WO2024039450A1 - Techniques de détermination et de gestion de score de fatigue de condition physique - Google Patents

Techniques de détermination et de gestion de score de fatigue de condition physique Download PDF

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Publication number
WO2024039450A1
WO2024039450A1 PCT/US2023/026837 US2023026837W WO2024039450A1 WO 2024039450 A1 WO2024039450 A1 WO 2024039450A1 US 2023026837 W US2023026837 W US 2023026837W WO 2024039450 A1 WO2024039450 A1 WO 2024039450A1
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Prior art keywords
user
data
period
time
fitness
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PCT/US2023/026837
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English (en)
Inventor
Stuart Blanché TRUAX
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Fitbit Llc
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Priority claimed from US17/891,428 external-priority patent/US20220406453A1/en
Application filed by Fitbit Llc filed Critical Fitbit Llc
Publication of WO2024039450A1 publication Critical patent/WO2024039450A1/fr

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    • G—PHYSICS
    • G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
    • G16H50/00—ICT specially adapted for medical diagnosis, medical simulation or medical data mining; ICT specially adapted for detecting, monitoring or modelling epidemics or pandemics
    • G16H50/30—ICT specially adapted for medical diagnosis, medical simulation or medical data mining; ICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for calculating health indices; for individual health risk assessment
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/02—Detecting, measuring or recording pulse, heart rate, blood pressure or blood flow; Combined pulse/heart-rate/blood pressure determination; Evaluating a cardiovascular condition not otherwise provided for, e.g. using combinations of techniques provided for in this group with electrocardiography or electroauscultation; Heart catheters for measuring blood pressure
    • A61B5/024—Detecting, measuring or recording pulse rate or heart rate
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/05—Detecting, measuring or recording for diagnosis by means of electric currents or magnetic fields; Measuring using microwaves or radio waves 
    • A61B5/053—Measuring electrical impedance or conductance of a portion of the body
    • A61B5/0531—Measuring skin impedance
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/16—Devices for psychotechnics; Testing reaction times ; Devices for evaluating the psychological state
    • A61B5/165—Evaluating the state of mind, e.g. depression, anxiety
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/48—Other medical applications
    • A61B5/4806—Sleep evaluation
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/68—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient
    • A61B5/6801—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient specially adapted to be attached to or worn on the body surface
    • A61B5/6802—Sensor mounted on worn items
    • A61B5/681—Wristwatch-type devices
    • G—PHYSICS
    • G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
    • G16H40/00—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices
    • G16H40/60—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices
    • G16H40/63—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices for local operation
    • G—PHYSICS
    • G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
    • G16H40/00—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices
    • G16H40/60—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices
    • G16H40/67—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices for remote operation
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/05—Detecting, measuring or recording for diagnosis by means of electric currents or magnetic fields; Measuring using microwaves or radio waves 
    • A61B5/053—Measuring electrical impedance or conductance of a portion of the body
    • A61B5/0531—Measuring skin impedance
    • A61B5/0533—Measuring galvanic skin response
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/103—Detecting, measuring or recording devices for testing the shape, pattern, colour, size or movement of the body or parts thereof, for diagnostic purposes
    • A61B5/11—Measuring movement of the entire body or parts thereof, e.g. head or hand tremor, mobility of a limb
    • A61B5/1118—Determining activity level
    • G—PHYSICS
    • G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
    • G16H20/00—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance
    • G16H20/30—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to physical therapies or activities, e.g. physiotherapy, acupressure or exercising
    • G—PHYSICS
    • G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
    • G16H20/00—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance
    • G16H20/70—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to mental therapies, e.g. psychological therapy or autogenous training
    • G—PHYSICS
    • G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
    • G16H50/00—ICT specially adapted for medical diagnosis, medical simulation or medical data mining; ICT specially adapted for detecting, monitoring or modelling epidemics or pandemics
    • G16H50/20—ICT specially adapted for medical diagnosis, medical simulation or medical data mining; ICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for computer-aided diagnosis, e.g. based on medical expert systems
    • G—PHYSICS
    • G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
    • G16H50/00—ICT specially adapted for medical diagnosis, medical simulation or medical data mining; ICT specially adapted for detecting, monitoring or modelling epidemics or pandemics
    • G16H50/70—ICT specially adapted for medical diagnosis, medical simulation or medical data mining; ICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for mining of medical data, e.g. analysing previous cases of other patients

Definitions

  • the present disclosure is directed to a technical solution/benefit to the aforementioned technical problem. Accordingly, the present disclosure is directed to a system and method for calculating a stress score for a user of a wearable device.
  • the stress score can be calculated using electro-dermal activity (EDA) data collected from an EDA sensor while the user is wearing the wearable device.
  • EDA electro-dermal activity
  • the sympathetic nervous system can trigger micro-perspiration throughout a person’s body, so conductance between the EDA sensor on the wearable device and a hand or fingertip of the user will increase as the perspiration levels increase.
  • the EDA sensor can generate data that can be used by the wearable device to accurately and automatically calculate stress of the user.
  • a method for determining a fitness fatigue score for a user includes obtaining first data for the user over a first period of time.
  • the first data includes a plurality of heart rate measurements for the user over the first period of time.
  • the method includes obtaining second data for the user over a second portion of time that is shorter in duration than the first period of time.
  • the second data includes one or more sleep metrics for a plurality of sleep events for the user over the second period of time.
  • the method includes obtaining third data for the user over a third period of time that is longer in duration than the first period of time.
  • the third data includes heart rate variability data for the user over the third period of time.
  • the method includes determining the fitness fatigue score for the user for a current day based, at least in part, on the first data, the second data, and the third data.
  • the method includes causing a display screen of an electronic device to display the fitness fatigue score.
  • the one or more sleep metrics can include a duration of each of the plurality of sleep events.
  • the one or more sleep metrics can include a time of day at which each of the sleep events occurred.
  • the first period of time can include 14 days immediately prior to the cunent day.
  • the second period of time can include 7 days immediately prior to the current day.
  • the third period of time can include 30 days immediately prior to the current day.
  • the method includes determining a recommendation regarding exercise for the current day based, at least in part, on the determined fitness fatigue score for the current day.
  • the method includes causing the display screen of the electronic device to display the recommendation regarding exercise.
  • the recommendation can be for the user to forego exercise on the current day when the fitness fatigue score for the current day is below a first threshold value.
  • the recommendation can be for the user to engage in a first physical activity on the current day when the fitness fatigue score for the current day is greater than the first threshold value and less than a second threshold value.
  • the recommendation can be for the user to engage in a second physical activity on the current day when the fitness fatigue score for the current day is greater than the second threshold value.
  • the second physical activity can be more strenuous than the first physical activity.
  • determining the fitness fatigue score for the user for the current day includes determining a first subscore based on the first data. Determining the fitness fatigue score for the user further includes determining a second subscore based on the second data and a third subscore for the user based, at least in part, on the third data. Furthermore, determining the fitness fatigue score includes determining the fitness fatigue score for the user for the current day based, at least in part, on the first subscore, the second subscore, and the third subscore. In some embodiments, the first subscore is weighted more heavily than each of the second subscore and the third subscore.
  • determining the fitness fatigue score includes determining the first subscore is less than a threshold value and determining the fitness fatigue score for the current day is the first subscore.
  • determining the first subscore based on the first data includes determining a reserve value for each of the plurality of heart rate measurements included in the first data. Determining the first subscore further includes determining the reserve value for one or more of the heart rate measurements is greater than a threshold value. Determining the first subscore even further includes determining the first subscore based, at least in part, on the one or more heart rate measurements whose reserve value is greater than the threshold value.
