calculate, for each of the parameter values extracted by the parameter extraction unit, time required for a change which is time from the starting time point to a time point at which the current parameter value is extracted; and a change factor determination unit configured to determine whether the factor of the change in the vital sign is the change in the health condition of the user or the change in the environment temperature around the user, based on the change amount from the starting point calculated by the parameter change amount calculation unit, the time required for the change calculated by the parameter change time calculating unit, and the vehicle status obtained by the vehicle information obtainment unit.
  • the factor of the vital sign change considering the change amount of the vital sign, the time required for the change, and the status of the vehicle at the time of the change in the user's vital sign, and control the on-vehicle device based on the determined factor. Accordingly, it is possible to evaluate a user's health condition based on a vital sign such as a pulse wave and perform device control, more specifically, to discriminate between a vital sign change due to the influence of a thermal environment and a vital sign change due to the influence of the health condition, and to perform device control for reliably making better the user's health condition.
  • a vital sign such as a pulse wave
  • the vital sign measurement unit is configured to measure, in time series, pulse wave data indicating a pulse wave of the user
  • the parameter extraction unit is configured to extract time-series parameter values for evaluating the pulse wave, from the time-series pulse wave data measured by the vital sign measurement unit.
  • the parameter extraction unit extract, in time series, one of (i) an amplitude of a pulse waveform, (ii) either waveform components or waveform component ratios in an accelerated plethysmogram obtainable by performing second-order derivative on the pulse waveform, (iii) parameters obtainable by performing frequency analysis on each pulse wave interval, and (iv) Maximum Lyapunov exponents obtainable by performing chaotic analysis on the pulse wave data.
  • control unit includes: a health condition evaluation unit configured to evaluate the health condition of the user based on the parameter values when the determination unit determines that the factor of the change in the vital sign is the change in the health condition of the user; a thermal sensation evaluation unit configured to evaluate a thermal sensation level of the user based on the parameter values when the determination unit determines that the factor of the change in the vital sign is the change in the environment temperature around the user; and a control unit configured to control the on-vehicle device based on the result of the evaluation made by either the health condition evaluation unit or the thermal sensation evaluation unit.
  • the present invention can be implemented not only as a device control device including various unique processing units as described above, but also as a device control method including the steps corresponding to the unique processing units included in the device control device, and also as a program causing a computer to execute the unique steps included in the device control method.
  • a program can be distributed using recording media such as CD-ROMs (Compact Disc-Read Only Memory) and can also be distributed via communication networks such as the Internet.
  • the present invention provides a device control device that evaluates a user's health condition based on a vital sign such as a pulse wave and controls a device, more specifically, the device control device discriminates the influence of a thermal environment and the influence of a health condition by firstly determining whether or not a change in the vital sign is made due to the influence of the thermal environment, and performs reliable device control for making better the user's health condition.
  • a vital sign such as a pulse wave
  • the device control device discriminates the influence of a thermal environment and the influence of a health condition by firstly determining whether or not a change in the vital sign is made due to the influence of the thermal environment, and performs reliable device control for making better the user's health condition.
  • FIG. 1 is a block diagram showing the structure of a conventional health condition discrimination device.
  • FIG. 2 is a diagram showing a pulse waveform affected by body movements.
  • FIG. 3 is a diagram showing a pulse waveform affected by changes in the thermal sensation.
  • FIG. 4 is a diagram showing (i) a graph representing variance of the peak values of velocity plethysmogram obtained by performing first-order derivative on the pulse waveform shown in FIG. 2 , and (ii) a graph representing the variance of the peak values of velocity plethysmogram obtained by performing first-order derivative on the pulse waveform shown in FIG. 3 .
  • FIG. 5 is a diagram showing a velocity plethysmogram affected by body movements.
  • FIG. 6 is a diagram showing a velocity plethysmogram affected by changes in the thermal sensation.
  • FIG. 7 is a block diagram showing the structure of a device control device according to Embodiment 1 of the present invention.
  • FIG. 8 is a block diagram showing the detailed structure of a vital sign measurement unit.
  • FIG. 9 is a graph showing the ratio of each of maximum values and the corresponding one of minimum values (the ratio is obtained by dividing the minimum value by the maximum value) of the velocity plethysmogram extracted, on a per predetermined time range basis, based on (i) the velocity plethysmogram data affected by the body movements shown in FIG. 5 and (ii) the velocity plethysmogram data affected by the changes in the thermal sensation shown in FIG. 6 .
  • FIG. 10 is a graph showing the variance in the ratio of each of maximum values and a corresponding one of minimum value (the minimum value/the maximum value) of the velocity plethysmogram extracted, on a per predetermined time range basis, based on (i) the velocity plethysmogram data affected by the body movements shown in FIG. 5 and (ii) the velocity plethysmogram data affected by the changes in the thermal sensation shown in FIG. 6 .
  • FIG. 11 is a flowchart of processing performed by the device control device according to Embodiment 1 of the present invention.
  • FIG. 12 is a flowchart of processing performed by the change factor determination unit according to Embodiment 1 of the present invention.
  • FIG. 13 is a diagram showing a data table used for determining the factor of a change in the pulse wave amplitude stored by the change factor determination unit according to Embodiment 1 of the present invention.
  • FIG. 14 shows graphs showing changes in the thermal sensation and fatigue level in the case where the environment temperature changes.
  • FIG. 15 is a diagram showing reaction time for thermal sensations and reaction time for fatigue levels.
  • FIG. 16 is a diagram for illustrating a threshold value for starting point change time used for discriminating between thermal sensations and fatigue levels.
  • FIG. 17 is a flowchart of processing performed by the vital sign measurement unit.
  • FIG. 18 is a diagram of a waveform representing temporal changes in a velocity plethysmogram.
  • FIG. 19 is a diagram for illustrating the starting position of a noise segment.
  • FIG. 20 is a diagram for illustrating the ending position of the noise segment.
  • FIG. 21 is a diagram for illustrating removal of noise from pulse wave data.
  • FIG. 21( a ) is a graph representing temporal changes in the amplitude value of Wave a that is a first wave of the velocity plethysmogram which has not yet been subjected to the noise removal.
  • FIG. 21( b ) is a graph representing temporal changes in the amplitude value of Wave a of the velocity plethysmogram which has been subjected to the noise removal.
  • FIG. 22 is a diagram showing an exemplary waveform of the velocity plethysmogram.
  • FIG. 23 is a block diagram showing the structure of a device control device according to Embodiment 2 of the present invention.
  • FIG. 24 is a flowchart of processing performed by the device control device according to Embodiment 2 of the present invention.
  • FIG. 25 is a flowchart of processing performed by a change factor determination unit according to Embodiment 2 of the present invention.
  • FIG. 26 is a diagram showing a data table used for determining the factor of a change in the pulse wave amplitude stored by the change factor determination unit according to Embodiment 2 of the present invention.
  • FIG. 27 is a diagram for illustrating a threshold vale for the temperature change amount from a starting point for discriminating between thermal sensations and fatigue levels.
  • FIG. 28 is a block diagram showing the structure of a device control device according to Embodiment 3 of the present invention.
  • FIG. 29 is a flowchart of processing performed by the device control device according to Embodiment 3 of the present invention.
  • FIG. 30 is a flowchart of processing performed by the change factor determination unit according to Embodiment 3 of the present invention.
  • FIG. 31 is a diagram showing a data table used for determining the factor of a change in the pulse wave amplitude stored by the change factor determination unit according to Embodiment 3 of the present invention.
  • FIG. 32 is a block diagram showing the structure of a device control device according to Embodiment 4 of the present invention.
  • FIG. 33 is a block diagram showing the detailed structure of a vital sign measurement unit according to Embodiment 4 of the present invention.
  • FIG. 34 is a flowchart of processing performed by the device control device according to Embodiment 4 of the present invention.
  • FIG. 35 is a flowchart of processing performed by the change factor determination unit according to Embodiment 4 of the present invention.
  • FIG. 36 is a diagram showing a data table used for determining the factor of a change in the pulse wave amplitude stored by the change factor determination unit according to Embodiment 4 of the present invention.
  • FIG. 37 is a diagram for illustrating a threshold vale for handle operation data used for discriminating between thermal sensations and fatigue levels.
  • FIG. 38 is a flowchart of processing performed by a thermal sensation related device control unit according to Embodiment 4 of the present invention.
  • FIG. 39 is a flowchart of processing performed by a fatigue related device control unit according to Embodiment 4 of the present invention.
  • FIG. 40 is a block diagram showing the structure of a device control device according to Embodiment 5 of the present invention.
  • FIG. 41 is a flowchart of processing performed by the device control device according to Embodiment 5 of the present invention.
  • FIG. 42 is a flowchart of processing performed by the change factor determination unit according to Embodiment 5 of the present invention.
  • FIG. 43 is a block diagram showing the structure of a vital sign measurement unit.
  • FIG. 44 is a flowchart of processing performed by the vital sign measurement unit according to Embodiment 5 of the present invention.
  • FIG. 7 is a block diagram showing the structure of a device control device according to Embodiment 1 of the present invention.
  • the device control device shown in FIG. 7 is configured with known computers for example, and includes a vital sign measurement unit 101 , a parameter extraction unit 102 , a determination unit 120 , and a control unit 130 . These processing units function when the program is executed by a CPU of a computer storing an installed device control program designed according to this embodiment.
  • the vital sign measurement unit 101 samples a user's finger-tip pulse wave detected by a known transducer or the like at a predetermined sampling cycle, and obtains pulse wave data in time series.
  • the parameter extraction unit 102 extracts the amplitude of the pulse waveform from the pulse wave data as parameter values for evaluating the pulse wave, and accumulates the parameter values.
  • the determination unit 120 is a processing unit for determining the factor of a change in the pulse wave data using the parameter values extracted by the parameter extraction unit 102 .
  • the determination unit 120 includes a parameter change amount calculation unit 103 , a parameter change time calculation unit 104 , and a change factor determination unit 105 .
  • the parameter change amount calculation unit 103 calculates, as a change amount from a starting point, the difference between the value at the predetermined starting time point and the value at a current time point in the time-series data of the pulse wave amplitude extracted by the parameter extraction unit 102 , (ii) calculates, as a previous change amount, the difference between the value at the previous measurement time point and the value at the current time point, and (iii) outputs the change amount from the starting point and the previous change amount to the change factor determination unit 105 .
  • the parameter change time calculation unit 104 calculates, as change time from the starting point, an elapsed time from the predetermined starting time point to the current time point in the pulse wave amplitude extracted by the parameter extraction unit 102 , and outputs the change time from the starting point to the change factor determination unit 105 .
  • the change factor determination unit 105 determines the factor of the change in the pulse wave amplitude (the factor is, for example, the influence of a thermal sensation or the influence of a health condition), based on (i) the change amount from the starting point and the previous change amount calculated by the parameter change amount calculation unit 103 and (ii) the change time from the starting point calculated by the parameter change time calculation unit 104 . Based on the determined factor, the change factor determination unit 105 selects the best evaluation unit from among a thermal sensation evaluation unit 108 and a health condition evaluation unit 109 included in a later-described status evaluation unit 106 , and outputs, to the selected evaluation unit, the current change amount from the starting point that is information to be used for evaluating the current status.
  • the factor is, for example, the influence of a thermal sensation or the influence of a health condition
  • the control unit 130 is a processing unit for performing device control based on the result of the determination made by the change factor determination unit 105 , and includes the status evaluation unit 106 and a device control unit 107 .
  • the status evaluation unit 106 includes (i) the thermal sensation evaluation unit 108 for evaluating a user's thermal sensation based on the change amount from the starting point in the pulse wave amplitude and (ii) the health condition evaluation unit 109 for evaluating a user's health condition based on the same change amount from the starting point in the pulse wave amplitude.
  • the thermal sensation evaluation unit 108 evaluates the user's thermal sensation based on the change amount from the starting point outputted by the change factor determination unit 105 , and outputs the evaluation result to the device control unit 107 .
  • the health condition evaluation unit 109 evaluates the user's health condition based on the change amount from the starting point outputted by the change factor determination unit 105 , and outputs the evaluation result to the device control unit 107 .
  • Thermal sensations include not only a thermal sensation but also an omen of a change in a vital sign before the perception of the thermal sensation.
  • the change factor determination unit 105 outputs the current change amount from the starting point as the information to be used for evaluating the thermal sensation, and the thermal sensation evaluation unit 108 evaluates the user's thermal sensation based on the change amount from the starting point.
  • the change factor determination unit 105 outputs the previous change amount as the information to be used for evaluating the thermal sensation, and the thermal sensation evaluation unit 108 evaluates the user's thermal sensation based on the previous change amount.
  • the device control unit 107 Based on either the thermal sensation evaluated by the thermal sensation evaluation unit 108 or the health condition evaluated by the health condition evaluation unit 109 , the device control unit 107 performs either (i) device control for notifying the user of the evaluation result of the user's thermal sensation or the user's health condition, or (ii) device control for making better the user's thermal sensation or the user's health condition.
  • FIG. 8 is a block diagram showing the detailed structure of the vital sign measurement unit 101 . It is assumed that the vital sign measurement unit 101 is connected to a pulse wave sensor 1 .
  • the pulse wave sensor 1 is a known transparent optical sensor including light emitting elements and light receiving elements, and is intended to measure a pulse wave when mounted on a finger-tip portion.
  • the vital sign measurement unit 101 includes a pulse wave detection unit 1011 , a pulse wave derivative unit 1012 , a component extraction unit 1013 , a component ratio calculation unit 1014 , a component ratio storage unit 1015 , a variance value calculation unit 1016 , a determination unit 1017 , a noise segment removal unit 1018 , and an accumulation unit 1019 .
  • the pulse wave detection unit 1011 detects, as a pulse wave, an output signal from the pulse wave sensor 1 .
  • the pulse wave derivative unit 1012 performs first-order derivative on the pulse wave detected by the pulse wave detection unit 1011 to obtain a velocity plethysmogram.
  • the component extraction unit 1013 extracts the maximum value and the minimum value in each of predetermined time ranges of the velocity plethysmogram obtained by the pulse wave derivative unit 1012 .
  • the component ratio calculation unit 1014 calculates a component ratio by dividing the minimum value by the maximum value of the velocity plethysmogram extracted by the component extraction unit 1013 .
  • the component ratio storage unit 1015 stores the component ratio calculated by the component ratio calculation unit 1014 .
  • the variance value calculation unit 1016 calculates component ratio variance values stored in the component ratio storage unit 1015 . It is assumed here that the variance values are sample variance values, and are calculated using the following expression.
  • the determination unit 1017 determines whether or not the pulse wave contains noise, based on the variance values of the plural component ratios calculated by the variance value calculation unit 1016 .
  • the noise segment removal unit 1018 removes a pulse wave portion corresponding to the noise segment.
  • the accumulation unit 1019 accumulates the data of the pulse wave without the portion corresponding to the noise segment.
  • FIG. 9 shows (i) a solid-line graph representing the maximum value and the minimum value (the minimum value/the maximum value) of the velocity plethysmogram extracted, on a per predetermined time range basis, based on the velocity plethysmogram data affected by the body movements shown in FIG. 5 (Segments A and B are the segments affected by the body movements), and (ii) a broken-line graph representing the ratio of the maximum value and the minimum value (the minimum value/the maximum value) of the velocity plethysmogram extracted, on a per predetermined time range basis, based on the velocity plethysmogram data affected by the change in the thermal sensation shown in FIG. 6 (Segment C is the segment affected by the thermal sensation).