  • detennining the reserve value for each of the heart rate measurements includes determining a resting heart rate of the user based, at least in part, on the first data and determining a maximum heart rate of the user based, at least in part, on an age of the user. Determining the reserve value further includes determining the reserve value for each of the plurality of heart rate measurements based, at least in part, on a comparison of each of the respective heart rate measurements to the resting heart rate of the user and the maximum heart rate of the user.
  • the heart rate variability data includes heart rate variability measurements taken during each of a plurality of sleep events occurring over the third period of time. Furthermore, determining the third subscore based, at least in part, on the heart rate variability data includes determining a root mean square of successive differences of heart rate variability measurements associated with a first sleep event of the plurality of sleep events. The first sleep event can corresponding to the most recent in time sleep event of the plurality of sleep events. The method includes determining the third subscore based, at least in part, on a comparison of the heart rate variability measurements associated with the first sleep event to the heart rate variability measurements for at least one other sleep event of the plurality of sleep events.
  • FIGS. 1A and IB illustrate an example device that can be used to obtain and analyze user health information in accordance with various embodiments.
  • FIG. 2 illustrates an example set of devices that are able to communicate in accordance with various embodiments.
  • FIG. 3 illustrates an example stress score algorithm that can be utilized in accordance with various embodiments.
  • FIG. 4 illustrates example interfaces that can be provided in accordance with various embodiments.
  • FIG. 5 illustrates example interfaces that can be provided in accordance with various embodiments.
  • FIG. 6 illustrates example interfaces that can be provided in accordance with various embodiments.
  • FIG. 7 illustrates an example process for determining a stress score that can be utilized in accordance with various embodiments.
  • FIG. 8 illustrates an example process for monitoring stress for a user that can be utilized in accordance with various embodiments.
  • FIG. 9 illustrates an example environment in which aspects of various embodiments can be implemented.
  • FIG. 10 illustrates a flow diagram of a method for determining a fitness fatigue score according to some embodiments of the present disclosure.
  • FIG. 11 depicts a flow diagram of a method for determining a first subscore of a fitness fatigue score according to some embodiments of the present disclosure.
  • FIG. 12 depicts a flow diagram of a method for determining a third subscore of a fitness fatigue score according to some embodiments of the present disclosure.
  • FIG. 13 depicts a graphical user interface displaying a fitness fatigue score on a display screen of an electronic device according to some embodiments of the present disclosure.
  • FIG. 14 depicts a graphical user interface displaying a fitness fatigue score on a display screen of a wearable computing device according to some embodiments of the present disclosure.
  • FIG. 15 depicts a graphical user interface for a fitness fatigue score on a display screen of a mobile computing device according to some embodiments of the present disclosure.
  • FIG. 16 depicts a graphical user interface displaying exercise recommendations for a user according to a fitness fatigue score for the user according to some embodiments of the present disclosure.
  • FIG. 17 depicts a graphical user interface displaying fitness fatigue scores for a user over a period of time according to some embodiments of the present disclosure.
  • Computing devices may include one or more sensors to detect physiological information about the user and/or the environment around the user. This information can be used to observe, detect, or diagnose various health conditions outside of a traditional clinic or laboratory setting. For example, in the context of monitoring stress, portable or wearable electronic devices may be able to detect when the sympathetic nervous system of the user triggers micro-perspiration throughout the user’s body. Additionally, a computing device may be able to record and interpret the detected information about the user and/or environment, to determine a health assessment.
  • a wearable electronic device may be able to record a relatively high frequency of a skin conductance response (SCR), which looks at the number of spikes in the skin conductance within a sliding window of time, and generate an assessment that the user is experiencing stress.
  • SCR skin conductance response
  • Approaches in accordance with various embodiments provide for determination, prediction, and/or monitoring of factors that can be indicative of stress or other such states of a user. In at least one embodiment, this determination can be made based, at least in part, upon data collected by a wearable computer, such as a device 100 illustrated in the embodiment of FIG. 1A.
  • a person can wear or utilize the device 100 that is able to automatically measure or determine at least some aspects of the health or wellbeing of the person.
  • the device 100 is a smart watch 104, although other devices such as smart or connected fitness bands or trackers, watches, rings, earbuds, phones, clothing, and the like can be utilized as well within the scope of the various embodiments.
  • the person can wear the device 100 on an arm 102 or wrist, and can view content, as may include health information, on a display 106 of the device.
  • the display 106 is a touch sensitive display that allows the person to input or annotate information about that person’s health or status as discussed elsewhere herein.
  • the device 100 may include various measurement components 152, 154 (also referred to herein as sensors) as illustrated in the back view 150 of the device 100. More specifically, as shown, the device 100 may include one or more internal sensors 152 and/or one or more external sensors 154, which may include any suitable type of sensors, such as EDA sensors and/or motion and temperature sensors, that can be used to measure or detect information about the user. Further, in an embodiment, the measurement components 152, 154 can include, or relate to, an optical measurement subsystem. In this example, the optical measurement sub-system includes at least one optical emitter and at least one optical receiver.
  • the emitter can emit light of one or more wavelengths that can be reflected from the surface of the wearer’s skin, or diffusely reflected after traveling, under the surface, and detected by at least one of the emitters.
  • Such an optical assembly can enable the smart watch to measure various types of information during times in which a person is wearing the device.
  • the external sensor(s) 154 may include an EDA sensor that is easily accessible by a palm or finger of the user, such that the user can easily make contact with the EDA sensor so that the sensor can generate data that can be used by the device 100 to accurately and automatically calculate stress of the user. Accordingly, the present disclosure is tied to the practical application of accurately and automatically calculating stress of the user through the EDA sensor(s) 154.
  • FIG. 2 illustrates an example environment 200 in which aspects of various embodiments can be implemented.
  • a person might have a number of different devices that are able to communicate using at least one wireless communication protocol.
  • the user might have a smart watch 202 or fitness tracker, which the user would like to be able to communicate with a smart phone 204 and a tablet computer 206.
  • the ability to communicate with multiple devices can enable a user to obtain information from the smart watch 202, such as heart rate data captured using a sensor on the smart watch, using an application installed on either the smart phone 204 or the tablet computer 206.
  • the user may also want the smart watch 202 to be able to communicate with a service provider 208, or other such entity, that is able to obtain and process data from the smartwatch and provide functionality that may not otherwise be available on the smartwatch or the applications installed on the individual devices.
  • the smart watch 202 may be able to communicate with the service provider 208 through at least one network 210, such as the Internet or a cellular network, or may communicate over a wireless connection such as Bluetooth® to one of the individual devices, which can then communicate over the at least one network.
  • a wireless connection such as Bluetooth®
  • a user may also want the devices to be able to communicate in a number of ways or with certain aspects.
  • the user may want communications between the devices to be secure, particularly where the data may include personal health data or other such communications.
  • the device or application providers may also be required to secure this information in at least some situations.
  • the user may want the devices to be able to communicate with each other concurrently, rather than sequentially. This may be particularly true where pairing may be required, as the user may prefer that each device be paired at most once, or that not manual pairing is required.
  • the user may also desire the communications to be as standards-based as possible, not only so that little manual intervention is required on the part of the user but also so that the devices can communicate with as many other types of devices as possible, which is often not the case for various proprietary formats.
  • a user may thus desire to be able to walk in a room with one device and have such device automatically communicate with another target device with little to no effort on the part of the user.
  • a device will utilize a communication technology such as Wi-Fi to communicate with other devices using wireless local area networking (WLAN).
  • WLAN wireless local area networking
  • Smaller or lower capacity devices, such as many Internet of Things (loT) devices instead utilize a communication technology such as Bluetooth®, and in particular Bluetooth Low Energy (BLE) that has very low power consumption.
  • the environment 200 illustrated in FIG. 2 enables data to be captured, processed, and displayed in a number of different ways.
  • data may be captured using sensors on a smart watch 202, but due to limited resources on that smart watch the data may be transferred to a smart phone 204 or the service provider 208 (or a cloud resource) for processing, and results of that processing may then be presented back to that user on the smart watch 202, smart phone 204, or another such device associated with that user, such as the tablet computer 206.
  • a user may also be able to provide input such as health data using an interface on any of these devices, which can then be considered when making that determination.
  • data determined for a user can be used to determine state information, such as may relate to a current stress level or state of that user. At least some of this data can be determined using sensors or components able to measure or detect aspects of a user, while other data may be manually input by that user or otherwise obtained.
  • a stress determination algorithm can be utilized that takes as input a number of different inputs, where different inputs can be obtained manually, automatically, or otherwise.
  • such an algorithm can take various types of factors and use these to generate a stress score.
  • One such stress score can be calculated as illustrated in approach 300 of FIG. 3. In this example, the stress score is calculated as a weighted sum of different types of factors.
  • these types of factors can include sleep features (e.g., restlessness, fragmentation), activity features (e.g., relative AZMs, relative steps), and/or heart features (e.g., HF/LF HRV, elevated heart rate at rest), as well as inputs such as electro-dermal activity (EDA), where EDA can be used to measure a galvanic skin response.
  • sleep features e.g., restlessness, fragmentation
  • activity features e.g., relative AZMs, relative steps
  • heart features e.g., HF/LF HRV, elevated heart rate at rest
  • EDA electro-dermal activity
  • these factors can be normalized, and then weights determined through testing, machine learning, or other such approaches.
  • a first feature type relating to sleep features, can include features such as the following.
  • a sleep score restlessness value can provide a measure of an amount of movement during sleep, which may be normalized for a person over a period such as 30 days. Restless sleep is a known physiological stress marker.
  • a fragmentation feature can indicate the number of times a person was awake for more than a threshold amount of time, such as 30 minutes (WASO), which may be normalized as an average over a period such as 30 days. Fragmented sleep is also known to be a physiological stress marker.
  • WASO 30 minutes
  • a sleep reservoir level indicates how well a person has slept over, for example, a last week with days further away affecting the score less, normalized over population level. This metric analyzes the user’s sleep from the last week, to account for the fact that multiple bad nights of sleep cannot always be recovered from in a single night of sleep. Overall sleep duration also can cause poor emotion regulation, and so situations that may not induce stress after a good night’s sleep can become stressful.
  • a set of constants can be determined and/or utilized to calculate a rate at which a user’s sleep reservoir level depletes.
  • a sleep reservoir level can represent an accumulated amount of restful sleep that a user has had over a recent period of time, such as a last seven days of sleeping.
  • this reservoir level will deplete, getting closer to zero but at different rates. If the user is very well rested, getting at least seven hours of sleep each of the past seven days, then this value may be closer to a maximum normalized value of one (1 ).
  • Such an approach can map sleep calculations into a normalized sleep reservoir scale, using specific constants that can determine a rate at which a user depletes his or her sleep, and how a particular sleeping period may accumulate in terms of sleep.
  • a first period of sleep is not counted as restful sleep, with only sleep beyond that initial period being determined to count as restful sleep. After this initial period the user can be determined to be accumulating sleep. A state or type of sleep after that initial period can then determine an amount or rate of restfulness that is being restored.
  • a deep and/or REM sleep duration can indicate, for example, minutes of deep sleep and percentage of REM (rapid eye movement) sleep for a most recent night, normalized using demographic group average over a period such as the last 30 days.
  • a deep sleep latency feature can indicate a number of minutes before first entering deep sleep after falling asleep, which can be normalized using a personal average over, for example, the last 30 days. Longer latency between the start of sleep and the first deep sleep period is known to be a physiological stress marker.
  • Feature value can increase when AZMs are higher or lower than a range around 150.
  • these minutes can be determined using sensors, such as motion and heart rate sensors, on a device. Too little weekly activity can result in increased cortisol levels and make one more susceptible to perceiving events as stressors, since mild to moderate exercise acts as a “shield” against stress. Too much weekly activity can result in fatigue, as exercise is by definition a stressor.
  • a stressor represents a stimulus or event that cases a state of strain or tension, and thus results in a stress response.
  • a stress response represents the physiological and psychological changes that a body undergoes in response to a stressor in an attempt to maintain homeostasis. Multiple stress responses can be elicited by a single stressor.
  • a psychological stress response represents a relationship between a person and the environment that is appraised by the person as taxing or exceeding his or her resources and endangering his or her well-being.
  • Another feature can be a step count value, corresponding to a total number of steps over a period, such as per day. This can be normalized using demographic group average over a period such as 30 days. Too few daily steps can result in increased cortisol levels and make one more susceptible to perceiving events as stressors, since mild to moderate exercise acts as a “shield” against stress. Too many daily steps can result in fatigue, as exercise is by definition a stressor. There can be other factors indicative of activity as well, where different types of data are analyzed to determine different types, or amounts, of activity.
  • Heart rate variability quantifies the variability in time between heart-beats.
  • LF Low Frequency
  • HF High Frequency
  • Elevated heart rate while resting during the day is a sign of increased sympathovagal balance, which means too much sympathetic nervous system (SNS) activity and not enough parasympathetic nervous system (PNS) activity. While stress results in an increased sympathovagal balance, many other things can cause increased heart rate including anemia, caffeine, alcohol, fever, high or low blood pressure, electrolyte imbalance (possibly from dehydration), hyperthyroidism, smoking, or medications.
  • SNS sympathetic nervous system
  • PNS parasympathetic nervous system
  • a sleeping heart rate above resting heart rate can indicate a percentage of time during sleep that the user’s HR is above resting HR, as may be normalized using an absolute metric as a raw percentage. Similar to Elevated HR at Rest, this is also a measure of sympatho-vagal balance, but quantifies HR during sleep instead of during the day. While many factors can cause this metric to be high, specifically drinking alcohol before sleep drives this to be high.
  • a fitness fatigue score can be calculated, which balances the fatigue effects of exercise with fitness effects of exercise into a single score, as may be normalized using a personal min/max range over a period such as 30-90 days.
  • This score measures the dual contributions of exercise to one’s fitness level in the long term, and fatigue in the short term, as measured through heart rate. Similar to weekly activity and daily steps, high fatigue levels are by definition stress that require rest.
  • Fitness fatigue can treat the human heart as a linear system. By measuring heart rate over a period of time, an accumulated representation of an amount of fatigue on a human body can be obtained, as quantified by a fitness fatigue score. When a user goes through a high heart rate event like an exercise, there will be a time when this score will go down, reflecting the fatigue effects of this exercise. After that period there will be a period where the score will go up, to reflect the fact that the body has become more fit and more resilient to exercise, and is better prepared for exercise events in the future.
  • EDA data can also be considered as a stress determination factor as discussed above.
  • Approaches for capturing or determining EDA data are described in co-pending application entitled DETECTION AND RESPONSE TO AROUSAL ACTIVATIONS, which is incorporated herein in its entirety for all purposes.
  • Sympathetic nervous system activity causes perspiration, and EDA measures the amount of conductance across the user’s skin to quantify current amounts of SNS activity.
  • This metric does not measure PNS in at least some embodiments, and so it may not provide a true measure of sympathovagal balance, rather just SNS activity, unlike other heart-related metrics.
  • a feature value can relate to EDA activity during meditation and check-in sessions.
  • a user has logged meditation or “check-in” sessions using the EDA session, then their average EDA score across all sessions can be compared with their baseline value and the feature can receive a score of, for example, 0, 1, or 2 points. If no sessions were logged, they may receive 1 point. In one embodiment, users who did not log EDA that day, may get 1 point, while users who did a guided EDA session get 2 points (regardless of alignment), and users who did an unguided EDA session, use an average of the session relative to the last 30 days of valid EDA sessions. If session is higher than average, those users get 0 points. If the session is around average, the users get 1 point. If session is less than the average, the users get 2 points.