  • the Inventors of the present invention have found that the ratio of the maximum value and the minimum value in the velocity plethysmogram changes significantly in each of Segments A and B affected by the body movements, and that the ratio of the maximum value and the minimum value in the velocity plethysmogram changes slightly in Segment C affected by the change in the thermal sensation. Accordingly, the use of the ratio of the maximum value and the minimum value in the velocity plethysmogram makes it possible to discriminate the change in the pulse wave due to a change in the thermal sensation from noise caused due to the influence of body movements.
  • FIG. 10 shows (i) a solid-line graph representing the variance values of the ratio of the maximum value and the minimum value (the minimum value/the maximum value) of the velocity plethysmogram extracted, on a per predetermined time range basis, based on the velocity plethysmogram data affected by body movements shown in FIG. 5 (Segments A and B are the segments affected by the body movements), and (ii) a broken-line graph representing the variance value of the ratio of the maximum value and the minimum value (the minimum value/the maximum value) of the velocity plethysmogram extracted, on a per predetermined time range basis, based on the velocity plethysmogram data affected by change in the thermal sensation shown in FIG.
  • Segment C is the segment affected by the thermal sensation.
  • the Inventors of the present invention have found that the variance in the ratios of the maximum values and the minimum values in the velocity plethysmogram changes significantly in each of Segments A and B affected by the body movements, and that the variance of the ratios of the maximum values and the minimum values in the velocity plethysmogram changes slightly in Segment C affected by the change in the thermal sensation. Accordingly, the use of the variance of the ratios of the maximum values and the minimum values in the velocity plethysmogram makes it possible to discriminate the change in the pulse wave due to the change in the thermal sensation from noise caused due to the influence of the body movements.
  • FIG. 11 is a flowchart of processing performed by the device control device according to Embodiment 1 of the present invention.
  • the vital sign measurement unit 101 measures and accumulates pulse wave data in time series (S 1 ). This process (S 1 ) is described later in detail.
  • the parameter extraction unit 102 extracts pulse wave amplitude from the time-series pulse wave data measured by the vital sign measurement unit 101 on a predetermined time range basis, and accumulates the pulse wave amplitude (S 2 ).
  • the parameter change amount calculation unit 103 calculates, as a change amount from the starting point, the difference between the value at the predetermined starting time point and the value at a current time in the time-series pulse wave amplitude data extracted by the parameter extraction unit 102 . In addition, the parameter change amount calculation unit 103 calculates, as the previous change amount, the difference between the value at the previous measurement time point and the value at the current time point. The parameter change amount calculation unit 103 outputs the calculated change amount from the starting point and the previous change amount to the change factor determination unit 105 (S 3 ).
  • the parameter change time calculation unit 104 calculates, as change time from the starting point, an elapsed time from the predetermined starting time point to the current time point in the time-series pulse wave amplitude data extracted by the parameter extraction unit 102 , and outputs the change time from the starting point to the change factor determination unit 105 (S 4 ).
  • the change factor determination unit 105 determines the factor of the change in the pulse wave amplitude, based on (i) the change amount from the starting point and the previous change amount outputted by the parameter change amount calculation unit 103 and (ii) the change time from the starting point outputted by the parameter change time calculation unit 104 (S 5 ).
  • the change factor determination unit 105 determines that the factor of the change is the change in the thermal sensation (YES in S 5 )
  • it outputs, to the thermal sensation evaluation unit 108 , the current change amount from the starting point that is information to be used for evaluating the thermal sensation.
  • the change factor determination unit 105 determines that the factor of the change is the change in the health condition (NO in S 5 ), it outputs, to the health condition evaluation unit 109 , the current change amount from the starting point that is information to be used for evaluating the health condition. This determination process (S 5 ) is described later in detail.
  • the thermal sensation evaluation unit 108 evaluates the user's thermal sensation based on the change amount from the starting point outputted by the change factor determination unit 105 , and outputs the evaluation result to the device control unit 107 (S 6 ). In other words, the thermal sensation evaluation unit 108 evaluates the user's thermal sensation based on a code representing the change amount from the starting point. For example, the thermal sensation evaluation unit 108 evaluates that the thermal sensation is shifted to “hot” when the value of the change amount is positive, and that the thermal sensation is shifted to “cold” when the value of the change amount is negative.
  • the thermal sensation evaluation unit 108 evaluates that the thermal sensation is shifted to “hot” when the pulse wave amplitude of the pulse waveform increases, and that the thermal sensation is shifted to “cold” when the pulse wave amplitude of the pulse waveform decreases.
  • thermal sensation based on not the pulse wave amplitude but (i) the maximum value of the pulse wave height, (ii) the waveform component ratio of the waveform of an accelerated plethysmogram (abbreviated as APG) obtained by performing second-order derivative on the pulse waveform, (iii) the amplitude of the accelerated plethysmogram or the pulse rate, and (iv) the change amount in parameters obtainable by performing frequency analysis on a pulse wave interval basis.
  • APG waveform component ratio of the waveform of an accelerated plethysmogram
  • a ratio of low frequency components (0.04 Hz to 0.15 Hz, for example) and high frequency components (0.15 Hz to 0.4 Hz, for example) obtained by dividing the low frequency components by the high frequency components (abbreviated as LF/HF), and evaluate that the thermal sensation is shifted to “discomfort” when the ratio increases and that the thermal sensation is shifted to “comfort” when the ratio decreases.
  • the health condition evaluation unit 109 evaluates the user's health condition based on the change amount from the starting point outputted by the change factor determination unit 105 , and outputs the evaluation result to the device control unit 107 (S 7 ).
  • the fatigue levels include not only a perceived fatigue level but also an unperceived fatigue level.
  • the device control unit 107 controls a predetermined device based on the evaluation result outputted by either the thermal sensation evaluation unit 108 or the health condition evaluation unit 109 (S 8 ). For example, it is also good to perform device control for notifying the user of the evaluation result. In addition, it is also good to perform device control for making better the thermal sensation or the health condition as the evaluation result.
  • FIG. 12 is a flowchart of processing performed by the change factor determination unit 105 according to Embodiment 1 of the present invention.
  • FIG. 13 is a diagram showing a data table used for determining the factor of a change in the amplitude of the pulse wave amplitude stored in the change factor determination unit 105 . The processing shown in FIG. 12 is described below based on the contents of the data table shown in FIG. 13 .
  • the change factor determination unit 105 obtains the change amount from the starting point and the previous change amount from the parameter change amount calculation unit 103 , and obtains the change time from the starting point from the parameter change time calculation unit 104 (S 9 ).
  • the change factor determination unit 105 determines whether or not the absolute value of the change amount from the starting point is greater than a predetermined numerical value (0.1) (S 10 ).
  • the change factor determination unit 105 determines whether or not the absolute value of the previous change amount is smaller than the predetermined numerical value (0.1) (S 11 ).
  • the change factor determination unit 105 waits until the next change amount from the starting point and the previous change amount are obtained, and repeats the processing from S 9 .
  • the change factor determination unit 105 determines whether or not the change time from the starting point is greater than a predetermined value (10 minutes) (S 13 ).
  • the change factor determination unit 105 determines that the factor of the change in the pulse wave amplitude is a change in the thermal sensation as shown in FIG. 13 , and outputs, to the thermal sensation evaluation unit 108 , the current change amount from the starting point that is information to be used for evaluating the thermal sensation (S 12 ).
  • the change factor determination unit 105 determines that the factor of the change in the pulse wave amplitude is a change in the health condition as shown in FIG. 13 , and outputs the current change amount from the starting point that is information to be used for evaluating the health condition to the health condition evaluation unit 109 (S 14 ).
  • the change factor determination unit 105 determines that the factor of the change in the pulse wave amplitude is a change in the thermal sensation, and outputs, to the thermal sensation evaluation unit 108 , the current change amount from the starting point that is information to be used for evaluating the thermal sensation (S 12 ).
  • FIG. 14 shows graphs of changes in the thermal sensation and fatigue level in the case where the environment temperature changes.
  • the horizontal axis shows time. Meanwhile, the vertical axis shows temperatures, thermal sensation levels, and fatigue levels.
  • These graphs show the average values of the thermal sensation levels and the fatigue levels perceived by 10 subjects in the case where the environment temperature changes within a range of approximately 17 to 32 degrees Celsius.
  • the thermal sensation levels are represented as values within a range between ⁇ 3 to +3 inclusive.
  • “+3” denotes the hottest level
  • ⁇ 3” denotes the coldest level.
  • the numerical value increases toward the positive side as the level of hot sensation increases.
  • the fatigue levels fall within the range between 0 and 3 inclusive. “0” indicates that the fatigue level is none, and “3” indicates that the fatigue level is the maximum level.
  • the numerical value increases toward the positive side as the fatigue level increases.
  • the environment temperature is constant during a period from 0 to 24 minutes, starts to change at the 24-minute point, increases to the highest temperature at the 51-minute point, and decreases to the lowest temperature at the 105-minute point. Focusing on the thermal sensation, a change occurs approximately after 3 minutes from the 24-minute point (Point 71 ). In addition, a change occurs approximately after 3 minutes from the 51-minute point (Point 72 ). Further, a change occurs approximately after 6 minutes from the 105-minute point (Point 73 ). Likewise, focusing on the fatigue level, a change occurs approximately after 12 minutes from the 24-minute point (Point 74 ). In addition, a change occurs approximately after 45 minutes from the 51-minute point (Point 75 ).
  • the thermal sensation level responds to a temperature change in a shorter time than in the fatigue level. More specifically, as shown in FIG. 15 , the thermal sensation level starts to change approximately within 12 minutes in response to the temperature change, whereas the fatigue level starts to change approximately after 12 minutes or more in response to the temperature change.
  • the threshold value for the change time from the starting point is determined to be 10 minutes in this embodiment.
  • FIG. 17 is a flowchart of processing performed by the vital sign measurement unit 101 .
  • the pulse wave detection unit 1011 detects an output signal from the pulse wave sensor 1 as a pulse wave (S 201 ).
  • the pulse wave derivative unit 1012 calculates velocity plethysmogram by performing first-order derivative on the pulse wave detected by the pulse wave detection unit 1011 , and stores the velocity plethysmogram in an external memory (S 202 ).
  • the component extraction unit 1013 checks whether or not the maximum value and the minimum value can be extracted from the velocity plethysmogram calculated by the pulse wave derivative unit 1012 (S 203 ).
  • the vital sign measurement unit 101 checks whether or not the vital sign measurement unit 101 satisfies a condition for terminating the current processing (the condition is, for example, an elapse of a specified time and an End operation) (S 213 ), and terminates the processing in the case where the termination condition is satisfied (YES in S 213 ).
  • the pulse wave detection unit 1011 continues the pulse wave detection process (S 201 ).
  • the component extraction unit 1013 extracts the maximum value and the minimum value of the velocity plethysmogram within the predetermined time range (S 204 ).
  • FIG. 18 is a waveform diagram showing temporal changes in the velocity plethysmogram.
  • the horizontal axis shows time
  • the vertical axis shows the magnitude of the velocity plethysmogram.
  • the component extraction unit 1013 extracts, as the maximum value of the velocity plethysmogram, the maximum wave height value (U(n) in FIG. 18 ) in the predetermined time range (T 1 in FIG. 18 ) of the velocity plethysmogram. In addition, the component extraction unit 1013 extracts, as the minimum value of the velocity plethysmogram, the minimum wave height value (S(n) in FIG. 18 ) in a time range temporally backward of the point (U(n) in FIG. 18 ) at which the maximum value has been extracted. It is also good to set the predetermined time range (T 1 in FIG.
  • the determination process (S 203 ) for determining whether or not the maximum value and the minimum value of the velocity plethysmogram can be extracted is performed depending on whether or not the velocity plethysmogram which include all data items in the predetermined time range (T 1 in FIG. 18 ) has already been calculated.
  • the component ratio calculation unit 1014 calculates the component ratio by dividing the minimum value by the maximum value (S 205 ).
  • the minimum value and the maximum value are the values extracted by the component extraction unit 1013 .
  • the component ratio storage unit 1015 stores the component ratio calculated by the component ratio calculation unit 1014 (S 206 ).
  • the variance value calculation unit 1016 checks whether or not the variance values of the component ratios stored in the component ratio storage unit 1015 can be calculated (S 207 ). In the case where the variance values of the component ratios cannot be calculated (NO in S 207 ), the vital sign measurement unit 101 checks whether or not a condition for terminating the processing is satisfied (S 213 ). In the case where the termination condition is satisfied (YES in S 213 ), the vital sign measurement unit 101 terminates the processing. In the case where the termination condition is not satisfied (NO in S 213 ), the pulse wave detection unit 1011 continues the pulse wave detection process (S 201 ).
  • the variance value calculation unit 1016 calculates, as indicators, the variance values of the component ratios (S 208 ).
  • the i-th calculated component ratio is F(i)
  • the number of components F to be used for calculating the variance values is k.
  • the n-th variance value is calculated based on the component ratios from F(n) to F(n+k)
  • the n+1-th variance value is calculated based on the component ratios from F(n+1) to F(k+n+1) shifted by 1 from the respective components ratios used for the n-th variance value.
  • the process (S 207 ) for determining whether or not the variance values can be calculated is performed depending on whether or not the component ratios stored in the component ratio storage unit 1015 is sufficient in number in order to calculate the variance values.
  • the determination unit 1017 determines whether or not the variance values calculated by the variance value calculation unit 1016 fall within the range predetermined for variance values (the range is 0.00 to 0.01, for example) (S 209 ).
  • the determination unit 1017 determines that the detected pulse noise does not include noise, and the noise segment removal unit 1018 outputs the data indicating the pulse wave to the accumulation unit 1019 without performing noise removal (S 210 ).
  • the determination unit 1017 determines that the detected pulse wave includes noise, and the noise segment removal unit 1018 removes the pulse wave portion corresponding to the noise segment and outputs the data indicating the pulse wave which has been subjected to the noise removal to the accumulation unit 1019 (S 211 ).
  • the accumulation unit 1019 accumulates the pulse wave data outputted by the noise segment removal unit 1018 (S 212 ).
  • the vital sign measurement unit 101 checks whether or not a condition for terminating the current processing is satisfied (S 213 ). In the case where the termination condition is satisfied (YES in S 213 ), the processing is terminated. In the case where the termination condition is not satisfied (NO in S 213 ), the pulse wave detection unit 1011 continues the pulse wave detection process (S 201 ).
  • FIG. 19 is a diagram for illustrating the starting position of the noise segment
  • FIG. 20 shows a diagram for illustrating the ending position of the noise segment.
  • FIG. 19 and FIG. 20 is a graph representing the waveform of the velocity plethysmogram.
  • the horizontal axis shows time, and the vertical axis shows the values of velocity plethysmogram.
  • the variance value calculation unit 1016 calculates the variance value in each of the consecutive time segments 1001 , 1002 , and 1003 .
  • the variance value in each of the time segments is calculated based on three temporally consecutive component ratios.
  • the variance values in the respective time segments 1001 and 1002 fall within the range predetermined for variance values
  • the variance value in the time segment 1003 does not fall within the range predetermined for variance values.
  • the noise segment removal unit 1018 determines, as the starting position of the noise segment, the position of the second component ratio (in the diagram, the position indicates the corresponding velocity plethysmogram) among the three component ratios included in the time segment 1003 .
  • the variance value calculation unit 1016 calculates the variance values in the consecutive time segments 1004 and 1005 .
  • the variance value in each of the time segments is calculated based on three temporally consecutive component ratios.
  • the variance value in the time segment 1004 does not fall within the range predetermined for variance values
  • the variance value in the time segment 1005 falls within the range predetermined for variance values.
  • the variance values in the time segments prior to the time segment 1004 do not fall within the range predetermined for the variance values.
  • the noise segment removal unit 1018 determines, as the ending position of the noise segment, the position of the second component ratio (in the diagram, the position indicates the corresponding velocity plethysmogram) among the three component ratios included in the time segment 1005 .
  • the method for determining the starting position and the ending position of the noise segment is not limited to this. For example, it is also good to determine, as the starting position of the noise segment, the position of the first component ratio or the position of the third component ratio in the time segment determined to be outside the range predetermined for variance values. Otherwise, it is also good to determine, as the ending position of the noise segment, the position of the first component ratio or the position of the third component ratio in the time segment determined to be within the range predetermined for variance values. Further, the number of component ratios used for calculating a variance value is not limited to three, any other number is possible.