  • a weighting of the EDA in a stress score calculation can vary, as may depend in part upon factors such as an accuracy of the EDA values or a relative importance of that data for an individual user.
  • EDA can serve as a proxy for quantifying the amount of sympathetic nervous system activity. This data can represent this activity happening momentarily.
  • the sympathetic nervous system can trigger micro-perspiration throughout a person’s body, so the conductance between a sensor and a hand or fingertip of a user will increase as the perspiration levels increase. When greater conductance is detected, this can be representative of higher sympathetic nervous system activity.
  • at least two different EDA metrics can be monitored.
  • a first metric is a tonal metric called skin conductance level, which looks at the absolute level over time, and whether that value is increasing or decreasing.
  • a second metric represents a skin conductance response (SCR), which looks at the number of spikes in the skin conductance within a sliding window of time, such as a window of one minute in duration. SCR thus can represent a count per minute of spikes in the EDA conductance level.
  • SCR skin conductance response
  • a continuous EDA determination can be made for such purposes, while a discrete or periodic EDA signal may not support such granular determinations.
  • an algorithm can utilize at least some of these and/or other such features to generate a stress score that is representative of a current, past, or future stress state of a user.
  • a system or service utilizing such a score can provide a real-time metric that can be correlated with physical and/or perceived stress.
  • Such a system may provide for manual input by a user, such has may relate to the collection of physical or perceived stress-related data.
  • such a system can capture perceived stress scale (PSS) survey results measuring chronic stress on a broad distribution of users.
  • PSS perceived stress scale
  • Such a system can also generate a daily physiological stress and/or stress capacity metric.
  • an algorithm can calculate stress scores that represent an “expert guided” determinations of physiological stress that can be inverted to reflect stress capacity and/or resilience.
  • low stress capacity or resilience scores can indicate high levels of stress, while high resilience scores can indicate readiness for the cognitive/emotional/physical demands of the day.
  • FIG. 4 illustrates example displays or interfaces that can be provided to a user in accordance with at least one embodiment.
  • a first interface 400 provides information including a stress score field, as well as an option to obtain additional stress data.
  • a second interface 410 provides a set of stress scores plotted over time, in this case over a certain week. Such information can help a user to identify trends, as well as to help to correlate events of different days with different stress levels or scores. As illustrated, a user may be able to provide feedback for different levels of stress, which can also be plotted by day for comparison.
  • a third interface 420 can provide other information, such as mood, over that week or period of time. In at least one embodiment, there may be various sub-scores or components to a stress score, as may relate to responsiveness, exertion balance, or sleep patterns or scores.
  • a fourth interface 430 can enable a user to provide feedback about their current mood or state.
  • FIG. 5 illustrates additional interfaces that can be provided to a user in accordance with another embodiment.
  • each interface presents information that is related to stress resilience, rather than a stress score that might be interpreted as an absolute level of stress by a user.
  • a first interface 500 can present a stress resilience score, as well as a last presented stress state (and a time at which that state was presented).
  • a second interface 510 can be presented to a user who has not yet started entering or obtaining stress resilience data, such as where at least some data or permission may be required from that user before presentation.
  • a third interface 520 provides a different view of stress resilience over time, including data for individual stress resilience components as discussed previously. Such an interface can also allow a user to provide new, additional, or updated feedback that can be used in determining such values for presentation.
  • FIG. 6 illustrates additional interfaces that can be provided to a user in accordance with still another embodiment.
  • a first interface page 600 presents another view of stress resilience data over time, particularly presenting distributions of stress levels or states for different days, rather than presenting resilience values.
  • a second interface 610 presents information that helps a user to understand these scores, what goes into them, and what different scores represent.
  • Various other data and interfaces can be used as well in accordance with various embodiments.
  • data can be broken down into three stress score groups, namely an exertion group, a heart group, and a sleep pattern group.
  • the exertion group can include data for weekly activity, daily steps, and fitness fatigue score, or exertion balance.
  • the heart group can include elevated HR at rest, sleeping HR above RHR, deep sleep HRV, and potentially EDA. This data can be representative of a user’s nervous system, responsiveness, neural stimulation, neural gauge, and stimulation.
  • the sleep pattern group can include data about sleep restlessness, sleep fragmentation, deep sleep latency, deep and REM sleep duration, and sleep reservoir level.
  • a stress score can have values that range from 0 to 100, where a value of 100 can mean that a user’s body has been showing signs of a lot of stress. Alternatively, a stress resilience score of 100 might mean that a user is showing little to no signs of stress. Other values or metrics can be used as well.
  • Such interfaces and information can attempt to provide a holistic management tool. Such an approach can thus analyze both physical stress and mental stress.
  • An interface can be provided that quickly enables a user to obtain their daily or current stress score, along with other scores such as sleep scores and the like.
  • Such information can also help a user to reflect on their mood and remind the user to log or provide that information.
  • a user can also access additional data, such as a stress detail page where a user can obtain additional information about a current stress state or score, as well as the various components used for that determination.
  • a user may be able to drill into data components to obtain additional information of interest.
  • sensors and devices may be able to provide data about physical stress, but a user may be the best source of mental stress data, at least for certain types of mental stress data.
  • a user may be able to log a current mood or perceived stress level, or provide other such information.
  • a user can be prompted to enter mood or stress data after an EDA scan to provide for improved correlation. Such an approach can help to incorporate EDA data into a holistic view of a user’s physical and mental health.
  • a device can provide for periodic or continuous EDA measurements, which can be used to dynamically update stress determinations over time.
  • a stress score determination algorithm considers various factors that may impact a user’s stress level.
  • the weighting of these factors can be determined across users, or different ty pes of users. In at least some embodiments these weightings can also be adapted for individual users to improve accuracy.
  • a sleep stages algorithm can be used to differentiate periods of sleep, which may have significant impact on stress levels for certain users.
  • looking at factors such as HRV in specific sleep states versus an entire night can provide additional insight.
  • combined deep and REM sleep duration can provide valuable insight as these periods are generally more restorative. There can be a significant difference between getting eight hours of light sleep versus four hours of light sleep and four hours of deep sleep and REM sleep.
  • mental stress factors may impact different users more heavily than physical stress factors, both of which can be considered by such an algorithm. Additional benefit can be obtained by looking at different types of metrics across different domains of exercise or exertion, sleep, and proxies for autonomic nervous system activity' both with heart rate/heart rate variability as well as EDA or other such data. A useful benefit for a user can also be comparing physical to perceived stress levels, so a user can better understand their stress.
  • a stress determination can be a linear or non-linear combination of weighted and normalized factors, where those factors may be normalized based on personal, demographic, or other such groupings.
  • some factors may need to be inverted where some represent higher stress levels while others represent lower stress levels.
  • inverted factors include deep and REM sleep duration, sleep reservoir level, and fitness fatigue score.
  • Some factors can utilize a z-score-based approach, where a z-score of 1 represents one standard deviation above the mean, etc.
  • factors can also be normalized over different periods of time and different groupings, such as per user or per demographic group.
  • a ranging function can be applied after z-scoring to put all values into a determined range, such as between 0 and 1. In some embodiments this can involve a linear rectification and interpolation.
  • stress scores can be determined such that a single score, such as 80 on a scale of 100, represents the same stress level, or stress resilience, for all users.
  • values may mean different things to different users, such as where a first user might have an average stress level of 50 while another user might have an average stress level of 80, such that a value of 70 might mean different things to those two users.
  • a user who is very active might have a different algorithm utilized than a user who is not active, while different algorithms may also be utilized for different devices where different ty pes of input are available, or where a user may have an option of deactivating certain sensors or restricting types of data from being collected.
  • at least three categories of factors can be collected, including sleep feature, activity features, and heart features (or “responsiveness” features).
  • EDA or similar data may be utilized as well.
  • factors within these categories that may be utilized can include restlessness, fragmentation, sleep reservoir level, deep/REM sleep duration, deep sleep latency, active zone minutes or activity level, step count or movement, deep sleep HRV, elevated HR at rest, sleeping HR above RHR, and fitness fatigue score.
  • Other factors can include various exercise or activity metrics, as well as exertion balance metrics.
  • Additional factors can include blood pressure, blood composition, respiration rate, temperature, metabolic data, blood sugar levels, body weight or composition, psychological state, perceived stress, depression, activity type, or current movement patterns (e.g., gait).
  • LDL low-density lipoprotein
  • the process 700 includes activating stress determination for a user associated with a wearable device. This activation can come from a user, the wearable device, or an associated device, among other such sources.
  • the process 700 includes receiving data, from one or more sensors or components on the wearable device, that relate to a state of the user, such as may relate to heart rate, sleep state, EDA, activity , or other such information discussed and suggested herein.
  • the process 700 includes obtaining additional data provided by the user, such as may relate to perceived state data of the user.
  • the process 700 includes calculating a stress score (or stress resilience score) for that user. This stress score or value can relate to various stress metrics, such as a current stress level or stress resilience level of the user.
  • the process 700 includes performing at least one action on the wearable device (or an associated device) based at least in part upon this calculated score.
  • These actions can include any of a variety of different actions, as may relate to generating an interface, presenting data, providing a notification, updating, or modifying an operation of the wearable device, or performing another such action.
  • FIG. 8 illustrates another example process 800 for monitoring stress for a user that can be utilized in accordance with various embodiments.
  • the process 800 includes activating stress monitoring for a user associated with a wearable device. An initial stress determination can be performed, such as described with respect to FIG. 7.
  • the process 800 includes receiving new or updated sensor data and/or user-provided data.
  • the process 800 includes calculating an updated stress score based at least in part upon this new or updated data.
  • the process 800 includes analyzing change in stress score, such as with respect to an immediately prior value determination.
  • the process 800 includes determining whether the change is an actionable change, such as a change that exceeds a change threshold, falls outside an acceptable range, or satisfies an action threshold. If not, then the process 800 can continue with new and updated data being received. If the change is determined to be an actionable change, then at least one action can be performed, as shown at (812) that corresponds to the change, where those actions can include those discussed with respect to the initial stress score calculation above.
  • an actionable change such as a change that exceeds a change threshold, falls outside an acceptable range, or satisfies an action threshold. If not, then the process 800 can continue with new and updated data being received. If the change is determined to be an actionable change, then at least one action can be performed, as shown at (812) that corresponds to the change, where those actions can include those discussed with respect to the initial stress score calculation above.
  • FIG. 9 illustrates components of an example system 900 that can be utilized in accordance with various embodiments.
  • the system 900 includes at least one processor 902, such as a central processing unit (CPU) or graphics processing unit (GPU) for executing instructions that can be stored in a memory device 904, such as may include flash memory or DRAM, among other such options.
  • the device can include many types of memory, data storage, or computer-readable media, such as data storage for program instructions for execution by a processor. The same or separate storage can be used for images or data, a removable memory can be available for sharing information with other devices, and any number of communication approaches can be available for sharing with other devices.
  • the system 900 includes any suitable display 906, such as a touch screen, organic light emitting diode (OLED), or liquid crystal display (LCD), although devices might convey information via other means, such as through audio speakers or projectors.
  • OLED organic light emitting diode
  • LCD liquid crystal display
  • a tracker or similar device includes at least one motion detection sensor, which as illustrated can include at least one input/ output (I/O) element 910 of the device.
  • I/O input/ output
  • Such a sensor can determine and/or detect orientation and/or movement of the system 900.
  • Such an element can include, for example, an accelerometer, inertial sensor, altimeter, or gyroscope operable to detect movement (e.g., rotational movement, angular displacement, tilt, position, orientation, motion along a non-linear path, etc.) of the device.
  • An orientation determining element can also include an electronic or digital compass, which can indicate a direction (e.g., north or south) in which the device is determined to be pointing (e.g., with respect to a primary axis or other such aspect).
  • the I/O element 910 may also be used for determining a location of the device (or the user of the device).
  • a positioning element can include a GPS or similar location-determining element(s) operable to determine relative coordinates for a position of the device.
  • Positioning elements may include wireless access points, base stations, etc., that may either broadcast location information or enable triangulation of signals to determine the location of the device.
  • Other positioning elements may include QR codes, barcodes, RFID tags, NFC tags, etc., that enable the device to detect and receive location information or identifiers that enable the device to obtain the location information (e.g., by mapping the identifiers to a corresponding location).
  • Various embodiments can include one or more such elements in any appropriate combination.
  • the I/O elements 910 may also include one or more biometric sensors, optical sensors, barometric sensors (e.g., altimeter, etc.), and the like.
  • some embodiments use the element(s) to track the location and/or motion of a user.
  • the device of some embodiments may keep track of the location of the device by using the element(s), or in some instances, by using the orientation determining element(s) as mentioned above, or a combination thereof.
  • the algorithms or mechanisms used for determining a position and/or orientation can depend at least in part upon the selection of elements available to the device.
  • the example device also includes one or more wireless components 912 operable to communicate with one or more electronic devices within a communication range of the particular wireless channel.
  • the wireless channel can be any appropriate channel used to enable devices to communicate wirelessly, such as Bluetooth, cellular, NFC, or Wi-Fi channels. It should be understood that the system 900 can have one or more conventional wired communications connections as known in the art.
  • the system 900 also includes one or more power components 908, such as may include a battery operable to be recharged through conventional plug-in approaches, or through other approaches such as capacitive charging through proximity with a power mat or other such device.
  • the system 900 can include at least one additional I/O device 910 able to receive conventional input from a user.
  • This conventional input can include, for example, a push button, touch pad, touch screen, wheel, joystick, keyboard, mouse, keypad, or any other such device or element whereby a user can input a command to the device.
  • I/O devices could even be connected by a wireless infrared or Bluetooth or other link as well in some embodiments.
  • Some devices also can include a microphone or other audio capture element that accepts voice or other audio commands.
  • a device might not include any buttons at all, but might be controlled only through a combination of visual and audio commands, such that a user can control the device without having to be in contact with the device.
  • many embodiments include at least some combination of one or more emitters 916 and one or more detectors 918 for measuring data for one or more metrics of a human body, such as for a person wearing the tracker device.
  • this may involve at least one imaging element, such as one or more cameras that are able to capture images of the surrounding environment and that are able to image a user, people, or objects in the vicinity of the device.
  • the image capture element can include any appropriate technology, such as a CCD image capture element having a sufficient resolution, focal range, and viewable area to capture an image of the user when the user is operating the device. Methods for capturing images using a camera element with a computing device are well known in the art and will not be discussed herein in detail.
  • image capture can be performed using a single image, multiple images, periodic imaging, continuous image capturing, image streaming, etc.
  • a device can include the ability to start and/or stop image capture, such as when receiving a command from a user, application, or other device.
  • the emitters 916 and detectors 918 of FIG. 9 may also be capable of being used, in one example, for obtaining optical photoplethsymogram (PPG) measurements.
  • PPG optical photoplethsymogram
  • Some PPG technologies rely on detecting light at a single spatial location, or adding signals taken from two or more spatial locations. Both of these approaches result in a single spatial measurement from which the heart rate (HR) estimate (or other physiological metrics) can be determined.
  • HR heart rate
  • a PPG device employs a single light source coupled to a single detector (i.e., a single light path).
  • a PPG device may employ multiple light sources coupled to a single detector or multiple detectors (i.e., two or more light paths).