  • FIG. 21 is a diagram for illustrating removal of noise from pulse wave data.
  • FIG. 21( a ) is a graph representing temporal changes in the amplitude value of Wave a (described later) that is a first wave of the accelerated plethysmogram which has not yet been subjected to noise removal.
  • FIG. 21( b ) is a graph representing temporal changes in the amplitude value of Wave a in the accelerated plethysmogram which has been subjected to the noise removal.
  • the horizontal axis shows time
  • the vertical axis shows the amplitude values of Wave a in the accelerated plethysmogram.
  • the variance value (variance value of component ratios) of the amplitude values of Wave a in Segment 1203 is smaller than those in the other segments.
  • Segment 1213 corresponding to Segment 1203 is not regarded as a noise segment, and no noise removal is performed on Segment 1213 .
  • the example in FIG. 21 shows temporal changes in the amplitude values of Wave a in the accelerated plethysmogram. Likewise, noise removal is performed on the corresponding positions of the pulse wave data.
  • FIG. 22 is a diagram showing an example of the waveform of the velocity pulse wave.
  • the accelerated plethysmogram includes Wave a, Wave b, Wave c, Wave d, and Wave e.
  • the apex A of Wave a matches the starting point of the diastolic wave of the finger-tip plethysmogram (abbreviated as PTG), and thus the required time from Apex A to Apex E matches the length of systolic time axis of the user's heart.
  • Wave a is a positive wave that is upwardly convex with respect to the baseline
  • Wave b is a negative wave that is downwardly convex with respect to the baseline
  • Wave c, Wave d, and Wave e are element waves that change between positive and negative depending on user's physiological conditions, and are highly correlated with the user's age.
  • the parameter extraction unit 102 extracts parameter vales which have been subjected to the noise removal.
  • the parameter change amount calculation unit 103 calculates the change amount from the starting point and the previous change amount based on the parameter values which have been subjected to the noise removal. For example, it is also good to calculate the change amount from the starting point only when the parameter values at the starting time point and the current time point have been obtained, and to calculate the previous change amount only when the parameter values at the previous continuation time point and the parameter values at the current time point have been obtained.
  • the device control device when a user's pulse wave changes, it is possible to determine the factor of the change in the pulse wave taking into account the time required for the change in addition to the change amount in the pulse wave. In other words, it is possible to discriminate the factor of the change in the pulse wave, that is, determine whether the change is due to a change in the user's thermal sensation or a change in the user's health condition. In addition, it is also possible to evaluate the user's thermal sensation or health condition based on the factor of the change. This prevents device control based on an erroneous evaluation result in the system for obtaining the user's pulse wave and feeding back information about the pulse wave, and makes it possible to reliably present the user status and perform device control to make better the user status.
  • Embodiment 2 of the present invention.
  • the same elements as those of the device control device according to Embodiment 1 are assigned with the same numerical references.
  • the functions and names are also the same, and thus no detailed descriptions are repeated here.
  • FIG. 23 is a block diagram showing the structure of a device control device according to Embodiment 2 of the present invention.
  • the device control device shown in FIG. 23 is configured with known computers for example, and includes a vital sign measurement unit 101 , a parameter extraction unit 102 , a determination unit 520 , and a control unit 130 . These processing units function when the program is executed by a CPU of a computer storing an installed device control program designed according to this embodiment.
  • the determination unit 520 is a processing unit for determining the factor of a change in the pulse wave data using parameter values extracted by the parameter extraction unit 102 .
  • the determination unit 520 includes a parameter change amount calculation unit 103 , an environment temperature measurement unit 504 , a unit 505 for calculating a temperature change amount from a starting point, and a change factor determination unit 506 .
  • the environment temperature measurement unit 504 measures and accumulates environment temperature data.
  • the unit 505 for calculating a temperature change amount from a starting point calculates, as a change amount from a starting point, the difference between the value at a predetermined starting time point and the value at a current time point in the environment temperature data measured by the environment temperature measurement unit 504 , and outputs the current change amount from the starting point to the change factor determination unit 506 .
  • the change factor determination unit 506 determines the factor of the change in the pulse wave amplitude (the factor is, for example, the influence of a thermal sensation or the influence of a health condition), based on (i) the change amount from the starting point calculated by the parameter change amount calculation unit 103 and (ii) the temperature change amount from the starting point calculated by the unit 505 for calculating a temperature change amount from the starting point. Based on the determined factor, the change factor determination unit 506 selects the best evaluation unit from among the thermal sensation evaluation unit 108 and the health condition evaluation unit 109 included in the status evaluation unit 106 , and outputs, to the selected evaluation unit, the current change amount from the starting point that is information to be used for evaluating the current status.
  • the factor is, for example, the influence of a thermal sensation or the influence of a health condition
  • FIG. 24 is a flowchart of processing performed by the device control device according to Embodiment 2 of the present invention.
  • the device control device executes the processes from S 1 to S 3 as in Embodiment 1.
  • the unit 505 for calculating a temperature change amount from a starting point calculates, as the change amount from the starting point, the difference between the value at a predetermined starting time point and the value at a current time point in the environment temperature data measured by the environment temperature measurement unit 504 , and outputs the current change amount from the starting point to the change factor determination unit 506 (S 18 ).
  • the change factor determination unit 506 determines the factor of the change in the pulse wave amplitude based on the change amount from the starting point calculated by the parameter change amount calculation unit 103 and the temperature change amount from the starting point outputted by the unit 505 for calculating a temperature change amount from a starting point (S 19 ).
  • the change factor determination unit 506 determines that the factor of the change is a change in the thermal sensation (YES in S 19 )
  • it outputs, to the thermal sensation evaluation unit 108 , the current change amount from the starting point that is information to be used for evaluating the thermal sensation.
  • the change factor determination unit 506 determines that the factor of the change is a change in the health condition (NO in S 19 ), it outputs, to the health condition evaluation unit 109 , the current change amount from the starting point that is information to be used for evaluating the health condition. This determination process (S 19 ) is described later in detail.
  • the device control device performs device control by executing the processes from S 6 to S 8 as in Embodiment 1.
  • FIG. 25 is a flowchart of processing performed by the change factor determination unit 506 according to Embodiment 2 of the present invention.
  • FIG. 26 is a diagram showing a data table used for determining the factor of the change in the amplitude of the pulse wave stored in the change factor determination unit 506 . The processing shown in FIG. 25 is described below based on the contents of the data table shown in FIG. 26 .
  • the change factor determination unit 506 obtains the change amount from the starting point from the parameter change amount calculation unit 103 , and obtains the temperature change amount from the starting point from the unit 505 for calculating the temperature change amount from the starting point (S 23 ).
  • the change factor determination unit 506 determines whether or not the absolute value of the change amount from the starting point is greater than a predetermined numerical value (0.1) (S 24 ).
  • 0.1 a predetermined numerical value
  • the change factor determination unit 506 determines whether or not the absolute value of the temperature change amount from the starting point is greater than the predetermined numerical value (3 degrees Celsius) (S 25 ).
  • the change factor determination unit 506 waits until the next change amount from the starting point and the temperature change amount from the starting point are obtained, and repeats the processing from S 23 .
  • the change factor determination unit 506 determines that the factor of the change in the amplitude of the pulse wave as shown in FIG. 26 is a change in the thermal sensation, and outputs, to the thermal sensation evaluation unit 108 , the current change amount from the starting point that is information to be used for evaluating the thermal sensation (S 12 ).
  • the change factor determination unit 506 determines that the factor of the change in the amplitude of the pulse wave as shown in FIG. 26 is a change in the health condition, and outputs, to the health condition evaluation unit 109 , the current change amount from the starting point that is information to be used for evaluating the health condition (S 14 ).
  • the thermal sensation changes significantly for the first time at Point 71 .
  • the change amount from the temperature at the 24-minute time point from the time point 71 is approximately 0.5 degrees Celsius.
  • the fatigue level changes significantly for the first time at Point 74 .
  • the change amount from the temperature at the 24-minute time point from the time point 74 is approximately 3.6 degrees Celsius.
  • the thermal sensation is more susceptible to the temperature change than the fatigue level, and the border is determined to be a range between 0.5 degrees Celsius and 3.6 degrees Celsius inclusive.
  • the threshold value for the temperature change amount from the starting point is determined to be 3 degrees Celsius in this embodiment.
  • the device control device when a user's pulse wave changes, it is possible to determine the factor of the change in the pulse wave taking into account the change amount in the environment temperature in addition to the change amount in the pulse wave. In other words, it is possible to discriminate the factor of the change in the pulse wave, that is, determine whether the change is due to a change in the thermal sensation or a change in the health condition. In addition, it is also possible to evaluate the user's thermal sensation or health condition based on the change factor. This prevents device control based on an erroneous evaluation result in the system for obtaining the user's pulse wave and feeding back information about the pulse wave, and makes it possible to reliably present the user status and perform device control to make better the user status.
  • Embodiment 3 of the present invention.
  • the same elements as those of the device control device according to Embodiment 1 are assigned with the same numerical references.
  • the functions and names are also the same, and thus no detailed descriptions are repeated here.
  • FIG. 28 is a block diagram showing the structure of a device control device according to Embodiment 3 of the present invention.
  • the device control device shown in FIG. 28 is configured with known computers for example, and includes a vital sign measurement unit 101 , a parameter extraction unit 102 , a determination unit 920 , and a control unit 130 . These processing units function when the program is executed by a CPU of a computer storing an installed device control program designed according to this embodiment.
  • the determination unit 920 is a processing unit for determining the factor of a change in the pulse wave data using parameter values extracted by the parameter extraction unit 102 .
  • the determination unit 120 includes a parameter change amount calculation unit 103 , a parameter change amount integration unit 904 , and a change factor determination unit 905 .
  • the parameter change amount integration unit 904 calculates, as an integration value of change amounts each from a point immediately before a current point (a previous point), an integration value of the change amounts from a predetermined starting time point to a current time point in the time-series data of the pulse wave amplitude extracted by the parameter extraction unit 102 , and outputs, to the change factor determination unit 905 , the integration value of the change amounts each from the previous point.
  • the change factor determination unit 905 determines the factor of the change in the pulse wave amplitude (the factor is, for example, the influence of a thermal sensation or the influence of a health condition), based on (i) the change amount from the starting point calculated by the parameter change amount calculation unit 103 and (ii) the integration value of the change amounts each from the previous point calculated by the parameter change amount integration unit 904 . Based on the determined factor, the change factor determination unit 905 selects the best evaluation unit from among the thermal sensation evaluation unit 108 and the health condition evaluation unit 109 included in the status evaluation unit 106 , and outputs, to the selected evaluation unit, the current change amount from the starting point that is information to be used for evaluating the current status.
  • the factor is, for example, the influence of a thermal sensation or the influence of a health condition
  • FIG. 29 is a flowchart of processing performed by the device control device according to Embodiment 3 of the present invention.
  • the device control device executes the processes from S 1 to S 3 as in Embodiment 1.
  • the parameter change amount integration unit 904 calculates, as an integration value of change amounts each from the previous point, an integration value of the change amounts from a predetermined starting time point to a current time point in the time-series data of the pulse wave amplitude extracted by the parameter extraction unit 102 , and output, to the change factor determination unit 905 , the integration value of the change amounts each from the previous point (S 31 ).
  • the change factor determination unit 905 determines the factor of the change in the pulse wave amplitude based on (i) the change amount from the starting point outputted by the parameter change amount calculation unit 103 and (ii) the integration value of the change amounts each from the previous point outputted by the parameter change amount integration unit 904 (S 32 ).
  • the change factor determination unit 905 determines that the factor of the change is a change in the thermal sensation (YES in S 32 )
  • it outputs, to the thermal sensation evaluation unit 108 , the current change amount from the starting point that is information to be used for evaluating the thermal sensation.
  • the change factor determination unit 905 determines that the factor of the change is a change in the health condition (NO in S 32 ), it outputs, to the health condition evaluation unit 109 , the current change amount from the starting point that is information to be used for evaluating the health condition. This determination process (S 32 ) is described later in detail.
  • the device control device performs device control by executing the processes from S 6 to S 8 as in Embodiment 1.
  • FIG. 30 is a flowchart of processing performed by the change factor determination unit 905 according to Embodiment 3 of the present invention.
  • FIG. 31 is a diagram showing a data table used for determining the factor of the change in the amplitude of the pulse wave stored in the change factor determination unit 905 . The processing shown in FIG. 30 is described below based on the contents of the data table shown in FIG. 31 .
  • the change factor determination unit 905 obtains the change amount from the starting point from the parameter change amount calculation unit 103 , and obtains the integration value of the change amounts each from the previous point from the parameter change amount integration unit 904 (S 36 ).
  • the change factor determination unit 905 determines whether or not the absolute value of the change amount from the starting point is greater than a predetermined numerical value (0.1) (S 37 ).
  • a predetermined numerical value 0.1
  • the change factor determination unit 905 determines whether or not the integration value of the change amounts each from the previous point is greater than a predetermined numerical value (1) (S 38 ).
  • the change factor determination unit 905 waits until the next change amount from the starting point and the next integration value of the change amounts each from the previous point are obtained, and repeats the processing from S 36 .
  • the change factor determination unit 905 determines that the factor of the change in the pulse wave amplitude is a change in the health condition as shown in FIG. 31 , and outputs, to the health condition evaluation unit 109 , the current change amount from the starting point that is information to be used for evaluating the health condition (S 14 ).
  • the change factor determination unit 905 determines that the factor of the change in the pulse wave amplitude is change in the thermal sensation as shown in FIG. 31 , and outputs, to the thermal sensation evaluation unit 108 , the current change amount from the starting point that is information to be used for evaluating the thermal sensation (S 12 ).
  • the device control device when a user's pulse wave changes, it is possible to determine the factor of the change in the pulse wave taking into account the integration value of the change amounts in addition to the change amount in the pulse wave. In other words, it is possible to discriminate the factor of the change in the pulse wave, that is, determine whether the change is due to a change in the thermal sensation or a change in the health condition. In addition, it is also possible to evaluate the user's thermal sensation or health condition based on the change factor. This prevents device control based on an erroneous evaluation result in the system for obtaining the user's pulse wave and feeding back information about the pulse wave, and makes it possible to reliably present the user status and perform device control to make the user status better.
  • Embodiment 4 of the present invention.
  • the same elements as those of the device control device according to Embodiment 1 are assigned with the same numerical references.
  • the functions and names are also the same, and thus no detailed descriptions are repeated here.
  • the device control device is intended to control an on-vehicle device.
  • FIG. 32 is a block diagram showing the structure of the device control device according to Embodiment 4 of the present invention.
  • the device control device shown in FIG. 32 is configured with known computers for example, and includes a superior control unit 1111 , a vehicle information obtainment unit 1112 , a vital sign measurement unit 1101 , a parameter extraction unit 102 , a determination unit 1120 , and a control unit 1130 .
  • These processing units function when the program is executed by a CPU of a computer storing an installed device control program designed according to this embodiment.
  • the vehicle information obtainment unit 1112 obtains information about the status of a vehicle.
  • the vehicle information obtainment unit 1112 obtains information such as information indicating whether the vehicle is running or stopped, information about handle operations such as handle operation acceleration, the running speed of the vehicle, and traffic jam information.
  • the superior control unit 1111 directs the vital sign measurement unit 1101 to start and end obtainment of pulse wave data, based on information about the statuses of the vehicle obtained by the vehicle information obtainment unit 1112 .
  • the superior control unit 1111 may direct the vital sign measurement unit 1101 to start the obtainment of the pulse wave data when the engine of the vehicle is turned on, and to end the obtainment of the pulse wave data when the engine of the vehicle is turned off.
  • the vital sign measurement unit 1101 starts and ends the processing under control of the superior control unit 1111 .
  • the vital sign measurement unit 1101 functions in the same manner as the vital sign measurement unit 101 described in Embodiment 1. In other words, the vital sign measurement unit 1101 obtains time-series pulse wave data of a finger-tip pulse wave of a driver.
  • the determination unit 1120 is a processing unit for determining the factor of a change in the pulse data using parameter values extracted by the parameter extraction unit 102 , and includes the parameter change amount calculation unit 103 and a change factor determination unit 1105 .
  • the change factor determination unit 1105 determines the factor of the change in the pulse wave amplitude (the factor is, for example, the influence of a thermal sensation or the influence of a health condition), based on (i) the change amount from the starting point calculated by the parameter change amount calculation unit 103 and (ii) the information about the status of the vehicle obtained by the vehicle information obtainment unit 1112 . Based on the determined factor, the change factor determination unit 1105 selects the best evaluation unit from among a thermal sensation evaluation unit 108 and a fatigue evaluation unit 1109 included in a later-described status evaluation unit 1116 , and outputs, to the selected evaluation unit, the current change amount from the starting point that is information to be used for evaluating the current status.
  • the factor is, for example, the influence of a thermal sensation or the influence of a health condition
  • the control unit 1130 is a processing unit for performing device control based on the determination result made by the change factor determination unit 1105 , and includes a status evaluation unit 1116 and a device control unit 1117 .
  • the status evaluation unit 1116 is a processing unit for evaluating the status of the driver based on the change amount from the starting point in the pulse wave amplitude outputted by the change factor determination unit 1105 , and includes a fatigue evaluation unit 1109 and the thermal sensation evaluation unit 108 .
  • the fatigue evaluation unit 1109 evaluates the fatigue level of the user based on the change amount from the starting point in the pulse wave amplitude outputted by the change factor determination unit 1105 , and outputs the evaluation result to a later-described fatigue related device control unit 1113 of the control unit 1130 .
  • the thermal sensation evaluation unit 108 evaluates the user's thermal sensation based on the change amount from the starting point in the pulse wave amplitude outputted by the change factor determination unit 1105 , and outputs the evaluation result to a later-described thermal sensation related device control unit 1114 included in the control unit 1130 .
  • the device control unit 1117 is a processing unit for controlling an on-vehicle device based on the evaluation result made by the fatigue evaluation unit 1109 or the thermal sensation evaluation unit 108 , and includes the fatigue related device control unit 1113 and the thermal sensation related device control unit 1114 .
  • the fatigue related device control unit 1113 performs device control for lowering the fatigue level of the driver based on the driver's fatigue level evaluated by the fatigue evaluation unit 1109 .
  • the thermal sensation related device control unit 1114 Based on the driver's thermal sensation evaluated by the thermal sensation evaluation unit 108 , the thermal sensation related device control unit 1114 performs device control for making better the driver's thermal sensation.
  • FIG. 33 is a block diagram showing the detailed structure of the vital sign measurement unit 1101 . It is assumed that the vital sign measurement unit 1101 is connected to the pulse wave sensor 1 . It is assumed that the pulse wave sensor 1 is provided on the handle of the vehicle, and measures the pulse wave of the driver while the driver is grasping the handle.
  • the vital sign measurement unit 1101 is basically the same as the vital sign measurement unit 101 shown in FIG. 8 , but is different in including a pulse wave detection unit 1121 instead of the pulse wave detection unit 1011 .
  • the pulse wave detection unit 1121 is connected to the superior control unit 1111 and the pulse wave sensor 1 .
  • the pulse wave detection unit 1121 keeps detection of output signals as a pulse wave from the pulse wave sensor 1 during a period from when the superior control unit 1111 directs the start of obtainment of the pulse data to when the superior control unit 1111 directs the end of the obtainment of the pulse data.
  • FIG. 34 is a flowchart of processing performed by the device control device according to Embodiment 4 of the present invention.
  • the superior control unit 1111 determines whether or not to measure the pulse wave data based on the information about the status of the vehicle obtained by the vehicle information obtainment unit 1112 (S 41 ). For example, when the superior control unit 1111 obtains, from the vehicle information obtainment unit 1112 , information indicating that the engine of the vehicle is turned on, the superior control unit 1111 determines to start measurement of the pulse wave data. In contrast, when the superior control unit 1111 obtains, from the vehicle information obtainment unit 1112 , information indicating that the engine of the vehicle is turned off, the superior control unit 1111 determines to end the measurement of the pulse wave data.
  • the superior control unit 1111 determines to start measurement of the pulse wave data (YES in S 41 )
  • the superior control unit 1111 directs the vital sign measurement unit 1101 to start obtainment of the pulse wave data.
  • the superior control unit 1111 determines to end the measurement of the pulse wave data (NO in S 41 )
  • the superior control unit 1111 directs the vital sign measurement unit 1101 to end the obtainment of the pulse wave data.
  • the processing is terminated.
  • the superior control unit 1111 directs the vital sign measurement unit 1101 to start obtainment of the pulse wave data (YES in S 41 ), the vital sign measurement unit 1101 that received the direction measures and accumulates pulse wave data of the driver in time series (S 42 ).
  • This process (S 42 ) is the same as the measurement and accumulation process (S 1 ) of the time-series pulse wave data described in Embodiment 1. Therefore, no detailed description is repeated here.
  • the parameter extraction unit 102 extracts the pulse wave amplitude, on a certain time range basis, from the time-series pulse wave data measured by the vital sign measurement unit 1101 (S 2 ).
  • the parameter change amount calculation unit 103 calculates, as a change amount from the starting point, the difference between a value at the predetermined starting time point and the value at a current time point in the time-series pulse wave amplitude data extracted by the parameter extraction unit 102 . In addition, the parameter change amount calculation unit 103 calculates, as a previous change amount, the difference between the value at a previous measurement time point and the value at the current time point. The parameter change amount calculation unit 103 outputs the calculated change amount from the starting point and the calculated previous change amount to the change factor determination unit 1105 (S 3 ).
  • the vehicle information obtainment unit 1112 obtains the data of handle operation performed by the driver, and outputs the obtained handle operation data to the change factor determination unit 1105 (S 43 ). More specifically, the vehicle information obtainment unit 1112 obtains, as the handle operation data, the ratio of time during which the handle operation acceleration (x-y two axis resultant force) exceeds a predetermined value (120 mG, for example) in a period from the predetermined starting time point to a current time point, and outputs the obtained ratio to the change factor determination unit 1105 .
  • a predetermined value 120 mG, for example
  • the change factor determination unit 1105 determines the factor of the change in the pulse wave amplitude based on the change amount from the starting point outputted by the parameter change amount calculation unit 103 and the handle operation data outputted by the vehicle information obtainment unit 1112 (S 44 ).
  • the change factor determination unit 1105 determines that the factor of the change is a change in the thermal sensation (YES in S 44 )
  • it outputs, to the thermal sensation evaluation unit 108 , the current change amount from the starting point that is information to be used for evaluating the thermal sensation.
  • the change factor determination unit 1105 determines that the factor of the change is a change in the fatigue level (NO in S 44 ), it outputs, to the fatigue evaluation unit 1109 , the current change amount from the starting point that is information to be used for evaluating the fatigue level. This determination process (S 44 ) is described later in detail.
  • the thermal sensation evaluation unit 108 evaluates the user's thermal sensation based on the change amount from the starting point outputted by the change factor determination unit 1105 , and outputs the evaluation result to the thermal sensation related device control unit 1114 (S 6 ).
  • the method for evaluating thermal sensation is the same as in Embodiment 1, and thus no detailed description is repeated here.
  • the thermal sensation related device control unit 1114 performs device control for making better the thermal sensation based on the thermal sensation evaluation result outputted by the thermal sensation evaluation unit 108 (S 45 ).
  • the fatigue evaluation unit 1109 evaluates the user's fatigue level based on the change amount from the starting point outputted by the change factor determination unit 1105 , and outputs the evaluation result to the fatigue related device control unit 1113 (S 46 ).
  • the method for evaluating a fatigue level is the same as in Embodiment 1, and thus no detailed description is repeated here.
  • the fatigue related device control unit 1113 Based on the evaluation result of the fatigue level outputted by the fatigue evaluation unit 1109 (S 47 ), the fatigue related device control unit 1113 performs device control for reducing the fatigue level.
  • FIG. 35 is a flowchart of the processing performed by the change factor determination unit 1105 according to Embodiment 4 of the present invention.
  • FIG. 36 is a diagram showing a data table used for determining the factor of the change in the amplitude of the pulse wave stored in the change factor determination unit 1105 . The processing shown in FIG. 35 is described below based on the contents of the data table shown in FIG. 36 .
  • the change factor determination unit 1105 obtains the change amount from the starting point from the parameter change amount calculation unit 103 (S 51 ). In addition, the change factor determination unit 1105 obtains the handle operation data from the vehicle information obtainment unit 1112 (S 52 ). The change factor determination unit 1105 determines whether or not the absolute value of the change amount from the starting point is greater than a predetermined numerical value (0.1)(S 53 ). When the absolute value of the change amount from the starting point is not greater than 0.1 (NO in S 53 ), the change factor determination unit 1105 waits until the next change amount from the starting point and the next handle operation data are obtained, and repeats the process S 51 and the following processes from S 52 .
  • the change factor determination unit 1105 determines whether or not the handle operation data is greater than a predetermined numerical value (15%) (S 54 ). When the absolute value of the handle operation data is greater than 15% (YES in S 54 ), the change factor determination unit 1105 determines that the factor of the change in the pulse wave amplitude is a change in the driver's fatigue level as shown in FIG. 36 , and outputs, to the fatigue evaluation unit 1109 , the current change amount from the starting point that is information to be used for evaluating the fatigue level (S 55 ).
  • the change factor determination unit 1105 determines that the factor of the change in the pulse wave amplitude is a change in the driver's thermal sensation as shown in FIG. 36 , and outputs, to the thermal sensation evaluation unit 108 , the current change amount from the starting point that is information to be used for evaluating the thermal sensation (S 56 ).
  • the threshold value for the handle operation data is determined to be 15%.
  • FIG. 38 is a flowchart of processing executed by the thermal sensation related device control unit 1114 .
  • the thermal sensation related device control unit 1114 obtains the evaluation result of the thermal sensation from the thermal sensation evaluation unit 108 (S 61 ).
  • the thermal sensation related device control unit 1114 determines the control details corresponding to the obtained thermal sensation evaluation result (S 62 ).
  • the control details determined in the case where it is evaluated that the thermal sensation is shifted to “hot” include to lower the temperature of a warm or cool heat output device such as an air conditioner, to lower the temperature of a device for outputting air flow such as cool wind or warm wind, and to increase the air flow.
  • control details determined in the case where it is evaluated that the thermal sensation is shifted to “cold” include to raise the temperature of the warm or cool heat output device such as the air conditioner, to raise the temperature of the device for outputting air flow such as cool wind or warm wind, and to decrease the air flow.
  • the thermal sensation related device control unit 1114 performs device control according to the determined control details (S 63 ).
  • FIG. 39 is a flowchart of the processing executed by the fatigue related device control unit 1113 .
  • the fatigue related device control unit 1113 obtains the evaluation result of the fatigue level from the fatigue evaluation unit 1109 (S 64 ).
  • the fatigue related device control unit 1113 determines the control details corresponding to the obtained fatigue level evaluation result (S 65 ).
  • the control details in the case where it is evaluated that the fatigue level is on the increase include causing a massage device to operate, causing a device for outputting oxygen or negative ions to operate, causing a navigation system to lead the vehicle to nearby woods.
  • the vehicle information obtainment unit 1112 obtains information indicating that the vehicle is stopped (YES in S 66 )
  • the fatigue related device control unit 1113 performs device control according to the determined control details (S 67 ).
  • Performing device control when the vehicle is stopped and not performing device control while the vehicle is running makes it possible, for example, to prevent the massage device from operating during the driving and triggering a handle operation error and prevent a navigation system from misleading the vehicle to a place different from a destination. This allows the driver to continue safety driving to the destination.
  • the device control device when a user's pulse wave changes, it is possible to determine the factor of the change in the pulse wave taking into account the handle operation data in addition to the change amount in the pulse wave. In other words, it is possible to discriminate the factor of the change in the pulse wave, that is, determine whether the change is due to a change in the thermal sensation or a change in the fatigue level. In addition, it is also possible to evaluate the user's thermal sensation or fatigue level based on the change factor. This prevents device control based on an erroneous evaluation result in the system for obtaining the user's pulse wave and feeding back information about the pulse wave, and makes it possible to reliably present the user status and perform device control to make the user status better. In a particular situation where the user drives the vehicle, the most appropriate device control can be performed. This allows the user to drive the vehicle more comfortably and safely.
  • Embodiment 5 of the present invention.
  • the same elements as those of the device control device according to Embodiments 1 to 4 are assigned with the same numerical references.
  • the device control device is intended to control an on-vehicle device.
  • FIG. 40 is a block diagram showing the structure of the device control device according to Embodiment 5 of the present invention.
  • the device control device shown in FIG. 40 is configured with known computers for example, and includes a superior control unit 1111 , a vehicle information obtainment unit 1112 , a vital sign measurement unit 1101 , a parameter extraction unit 102 , a determination unit 1220 , and a control unit 1130 . These processing units function when the program is executed by a CPU of a computer storing an installed device control program designed according to this embodiment.
  • the device control device according to Embodiment 5 includes a determination unit 1220 instead of the determination unit 1120 in the same structure as in the device control device according to Embodiment 4 shown in FIG. 32 . As for the other elements, the device control device according to Embodiment 5 is the same as the device shown in FIG. 32 .
  • the determination unit 1220 includes the parameter change amount calculation unit 103 , the parameter change time calculation unit 104 , and a change factor determination unit 1205 .
  • the change factor determination unit 1205 determines the factor of the change in the pulse wave amplitude (the factor is, for example, the influence of a thermal sensation or the influence of a health condition), based on (i) the change amount from the starting point and the previous change amount calculated by the parameter change amount calculation unit 103 and (ii) the change time from the starting point calculated by the parameter change time calculation unit 104 , and (iii) the information about the status of the vehicle obtained by the vehicle information obtainment unit 1112 .
  • the change factor determination unit 1205 selects the best evaluation unit from among a thermal sensation evaluation unit 108 and a fatigue evaluation unit 1109 included in the status evaluation unit 1116 , and outputs, to the selected evaluation unit, the current change amount from the starting point that is information to be used for evaluating the current user status.
  • FIG. 41 is a flowchart of processing performed by the device control device according to Embodiment 5 of the present invention.