  • a PPG device employs multiple detectors coupled to a single light source or multiple light sources (i.e., two or more light paths).
  • the light source(s) may be configured to emit one or more of green, red, and/or infrared light.
  • a PPG device may employ a single light source and two or more light detectors each configured to detect a specific wavelength or wavelength range.
  • each detector is configured to detect a different wavelength or wavelength range from one another.
  • two or more detectors configured to detect the same wavelength or wavelength range.
  • one or more detectors configured to detect a specific wavelength or wavelength range different from one or more other detectors).
  • the PPG device may determine an average of the signals resulting from the multiple light paths before determining an HR estimate or other physiological metrics. Such a PPG device may not be able to resolve individual light paths or separately utilize the individual signals resulting from the multiple light paths.
  • system 900 may further include one or more processors 902 coupled to memory device 904, display 906, bus, one or more input/output (I/O) elements 910, and wireless networking components 912, among other such options.
  • processors 902 coupled to memory device 904, display 906, bus, one or more input/output (I/O) elements 910, and wireless networking components 912, among other such options.
  • a display and/or I/O devices may be omitted.
  • the system 900 may be part of a wristband and the display 906 is configured such that the display faces away from the outside of a user’s wrist when the user wears the wristband.
  • the display may be omitted and data detected by the system 900 may be transmitted using the wireless networking interface via near-field communication (NFC), Bluetooth, Wi-Fi, or other suitable wireless communication protocols over at least one network 920 to a host computer 922 for analysis, display, reporting, or other such use.
  • NFC near-field communication
  • Wi-Fi Wireless Fidelity
  • the memory 904 may include RAM, ROM, FLASH memory, or other non- transitory digital data storage, and may include a control program comprising sequences of instructions which, when loaded from the memory and executed using the processor 902, cause the processor 902 to perform the functions that are described herein.
  • the emitters 916 and detectors 918 may be coupled to a bus directly or indirectly using driver circuitry by which the processor 902 may drive the emitters 916 and obtain signals from the detectors 918.
  • the host computer 922 can communicate with the wireless networking components 912 via the one or more networks 920, which may include one or more local area networks, wide area networks, and/or internetworks using any of terrestrial or satellite links. In some embodiments, the host computer 922 executes control programs and/or application programs that are configured to perform some of the functions described herein.
  • each emitter 916 can be individually controlled, or each detector 918 can be individually read out when multiple detectors are used, and in such embodiments, PPG sensor data along several different light paths can be collected.
  • the control program can utilize the collected data to provide a more accurate estimation or HR and/or other physiological metrics.
  • the processor 902 and other component(s) of the PPG device may be implemented as a System-on-Chip (SoC) that may include one or more central processing unit (CPU) cores that use one or more reduced instruction set computing (RISC) instruction sets, and/or other software and hardware to support the PPG device.
  • SoC System-on-Chip
  • CPU central processing unit
  • RISC reduced instruction set computing
  • the emitters 916 may include electronic semiconductor light sources, such as LEDs, or produce light using any of filaments, phosphors, or laser.
  • each of the light sources emits light having the same center wavelength or within the same wavelength range.
  • at least one light source may emit light having a center wavelength that is different from another one of the light sources.
  • the center wavelengths of the light emitted by the light sources may be in the range of 495 nm to 570 nm. For example, a particular green light source may emit light with a center wavelength of 528 nm.
  • one or more of the light sources may emit red light (e g., 660 nm center wavelength) or IR light (e g., 940 nm center wavelength).
  • one or more of the light sources may emit light with peak wavelengths typically in the range of 650 nm to 940 nm.
  • a particular red light source may emit light with a peak wavelength of 660 nm
  • one or more infrared light sources may emit light with peak wavelengths in the range of 750 nm to 1700 nm.
  • a particular infrared light source may emit light with a peak wavelength of 730 nm, 760 nm, 850 nm, 870 nm, or 940 nm.
  • commercial light sources such as LEDs may provide output at about 20 nm intervals with a center wavelength tolerance of +/- 10 nm from the manufacturer’s specified wavelength and thus one possible range of useful peak wavelengths for the light sources is 650 nm to 950 nm.
  • the green light sources may be configured to emit light with wavelengths in the range of 495 nm to 570 nm.
  • a particular green light source may emit light with a wavelength of 528 nm.
  • the green light sources may be equally spaced from light detectors as the pairs of red and infrared light sources. For example, if the distance between light detectors and a center of a first red light source is 2 mm, the distance between light detectors and a green light source may also be 2 mm (e.g., equidistant). In some other cases, the distance between the light detectors and one or more light sources is not equidistant. Further, in some embodiments, one or more of the light sources may comprise a single LED package that emits multiple wavelengths, such as green, red, and infrared wavelengths, at the same or substantially the same (e.g., less than 1 mm difference) location with respect to multiple detectors. Such LEDs may include multiple semiconductor elements co-located using a single die in a single package.
  • the spacing of the light sources may be measured from the side of the light source or the center of the light source.
  • the light sources may be configured such that the center of each light source is at a first distance from the edge of the closest one of the light detectors.
  • the first distance may be 2 mm.
  • each light source is located at a second distance from the closest one of the light sources, and each light detector is located at a third distance from the closest one of the light detectors.
  • the second and third distances are identical to the first distance.
  • each of the second and third distances is different from the first distance.
  • the second distance may be identical to or different from the third distance.
  • the particular magnitude of the spacing may depend on a number of factors and this disclosure does not limit the embodiments to any particular spacing. For example, spacing in a range of 1 mm (or less) to 10 mm would be workable in various embodiments.
  • independent control of all light sources is provided.
  • several light sources are controlled together as a gang or bank.
  • a benefit of independent control of each light source, or independent readout from each of multiple detectors is that a multiple light path approach may be used to improve the estimation of HR and/or other physiological metrics, as discussed further herein.
  • Light detectors may include one or more sensors that are adapted to detect wavelengths of light emitted from the light sources.
  • a particular light source combined with a particular detector may comprise a sensor such as a PPG sensor.
  • a first PPG sensor and a second PPG sensor can share components, such as the same light sources and/or detectors, or have different components and thus the term “PPG sensor,” in addition to having its ordinary meaning, may refer to any of such arrangements although actual embodiments may use multiple components in implementing a PPG sensor.
  • the term “PPG device,” in addition to having its ordinary meaning, may refer to a device including a PPG sensor.
  • a light detector in an embodiment, may comprise one or more detectors for detecting each different wavelength of light that is used by the light sources.
  • a first detector may be configured to detect light with a wavelength of 560 nm
  • a second detector may be configured to detect light with a wavelength of 940 nm
  • a third detector may be configured to detect light with a wavelength of 528 nm.
  • Examples include photodiodes fabricated from semiconductor materials and having optical filters that admit only light of a particular wavelength or range of wavelengths.
  • the light detectors may comprise any of a photodiode, phototransistor, charge-coupled device (CCD), thermopile detector, microbolometer, or complementary metal-oxide-semiconductor (CMOS) sensor.
  • the light detectors may comprise multiple detector elements, as further described herein. One or more of the detectors may comprise a bandpass filter circuit.
  • a detector may comprise one or more detectors configured to detect multiple wavelengths of light.
  • a single detector may be configured to tune to different frequencies based on data received from an electrical digital microprocessor coupled to detectors.
  • the single detector may include multiple active areas where each active area is sensitive to a given range of wavelengths.
  • a single detector is configured to detect light with wavelengths in the red and IR frequencies and a second detector is configured to detect light with wavelengths in the green frequencies.
  • each of the light sources may use any of one or more different wavelengths of light as previously described.
  • light detectors can be mounted in a housing with one or more filters that are configured to filter out wavelengths of light other than wavelengths emitted by light sources.
  • a portion of the housing may be covered with a filter which removes ambient light other than light in wavelengths emitted by light sources.