  • the device control device executes the same processes S 41 , S 42 , S 2 , S 3 , and S 43 as in Embodiment 4. Meanwhile, the parameter change time calculation unit 104 calculates, as the change time from the starting point, an elapsed time from the predetermined starting time point to the current time point in the time-series pulse wave amplitude data extracted by the parameter extraction unit 102 , and outputs the current change time from the starting point to the change factor determination unit 1205 (S 4 ).
  • the change factor determination unit 1205 determines the factor of the change in the pulse wave amplitude, based on (i) the change amount from the starting point and the previous change amount outputted by the parameter change amount calculation unit 103 , (ii) the change time from the starting point outputted by the parameter change time calculation unit 104 , and (iii) the handle operation data outputted by the vehicle information obtainment unit 1112 (S 71 ).
  • the change factor determination unit 1205 determines that the factor of the change is a change in the thermal sensation (YES in S 71 ), it outputs, to the thermal sensation evaluation unit 108 , the current change amount from the starting point that is information to be used for evaluating the thermal sensation.
  • the change factor determination unit 1205 determines that the factor of the change is a change in the fatigue level (NO in S 71 ), it outputs, to the fatigue evaluation unit 1109 , the current change amount from the starting point that is information to be used for evaluating the fatigue. This determination process (S 71 ) is described later in detail.
  • the device control device executes the same processes of S 6 and S 45 to S 47 as in Embodiment 4.
  • FIG. 42 is a flowchart of the processing performed by the change factor determination unit 1205 according to Embodiment 5 of the present invention.
  • the change factor determination unit 1205 determines the factor of the change in the pulse wave amplitude using the data table shown in FIG. 13 and the data table shown in FIG. 36 .
  • the processing shown in FIG. 42 is described below based on the contents of the data table shown in FIG. 13 and FIG. 36 .
  • This processing is a combination of the processing executed by the change factor determination unit 105 according to Embodiment 1 shown in FIG. 12 and the processing executed by the change factor determination unit 1105 according to Embodiment 4 shown in FIG. 35 .
  • the change factor determination unit 1205 obtains the change amount from the starting point and the previous change amount from the parameter change amount calculation unit 103 , and obtains the change time from the starting point from the parameter change time calculation unit 104 (S 81 ). In addition, the change factor determination unit 1205 obtains the handle operation data from the vehicle information obtainment unit 1112 (S 52 ).
  • the change factor determination unit 1205 determines whether or not the absolute value of the change amount from the starting point is greater than a predetermined numerical value (0.1)(S 82 ). When the absolute value of the change amount from the starting point is not greater than 0.1 (NO in S 82 ), the change factor determination unit 105 waits until the next change amount from the starting point and the previous change amount are obtained, and repeats the process S 81 and the processes from S 52 .
  • the change factor determination unit 1205 determines whether or not the absolute value of the previous change amount is smaller than the predetermined numerical value (0.1) (S 83 ).
  • the change factor determination unit 1205 determines whether or not the change time from the starting point is greater than a predetermined value (10 minutes) (S 84 ). When the change time from the starting point is greater than 10 minutes (YES in S 84 ), the change factor determination unit 1205 determines that the factor of the change in the pulse wave amplitude is a fatigue level (a health condition) as shown in FIG. 13 , and outputs, to the fatigue evaluation unit 1109 , the current change amount from the starting point that is information to be used for evaluating the fatigue level (S 55 ).
  • the change factor determination unit 1205 determines that the factor of the change in the pulse wave amplitude is a change in the thermal sensation, and outputs, to the thermal sensation evaluation unit 108 , the current change amount from the starting point that is information to be used for evaluating the thermal sensation (S 56 ).
  • the change factor determination unit 1205 determines whether or not the handle operation data is greater than the predetermined numerical value (15%) (S 54 ). When the absolute value of the handle operation data is greater than 15% (YES in S 54 ), the change factor determination unit 1205 determines that the factor of the change in the pulse wave amplitude is a change in the driver's fatigue level as shown in FIG. 36 , and outputs, to the fatigue evaluation unit 1109 , the current change amount from the starting point that is information to be used for evaluating the fatigue level (S 55 ).
  • the change factor determination unit 1205 determines that the factor of the change in the pulse wave amplitude is a change in the driver's thermal sensation as shown in FIG. 36 , and outputs, to the thermal sensation evaluation unit 108 , the current change amount from the starting point that is information to be used for evaluating the thermal sensation (S 56 ).
  • the device control device when a user's pulse wave changes, it is possible to determine the factor of the change in the pulse wave taking into account the time required for the change in addition to the change amount in the pulse wave. Further, with the device control device according to Embodiment 5, when a user's pulse wave changes, it is possible to determine the factor of the change in the pulse wave taking into account the handle operation data in addition to the change amount in the pulse wave. In other words, it is possible to discriminate the factor of the change in the pulse wave, that is, determine whether the change is due to a change in the thermal sensation or a change in the fatigue level. In addition, it is also possible to evaluate the user's thermal sensation or fatigue level based on the change factor.
  • the vital sign measurement unit 101 determines whether or not the pulse wave data includes noise based on the variance values of the component ratios. However, it is also good to determine whether or not the pulse wave data includes noise based on whether or not the component ratios fall within a predetermined range. For example, as shown in FIG. 9 , the ratio (component ratio) of the maximum value and the minimum value of the velocity plethysmogram changes significantly in Segments A and B affected by body movements, but changes slightly in Segment C affected by change in the thermal sensation. Accordingly, the component ratio in Segment C falls within the predetermined range.
  • FIG. 43 is a block diagram showing another structure of the vital signal measurement unit. It is assumed that the vital sign measurement unit 3101 is connected to the pulse wave sensor 1 .
  • the vital sign measurement unit 3101 includes a pulse wave detection unit 1011 , a pulse wave derivative unit 1012 , a component extraction unit 1013 , a component ratio calculation unit 1014 , a determination unit 3017 , a noise segment removal unit 1018 , and an accumulation unit 1019 .
  • the vital sign measurement unit 3101 does not include the component ratio storage unit 1015 and the variance value calculation unit 1016 , and includes a determination unit 1017 instead of the determination unit 3017 . For this reason, the same processing units as in the vital sign measurement unit 101 are not repeatedly described in detail here.
  • the determination unit 1017 determines whether or not the pulse wave includes noise based on the component ratio value calculated by the component ratio calculation unit 1014 .
  • FIG. 44 is a flowchart of processing performed by the vital sign measurement unit 3101 .
  • the same processing as indicated in the flowchart of the processing executed by the vital sign measurement unit 101 shown in FIG. 17 are assigned with the same step numbers, and no detailed descriptions are repeated here.
  • the vital sign measurement unit 3101 calculates the component ratios by executing the processes S 201 to S 205 .
  • the determination unit 3017 determines whether or not the calculated component ratios fall within the predetermined component ratio (for example, a range from ⁇ 0.1 to ⁇ 0.4) (S 306 ).
  • the determination unit 3017 determines that the detected pulse wave does not include noise, and the noise segment removal unit 1018 outputs the data indicating the pulse wave to the accumulation unit 1019 without performing noise removal (S 210 ).
  • the determination unit 3017 determines that the detected pulse wave includes noise, and the noise segment removal unit 1018 removes the pulse wave portion corresponding to the noise segment and outputs the data indicating the pulse wave which has been subjected to the noise removal to the accumulation unit 1019 (S 211 ).
  • the accumulation unit 1019 accumulates the pulse wave data outputted by the noise segment removal unit 1018 (S 212 ).
  • the vital sign measurement unit 101 checks whether or not a condition for terminating the current processing is satisfied (S 213 ). In the case where the termination condition is satisfied (YES in S 213 ), the vital sign measurement unit 101 terminates the processing. In the case where the termination condition is not satisfied (NO in S 213 ), the pulse wave detection unit 1011 continues the pulse wave detection process (S 201 ).
  • this variance makes it possible to discriminate a change in the pulse wave made by a change in the thermal sensation from noise caused due to the influence of body movements, by calculating the component ratios that are the ratios of the maximum values and the minimum values in predetermined time ranges of the velocity plethysmogram, and determining whether or not the component ratios fall within the predetermined component ratio range.
  • the threshold value for the change amount from the starting point and the previous change amount is 0.1
  • the threshold value for the change time from the change point is 10 minutes.
  • threshold values are not limited to those, and other predetermined numerical values may be used.
  • the threshold value for the change amount from the starting point and the previous change amount it is also good to use, instead of the predetermined numerical value, a numerical value (such as the value corresponding to 10% of the following average value) calculated based on the average value in a certain segment in the time-series data of the user's pulse wave amplitude.
  • the threshold value for the change amount from the starting point is 0.1 and the threshold value for the temperature change amount from the starting point is 3 degrees Celsius.
  • threshold values are not limited to these and other predetermined numerical values may be used.
  • the threshold value for the change amount from the starting point it is also good to use, instead of the predetermined numerical value, a numerical value (such as the value corresponding to 10% of the following average value) calculated based on the average value in a certain segment in the time-series data of the user's pulse wave amplitude.
  • the threshold value for the change amount from the starting point is 0.1 and the threshold value for the integration value of the change amounts each from the previous point is 1.
  • threshold values are not limited to these, and other predetermined numerical values may be used.
  • the threshold value for the change amount from the starting point it is also good to use, instead of the predetermined numerical value, a numerical value (such as the value corresponding to 10% of the following average value) calculated based on the average value in a certain segment in the time-series data of the user's pulse wave amplitude.
  • the threshold value for the change amount from the starting point is 0.1 and the threshold value for the handle operation data is 15%.
  • threshold values are not limited to these, and other predetermined numerical values may be used.
  • the threshold value for the change amount from the starting point it is also good to use, instead of the predetermined numerical value, a numerical value (such as the value corresponding to 10% of the following average value) calculated based on the average value in a certain segment in the time-series data of the user's pulse wave amplitude.
  • the parameter extraction unit 102 extracts the pulse wave amplitude as parameter values in the above-described Embodiments.
  • the parameter extraction unit 102 may extract, as parameter values, vital signs which are possibly used for evaluating a user's thermal sensation and health condition.
  • vital signs include: (i) the number of heartbeats and the number of pulses; (ii) waveform components (a, b, c, d, and e) of an accelerated plethysmogram obtained by performing second-order derivative on the pulse waveform and the waveform component ratios (b/a, c/a, d/a, and e/a); (iii) the ratio obtained using LF/HF and HF that are results of frequency analysis on the pulse wave intervals; and (iv) the Maximum Lyapunov exponents that are the result of chaotic analysis on the pulse waveform.
  • a, b, c, d, and e respectively denotes the amplitude values of Wave a, Wave b, Wave
  • the device control that is performed by either the device control unit 107 or the thermal sensation related device control unit 1114 may display the user's thermal sensation on a display device or output an alert according to the user's thermal sensation status.
  • the device control that is performed by either the device control unit 107 or the fatigue related device control unit 1113 may display the user's health condition or fatigue level on the display device or output an alert according to the user's health condition or fatigue level status.
  • the device control for making better the user's thermal sensation or the user's health condition may be the one that provides: thermal stimulation using warm or cool wind etc.; air flow stimulation using cool or warm wind etc.; physical stimulation using massage etc.; or physical stimulation using oxygen or negative ions etc.
  • control details determined in the case where it is evaluated that the thermal sensation is shifted to “hot” may include to lower the temperature in the thermal stimulation, and to increase air flow in the air flow stimulation.
  • control details determined in the case where it is evaluated that the thermal sensation is shifted to “cold” may include to raise the temperature in the thermal stimulation, and to decrease air flow in the air flow stimulation.
  • the current control details may be canceled.
  • the current control details may be continued.
  • the parameter extraction unit 102 extracts the pulse wave amplitude for each element wave of the pulse wave and outputs the pulse wave amplitude after each extraction.
  • the parameter extraction unit 102 may output the average value of the pulse wave amplitudes of the plural element waves of the pulse wave.
  • specific time points are predetermined for the starting time point in the time-series data of the pulse wave amplitude used by the parameter change amount calculation unit 103 , the parameter change time calculation unit 104 , and the parameter change amount integration unit 904 and the unit 505 for calculating a temperature change amount from a starting point.
  • the status evaluation unit 106 includes the thermal sensation evaluation unit 108 and the health condition evaluation unit 109 .
  • the health condition evaluation unit 109 classifies the evaluated health conditions in further detail, and includes a fatigue level evaluation unit, a stress evaluation unit, a sleepiness evaluation unit and the like.
  • the vital sign measurement units 101 and 1101 in the above-described Embodiments may use standard deviation values instead of the variance values of component ratios.
  • the vital sign measurement units 101 and 1101 in the above-described Embodiments determine whether or not the pulse wave includes noise based on the variance values. However, it is also good to provide each of the vital sign measurement unit with a storage device for storing the variance values and a processing unit for calculating the difference value of current two variance values, and determine mixture of noise depending on whether or not the difference value falls within a predetermined range.
  • the vital sign measurement unit 3101 in the above-described Variation determines whether or not the pulse wave includes noise based on the component ratio values.
  • each of the vital sign measurement unit with a storage device for storing the component ratio values and a processing unit for calculating the difference value of current two component ratio values, and determine mixture of noise depending on whether or not the difference value falls within a predetermined range.
  • the pulse wave sensor 1 is assumed to be a transparent optical sensor in the above-described Embodiments, but the pulse wave sensor 1 may be a reflection sensor or a piezoelectric sensor. In addition, it is also good that a pulse may be measured at the root of a finger or a palm.
  • the range (T 2 in FIG. 18 ) in which a minimum value is extracted by the component extraction unit 1013 is temporally backward of the point (M 1 in FIG. 18 ) at which a maximum values is extracted, but it is also good to extract the minimum value from the whole range (T 1 in FIG. 18 ).
  • each of the component ratios that is calculated by the component ratio calculation unit 1014 is the value obtained by dividing the minimum value by the maximum value, but it is also good that each of the component ratios that is calculated by the component ratio calculation unit 1014 is the value obtained by dividing the maximum value by the minimum value.
  • the pulse wave sensor 1 is provided on the handle of a vehicle in Embodiments 4 and 5, and measures a pulse wave of the driver while the driver is grasping the handle. This is not intended to limit the present invention. For example, it is also good to provide the pulse wave sensor 1 on a shift lever or an arm rest that is possibly touched by the driver or a rider, and causes the pulse wave sensor 1 to measure the pulse wave of the driver or the rider when touched.
  • a predetermined device is controlled according to the evaluation result by either the health condition evaluation unit 109 or the fatigue evaluation unit 1109 .
  • an implementation of simply recording health conditions and fatigue levels on a recorder is possible, and an implementation of transmitting health conditions and fatigue levels to a server via a network is also possible. It is also good to transmit these to the server only when the current fatigue level is greater than a predetermined threshold value.
  • the above Embodiments describe device control focusing on the applications to vehicles, but the device control may be used for other applications.
  • the device control may be used for other applications.
  • a system LSI is a single-chip super-multi-functional LSI configured to include plural structural means integrated thereon. More specifically, the super-multi-functional LSI is a computer system configured to include a microprocessor, a ROM, a RAM, and the like. The RAM stores a computer program. When the microprocessor operates according to the computer program, the system LSI implements the functions.
  • Embodiments disclosed above are exemplary in all respects, and thus are not intended to limit the present invention.
  • the scope of the present invention is defined by the CLAIMS not by the DESCRIPTION, and all possible modifications having equivalents to those in the CLAIMS and within the scope of the CLAIMS are intended to be included in the present invention.
  • the device control device can reliably evaluate a user status by discriminating the factor of a change in a vital sign that is a material for evaluating the user status when evaluating the user status based on the vital sign, and performs device control. Therefore, the device control device is useful as a device control device that controls an on-vehicle device based on the vital sign.

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Surgery (AREA)
  • Molecular Biology (AREA)
  • Physics & Mathematics (AREA)
  • Medical Informatics (AREA)
  • Biophysics (AREA)
  • Pathology (AREA)
  • Biomedical Technology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Psychiatry (AREA)
  • Physiology (AREA)
  • Cardiology (AREA)
  • Signal Processing (AREA)
  • Vascular Medicine (AREA)
  • Child & Adolescent Psychology (AREA)
  • Hospice & Palliative Care (AREA)
  • Artificial Intelligence (AREA)
  • Psychology (AREA)
  • Developmental Disabilities (AREA)
  • Social Psychology (AREA)
  • Computer Vision & Pattern Recognition (AREA)
  • Educational Technology (AREA)
  • Measuring Pulse, Heart Rate, Blood Pressure Or Blood Flow (AREA)
  • Measurement Of The Respiration, Hearing Ability, Form, And Blood Characteristics Of Living Organisms (AREA)
  • Measuring And Recording Apparatus For Diagnosis (AREA)
  • Steering Controls (AREA)
  • Air-Conditioning For Vehicles (AREA)
  • Navigation (AREA)
  • User Interface Of Digital Computer (AREA)
  • Radar Systems Or Details Thereof (AREA)
US12/663,342 2007-06-08 2008-06-06 Device control device and device control method Abandoned US20100179441A1 (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
JP2007152309 2007-06-08
JP2007-152308 2007-06-08
JP2007-152309 2007-06-08
JP2007152308 2007-06-08
PCT/JP2008/001447 WO2008149558A1 (fr) 2007-06-08 2008-06-06 Dispositif de contrôle d'appareil et procédé de contrôle d'appareil