  • signals from light sources may be received at the light detectors through an ambient light filter that filters out an ambient light source that generates an ambient light with a wavelength that is different from the wavelength that is detected by the detector.
  • LEDs and photodiodes are used as examples of the light sources and the light detectors, respectively, the techniques described herein may be extended to other types of light sources.
  • the PPG device may include (i) single or multiple LEDs and a multi-element photodetector (e.g., a camera sensor), (ii) an LED array and single or multiple photodiodes, (iii) a broadband LED-pumped phosphor and detector array with wavelength selective filters on each detector, (iv) spatial light modulator (SLM) (e.g., a digital micromirror device [DMD] or a liquid crystal on silicon [LCoS] device) and single or multiple LEDs, other combinations thereof, or other configurations of light sources and detectors.
  • SLM spatial light modulator
  • Various embodiments may be coded using assembly, C, OBJECTIVE-C, C++, JAVA, or other human-readable languages and then compiled, assembled, or otherwise transformed into machine code that can be loaded into ROM, EPROM, or other recordable memory of the activity monitoring apparatus that is coupled to the CPU or microcontroller and then then executed by the CPU or microcontroller.
  • signals obtained from multiple light paths may be processed to filter or reject signal components that are associated with motion of the user, using a computer program to identify the motion component of the signal and remove the identified motion component from the composite signal, leaving the cardiac component as a remainder or final signal.
  • signals might be collected in variety of activities during day or at night, such as may relate to periods of walking, exercise, or sleep.
  • Other on-device sensors including an accelerometer, gyroscope, or altimeter may be used to categorize or detect the activity, or human posture as a basis to develop the appropriate filters.
  • These filters or signal processing methods might be used for targeted reduction of variability in the PPG data with multiple light paths.
  • the accelerometer data can be used to develop signal processing methods to filter the data and look into a certain posture, removing other body orientations. This can help reduce the noise in the data and get a better assessment of the corresponding physiological variables for the corresponding light paths.
  • approaches discussed herein may be performed by one or more of: firmware operating on a monitoring or tracker device or a secondary device, such as a mobile device paired to the monitoring device, a server, host computer, and the like.
  • the monitoring device may execute operations relating to generating signals that are uploaded or otherwise communicated to a server that performs operations for removing the motion components and creating a final estimate value for HR, SpCh, and/or other physiological metrics.
  • the monitoring device may execute operations relating to generating the monitoring signals and removing the motion components to produce a final estimate value for HR, SpCh, and/or other physiological metrics local to the monitoring device.
  • the final estimate may be uploaded or otherwise communicated to a server such as host computer that performs other operations using the value.
  • An example monitoring or tracker device can collect one or more types of physiological and/or environmental data from one or more sensor(s) and/or external devices and communicate or relay such information to other devices (e.g., host computer or another server), thus permitting the collected data to be viewed, for example, using a web browser or network-based application.
  • a tracker device may perform biometric monitoring via calculating and storing the user’s step count using one or more sensor(s).
  • the tracker device may transmit data representative of the user’s step count to an account on a web service (e.g., www.fitbit.com), computer, mobile phone, and/or health station where the data may be stored, processed, and/or visualized by the user.
  • a web service e.g., www.fitbit.com
  • the tracker device may measure or calculate other physiological metric(s) in addition to, or in place of, the user’s step count.
  • physiological metric(s) may include, but are not limited to: energy expenditure, e.g., calorie bum; floors climbed and/or descended; HR; heartbeat waveform; HR variability; HR recovery; respiration, SpCh, blood volume, blood glucose, skin moisture and skin pigmentation level, location and/or heading (e.g., via a GPS, global navigation satellite system (GLONASS), or a similar system); elevation; ambulatory speed and/or distance traveled; swimming lap count; swimming stroke type and count detected; bicycle distance and/or speed; blood glucose; skin conduction; skin and/or body temperature; muscle state measured via electromyography; brain activity as measured by electroencephalography; weight; body fat; caloric intake; nutritional intake from food; medication intake; sleep periods (e.g., clock time, sleep phases, sleep quality and/or duration); pH levels; hydration levels; respiration rate; and/or other physiological
  • An example tracker or monitoring device may also measure or calculate metrics related to the environment around the user (e.g., with one or more environmental sensor(s)), such as, for example, barometric pressure, weather conditions (e.g., temperature, humidity, pollen count, air quality, rain/snow conditions, wind speed), light exposure (e.g., ambient light, ultra-violet (UV) light exposure, time and/or duration spent in darkness), noise exposure, radiation exposure, and/or magnetic field.
  • a tracker device and/or the host computer and/or another server
  • a tracker device may calculate the user’s stress or relaxation levels based on a combination of HR variability, skin conduction, noise pollution, and/or sleep quality.
  • a tracker device may determine the efficacy of a medical intervention, for example, medication, based on a combination of data relating to medication intake, sleep, and/or activity.
  • a tracker device may determine the efficacy of an allergy medication based on a combination of data relating to pollen levels, medication intake, sleep and/or activity.
  • An example monitoring device may include a computer-readable storage media reader, a communications device (e.g., a modem, a network card (wireless or wired), an infrared communication device) and working memory as described above.
  • the computer- readable storage media reader can be connected with, or configured to receive, a computer- readable storage medium representing remote, local, fixed and/or removable storage devices as well as storage media for temporarily and/or more permanently containing, storing, transmitting, and retrieving computer-readable information.
  • a monitoring system and various devices also typically will include a number of software applications, modules, services, or other elements located within at least one working memory device, including an operating system and application programs such as a client application or Web browser.
  • Storage media and other non-transitory computer readable media for containing code, or portions of code can include any appropriate media known or used in the art, such as but not limited to volatile and non-volatile, removable and non-removable media implemented in any method or technology for storage of information such as computer readable instructions, data structures, program modules or other data, including RAM, ROM, EEPROM, flash memory or other memory technology, CD-ROM, digital versatile disk (DVD) or other optical storage, magnetic cassettes, magnetic tape, magnetic disk storage or other magnetic storage devices or any other medium which can be used to store the desired information and which can be accessed by a system device.
  • RAM random access memory
  • ROM read only memory
  • EEPROM electrically erasable programmable read-only memory
  • flash memory electrically erasable programmable read-only memory
  • CD-ROM compact disc read-only memory
  • DVD digital versatile disk
  • magnetic cassettes magnetic tape
  • magnetic disk storage magnetic disk storage devices or any other medium which can be used to store the desired information and which can be
  • FIG. 10 a flow diagram of a computer-implemented method 1000 for determining a fitness fatigue score for a user for a current day (e.g., today) is provided according to embodiments of the present disclosure.
  • the method 1000 can be implemented by, for instance, the system 900 discussed above with reference to FIG. 9. More particularly, one or more steps of the method 1000 can be performed by the processor 902 (FIG. 9) on the wearable computing device (e.g., smart watch 104 or 202). Alternatively, or additionally, one or more steps of the method 1000 can be performed by a computing device (e.g., host computer 922 of FIG. 9) that is remote relative to the smart watch.
  • the method 1000 can include obtaining first data for the user over a first period of time.
  • the first data can include a plurality of heart rate measurements for the user over the first period of time.
  • the first period of time can include the 14 days (e.g., two weeks) immediately prior to the current day for which the fitness fatigue score is being determined.
  • the method 1000 can include obtaining second data for the user over a second period of time that is shorter in duration than the first period of time.
  • the second data can include one or more sleep metrics for a plurality of different sleep events for the user over the second period of time.
  • the one or more sleep metrics can include a duration of each of the sleep events and a time of day at which each of the sleep events occurred.
  • the second period of time can include the 7 days (e.g., one week) immediately prior to the current day for which the fitness fatigue score is being determined.