Publications (1)

Publication Number Publication Date
US20100179441A1 true US20100179441A1 (en) 2010-07-15

Family

ID=40093390

Family Applications (2)

Application Number Title Priority Date Filing Date
US12/663,342 Abandoned US20100179441A1 (en) 2007-06-08 2008-06-06 Device control device and device control method
US12/663,388 Expired - Fee Related US8425427B2 (en) 2007-06-08 2008-06-06 Pulse wave detection device, device control device, and pulse wave detection method

Family Applications After (1)

Application Number Title Priority Date Filing Date
US12/663,388 Expired - Fee Related US8425427B2 (en) 2007-06-08 2008-06-06 Pulse wave detection device, device control device, and pulse wave detection method

Country Status (5)

Country Link
US (2) US20100179441A1 (fr)
EP (2) EP2151189B1 (fr)
JP (2) JP4964953B2 (fr)
CN (2) CN101677773B (fr)
WO (2) WO2008149559A1 (fr)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20120136218A1 (en) * 2010-11-26 2012-05-31 Samsung Electronics Co., Ltd Remote healthcare system and healthcare method using the same
US8706206B2 (en) 2009-10-29 2014-04-22 Panasonic Corporation Human fatigue assessment device and human fatigue assessment method
CN107908819A (zh) * 2017-10-19 2018-04-13 深圳和而泰智能控制股份有限公司 预测用户状态变化的方法和装置
US20190269361A1 (en) * 2016-10-21 2019-09-05 Citizen Watch Co., Ltd. Detection device
US11540779B2 (en) 2017-12-29 2023-01-03 Samsung Electronics Co., Ltd. Bio-information measuring apparatus and bio-information measuring method