  • the method 1000 can include obtaining third data for the user over a third period of time that is longer in duration than the first period of time.
  • the third data can include heart rate variability for the user over the third period of time.
  • the third period of time can include the 30 days (e.g., one month) immediately prior to the current day for which the fitness fatigue score is being determined.
  • the method 1000 can include determining the fitness fatigue score for the user for the current day based, at least in part, on the first data obtained at (1002), the second data obtained at (1004), and the third data obtained at (1006).
  • the fitness fatigue score can include a numerical value ranging from 0 to 100.
  • the method 1000 can include causing a display screen of an electronic device to display the fitness fatigue score determined at (1008).
  • the fitness fatigue score can be displayed on a display screen of a wearable device (e.g., smart watch 104 in FIG. 1A and 202 in FIG. 2) worn by the user.
  • the fitness fatigue score can be displayed on a display screen of a mobile computing device (e.g., smartphone 204 or tablet 206 in FIG. 2) that is communicatively coupled to the wearable computing device.
  • the method 1000 can include determining a recommendation regarding exercise for the current day based, at least in part, on the fitness fatigue score determined at (1010) for the current day.
  • the recommendation can vary depending on the fitness fatigue score.
  • a first threshold value e.g., about 30
  • the recommendation can include foregoing exercise (e.g., resting) for the current day.
  • the recommendation can include a first exercise activity (e.g., low heart-rate exercise).
  • the recommendation can include a second exercise activity (e g., high-intensity cardio) that is more strenuous than the first exercise activity when the fitness fatigue score determined at (1008) is greater than the second threshold value.
  • FIG. 11 a flow diagram of a method 1100 for determining the fitness fatigue score according to some embodiments of the present disclosure is provided.
  • the method 1100 can be implemented by, for instance, the system 900 discussed above with reference to FIG. 9. More particularly, one or more steps of the method 1000 can be performed by the processor 902 (FIG. 9) on the wearable computing device (e.g., smart watch 104 or 202). Alternatively, or additionally, one or more steps of the method 1000 can be performed by a computing device (e.g., host computer 922 of FIG. 9) that is remote relative to the smart watch.
  • FIG. 11 depicts steps performed in a particular order for purposes of illustration and discussion. Those of ordinary skill in the art, using the disclosures provided herein, will understand that various steps of the method 1100 may be adapted, modified, rearranged, performed simultaneously, or modified in various ways without deviating from the scope of the present disclosure.
  • the method 1100 can include determining a first subscore (e.g., H-score) based, at least in part, on the first data obtained at (1002) of the method 1000 depicted in FIG. 10.
  • the first subscore can be determined based, at least in part, on the plurality of heart rate measurements the one or more biometric sensors of the wearable computing device worn by the user capture over the first period of time (e.g., about 14 days).
  • the first subscore can be determined based, at least in part, on an amount of time the heart rate measurements collected for the user over the first period of time were above a threshold value indicative of the user being stressed (e.g., due to exercise).
  • a number of minutes the user’s heart rate was above the threshold value can be determined and then the first subscore can be determined therefrom. More particularly, if the heart rate data was above a threshold value for a threshold amount of time yesterday, this can indicate that the user engaged in a strenuous physical activity (e.g., running, swimming, etc.) yesterday and therefore may be fatigued from the physical activity. It should be appreciated that the threshold heart rate can be specific to the user based, at least in part, on the user’s resting heart rate and the user’s maximum heart rate that is a function of the user’s age.
  • the method 1100 can include determining a second subscore (e.g., S- score) based, at least in part, on the second data obtained at (1004) of the method 1000 depicted in FIG. 10.
  • the second subscore can be determined based, at least in part, on the one or more sleep metrics for each of a plurality of sleep events for the user that occurred during the second period of time (e.g., about 7 days).
  • the one or more sleep metrics can include a duration of each of the plurality of sleep events.
  • the one or more sleep metrics can include a time of day at which each of the sleep events started and ended.
  • the second subscore can be high when the user gets at least a threshold number of hours (e.g., about 7 hours) of sleep each night. Conversely, the second subscore can be low when the user gets less than the threshold number of hours of sleep each night.
  • the second subscore can be a function of an amount of time the user spends in one or more sleep stages for one or more of the plurality of sleep events occurring over the second period of time (e.g., 7 days). For instance, the second subscore can be higher when the user spends a threshold amount of time in a restorative stage (e.g., deep sleep or rapid eye movement) of sleep for one or more of the sleep events. It should be understood that the threshold amount of time needed in the restorative stage of sleep can be a function of the user’s age.
  • the second subscore can be a function of the time of day for one or more of the sleep events during the second period of time (e.g., 7 days). For instance, if the second data indicates the user takes naps during the day and as a result sleeps less at night, the second subscore can be lower than if the user took no naps and slept for longer each night.
  • the method 1100 can include determining a third subscore (e.g., T-score) based, at least in part, on the third data obtained at (1006) of the method 1000 depicted in FIG. 10. Details of this step will be discussed in more detail with reference to FIG. 13.
  • a third subscore e.g., T-score
  • the method 1100 can include determining the fitness fatigue score based, at least in part, on the first subscore (e.g., H-score), the second subscore (e.g., S-score), and the third subscore (e.g., T-score).
  • the first subscore, the second subscore, and the third subscore can each include a numerical value ranging from 0 to 100.
  • the first subscore determined at (1102), the second subscore determined at (1104), the third subscore determined at (1106) can each be weighted differently.
  • the first subscore e.g., H-score
  • the second subscore e.g., S-score
  • T- score the third subscore
  • the first subscore can account for half of the fitness fatigue score.
  • the fitness fatigue score can be the first subscore.
  • the fitness fatigue score can be the first subscore when the first subscore is below a threshold value (e.g., about 30).
  • FIG. 12 a flow diagram of method 1200 for determining the first subscore (e.g., H score) of the fitness fatigue score is provided according to embodiments of the present disclosure.
  • the method 1200 can be implemented by, for instance, the system 900 discussed above with reference to FIG. 9.
  • FIG. 12 depicts steps performed in a particular order for purposes of illustration and discussion. Those of ordinary skill in the art, using the disclosures provided herein, will understand that various steps of the method 1200 may be adapted, modified, rearranged, performed simultaneously, or modified in various ways without deviating from the scope of the present disclosure.
  • the method 1200 can include determining a resting heart rate of the user based, at least in part, on the plurality of heart rate measurements included in the first data obtained over the first period of time.
  • the method 1200 can include determining a maximum heart rate of the user based, at least in part, on the user’s age. For instance, in some embodiments, the maximum heart rate of the user can be determined by subtracting the user’s age from 220 beats per minute. For example, if the user is 40 years old, the user’s maximum heart rate can be 180 beats per minute.
  • the method 1200 can include determining a reserve value for each of the plurality of heart rate measurements included in the first data obtained over the first period of time.
  • the reserve value can be used to differentiate between heart rate measurements when the user is sedentary (e.g., sleeping, sitting, etc.) from heart rate measurements when the user is engaging in physical activity (e.g., running, walking, cycling, yoga, etc.).
  • the heart rate reserve value can be determined based, at least in part, on the resting heart rate of the user determined at (1202), the maximum heart rate of the user determined at (1204), and an instantaneous heart rate of the user (that is, one of the plurality of heart rate measurements).
  • the reserve value can be a numerical value ranging from 0 to 1.
  • the method 1200 can determine a subset of the plurality of heart rate measurements are associated with physical activity based, at least in part, on the reserve values determined at (1206). For instance, in some embodiments, heart rate measurements having a reserve value that is below a threshold value (e.g., about 0.4) can be ignored whereas the subset of heart rate measurements having a reserve value that is equal to or greater than the threshold value can be used to determine the first subscore. In this manner, the reserve value can reduce the amount of data (e.g., heart rate measurements