Families Citing this family (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5098721B2 (ja) * 2008-03-14 2012-12-12 オムロンヘルスケア株式会社 血圧測定装置、血圧導出プログラムおよび血圧導出方法
JP5516428B2 (ja) * 2010-10-14 2014-06-11 株式会社村田製作所 拍動周期算出装置およびこれを備えた生体センサ
CN103619243B (zh) * 2011-06-24 2016-05-04 株式会社村田制作所 移动设备
JP5998516B2 (ja) * 2012-02-23 2016-09-28 セイコーエプソン株式会社 拍動検出装置、電子機器及びプログラム
CN102645002A (zh) * 2012-04-16 2012-08-22 广东美的制冷设备有限公司 一种生物信号的空调器控制系统及其控制方法
JP5839698B2 (ja) * 2012-05-07 2016-01-06 日本電信電話株式会社 生体情報加工装置及びプログラム
CN102881117B (zh) * 2012-06-15 2014-11-12 浙江吉利汽车研究院有限公司杭州分公司 一种带有驾驶员疲劳检测的手表
KR101614735B1 (ko) * 2014-12-08 2016-04-22 현대자동차주식회사 Avn 단말, 이를 포함하는 차량, 및 차량의 제어방법
CN104490374A (zh) * 2014-12-09 2015-04-08 财团法人车辆研究测试中心 驾驶者心脏状态的判断系统及方法
CN106264449B (zh) * 2015-06-29 2022-01-28 松下知识产权经营株式会社 人状态推定方法和人状态推定系统
JP6739038B2 (ja) * 2015-06-29 2020-08-12 パナソニックIpマネジメント株式会社 人状態推定方法、及び、人状態推定システム
JP6582788B2 (ja) 2015-09-17 2019-10-02 富士通株式会社 眠気検知装置、眠気検知方法および眠気検知プログラム
CN106562793B (zh) * 2015-10-08 2021-12-21 松下电器(美国)知识产权公司 信息提示装置的控制方法、以及信息提示装置
JP6985005B2 (ja) * 2015-10-14 2021-12-22 パナソニック インテレクチュアル プロパティ コーポレーション オブ アメリカPanasonic Intellectual Property Corporation of America 感情推定方法、感情推定装置、及び、プログラムを記録した記録媒体
CN105962910A (zh) * 2016-06-08 2016-09-28 深圳市中识创新科技有限公司 脉象采集方法及装置
JP6945127B2 (ja) * 2016-09-16 2021-10-06 パナソニックIpマネジメント株式会社 ストレスマネジメントシステム、ストレスマネジメント方法及びコンピュータプログラム
WO2018100755A1 (fr) * 2016-11-30 2018-06-07 京セラ株式会社 Dispositif de mesure d'informations biologiques, procédé de mesure d'informations biologiques et système de support de mesure d'informations biologiques
JP6228326B1 (ja) * 2017-01-25 2017-11-08 京セラ株式会社 携帯端末装置、生体情報測定方法、及び生体情報測定システム
JP2018089000A (ja) * 2016-11-30 2018-06-14 京セラ株式会社 生体情報測定装置、生体情報測定方法、及び生体情報測定システム
EP3403572A1 (fr) 2017-05-17 2018-11-21 My-Vitality SàRL Dispositif de diagnostic d'onde d'impulsion et procédé de calcul et de détermination de fatigue
WO2019014931A1 (fr) * 2017-07-21 2019-01-24 深圳市汇顶科技股份有限公司 Procédé et appareil d'analyse des interférences pour signal biologique, et dispositif portable
CN108045202B (zh) * 2017-12-27 2023-09-19 浙江梵力得健康科技有限公司 汽车遮阳板式空气净化器
JP6985180B2 (ja) * 2018-02-27 2021-12-22 ファナック株式会社 数値制御装置
US20210030358A1 (en) * 2018-03-09 2021-02-04 Mitsubishi Electric Corporation State of discomfort determination device
CN109009003B (zh) * 2018-07-09 2021-06-25 东南大学 一种脉搏信号检测的控制方法
CN111529829B (zh) * 2020-07-07 2020-11-27 深圳市汇顶科技股份有限公司 一种ppg设备的信号调整方法和ppg设备
WO2022006747A1 (fr) 2020-07-07 2022-01-13 深圳市汇顶科技股份有限公司 Procédé de réglage de signal d'appareil ppg et appareil ppg
JP7582132B2 (ja) * 2021-09-03 2024-11-13 株式会社島津製作所 ワイヤロープ検査方法、ワイヤロープ検査システム、および、ワイヤロープ検査装置
KR102445826B1 (ko) * 2021-12-01 2022-09-22 주식회사 에스비솔루션 헬스케어 기능이 내장된 차량용 핸들장치 및 핸들장치의 생체 정보 측정 방법
CN120531395B (zh) * 2025-05-28 2026-01-02 青岛理工大学 一种基于后颈皮肤温度的精神疲劳实时监测方法及系统

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6496723B1 (en) * 1999-08-30 2002-12-17 Denso Corporation Method of obtaining information that corresponds to electrocardiogram of human body from pulse wave thereof
US20060247542A1 (en) * 2003-06-27 2006-11-02 Yasuyoshi Watanabe Fatigue degree estimating method, fatigue degree estimating device, and database
US20060281995A1 (en) * 2001-07-09 2006-12-14 Hiroyuki Muramatsu Blood rheology measuring apparatus
US20090124926A1 (en) * 2005-12-05 2009-05-14 Masami Funakura Environment control device, environment control method, environment control program, and environment control system
US20090276062A1 (en) * 2005-07-11 2009-11-05 Etsuko Kanai Environment control device, environment control method, environment control program, and computer-readable recording medium containing the environment control program

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5368026A (en) * 1993-03-26 1994-11-29 Nellcor Incorporated Oximeter with motion detection for alarm modification
JP3596158B2 (ja) * 1996-05-21 2004-12-02 松下電器産業株式会社 運転者モニター装置とこれを用いた安全装置
JP3250474B2 (ja) 1996-11-07 2002-01-28 日産自動車株式会社 メンタルストレス判定装置
JP3596198B2 (ja) * 1996-11-20 2004-12-02 松下電器産業株式会社 運転者監視装置
JPH11151230A (ja) * 1997-11-19 1999-06-08 Nissan Motor Co Ltd 車両用運転者状態計測装置
JPH11151231A (ja) * 1997-11-20 1999-06-08 Nissan Motor Co Ltd 車両用精神疲労度判定装置
EP1107691A4 (fr) * 1998-08-24 2005-04-06 Martin C Baruch Appareil et procede permettant de mesurer le temps de transit d'impulsion
JP3835073B2 (ja) 1999-08-30 2006-10-18 株式会社デンソー 脈波計測装置
JP2001204714A (ja) 2000-01-28 2001-07-31 Nissan Motor Co Ltd メンタルストレス判定装置
JP2003061921A (ja) 2001-08-30 2003-03-04 Mitsuba Corp 体調判別方法および体調判別装置
JP3923035B2 (ja) 2003-07-03 2007-05-30 株式会社東芝 生体状態分析装置及び生体状態分析方法
JP2007097615A (ja) 2005-09-30 2007-04-19 Matsushita Electric Works Ltd 循環器機能測定システム
JP2007117591A (ja) * 2005-10-31 2007-05-17 Konica Minolta Sensing Inc 脈波解析装置
DE102006051561A1 (de) * 2005-11-15 2007-05-24 Weinmann Geräte für Medizin GmbH + Co. KG Anzeigemittel für Vitalparameter

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6496723B1 (en) * 1999-08-30 2002-12-17 Denso Corporation Method of obtaining information that corresponds to electrocardiogram of human body from pulse wave thereof
US20060281995A1 (en) * 2001-07-09 2006-12-14 Hiroyuki Muramatsu Blood rheology measuring apparatus
US20060247542A1 (en) * 2003-06-27 2006-11-02 Yasuyoshi Watanabe Fatigue degree estimating method, fatigue degree estimating device, and database
US20090276062A1 (en) * 2005-07-11 2009-11-05 Etsuko Kanai Environment control device, environment control method, environment control program, and computer-readable recording medium containing the environment control program
US20090124926A1 (en) * 2005-12-05 2009-05-14 Masami Funakura Environment control device, environment control method, environment control program, and environment control system

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
English machine translation from JPO of WO2007/007632 *
English machine translation from WIPO patent scope of WO2007/007632 *
English Translation of JP 11-151230 *

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8706206B2 (en) 2009-10-29 2014-04-22 Panasonic Corporation Human fatigue assessment device and human fatigue assessment method
US20120136218A1 (en) * 2010-11-26 2012-05-31 Samsung Electronics Co., Ltd Remote healthcare system and healthcare method using the same
US20190269361A1 (en) * 2016-10-21 2019-09-05 Citizen Watch Co., Ltd. Detection device
US11793448B2 (en) * 2016-10-21 2023-10-24 Citizen Watch Co., Ltd. Detection device
CN107908819A (zh) * 2017-10-19 2018-04-13 深圳和而泰智能控制股份有限公司 预测用户状态变化的方法和装置
US11540779B2 (en) 2017-12-29 2023-01-03 Samsung Electronics Co., Ltd. Bio-information measuring apparatus and bio-information measuring method

Also Published As

Publication number Publication date
US8425427B2 (en) 2013-04-23
CN101677773A (zh) 2010-03-24
JP4964953B2 (ja) 2012-07-04
JPWO2008149559A1 (ja) 2010-08-19
CN101677772A (zh) 2010-03-24
EP2156788A1 (fr) 2010-02-24
EP2151189A1 (fr) 2010-02-10
US20100217137A1 (en) 2010-08-26
EP2151189A4 (fr) 2014-01-22
EP2151189B1 (fr) 2015-11-04
CN101677773B (zh) 2011-11-02
JPWO2008149558A1 (ja) 2010-08-19
WO2008149559A1 (fr) 2008-12-11
CN101677772B (zh) 2011-12-28
WO2008149558A1 (fr) 2008-12-11

Similar Documents

Publication Publication Date Title
US8425427B2 (en) Pulse wave detection device, device control device, and pulse wave detection method
CN112109615B (zh) 座椅系统和控制方法
US7397382B2 (en) Drowsiness detecting apparatus and method
JP4111062B2 (ja) 眠気度合検出装置
JP4505619B2 (ja) 心身状態判定システム
EP2285265B1 (fr) Procédé et dispositif pour la détection d'évènements de micro-sommeil
JP5155805B2 (ja) 睡眠制御装置
US9050045B2 (en) Psychological state estimation device
JP2007203913A (ja) 運転支援装置及び運転支援システム
JP4802842B2 (ja) 健康管理支援装置及び健康管理システム
JP4701694B2 (ja) 覚醒度判定装置及び覚醒度判定方法
US20040236235A1 (en) Human condition evaluation system, computer program, and computer-readable record medium
JP3596198B2 (ja) 運転者監視装置
KR100634549B1 (ko) 건강관리장치 및 방법
JP4867215B2 (ja) 生理・心理状態判定装置、生理・心理状態判定方法、リファレンスデータ生成装置、及びリファレンスデータ生成方法。
CN107007292B (zh) 用于获知疲劳的方法
JP2002291710A (ja) 睡眠解析装置及びプログラム並びに記録媒体
JP2007000280A (ja) 覚醒度低下判定装置
JP2010012100A (ja) 眠気検出装置
Razak et al. Driver-centered pervasive application for heart rate measurement
JPH09154835A (ja) 居眠り検出装置
JP2007044154A (ja) 覚醒度判定方法
JPH08196636A (ja) 居眠り警告装置
JP4797646B2 (ja) 覚醒度推定装置および覚醒度推定方法
JP2006298234A (ja) 覚醒度判定装置および方法

Legal Events

Date Code Title Description
AS Assignment

Owner name: PANASONIC CORPORATION, JAPAN

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:KANAI, ETSUKO;FUNAKURA, MASAMI;MAEDA, YASUTAKA;AND OTHERS;SIGNING DATES FROM 20091030 TO 20091105;REEL/FRAME:023847/0288

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION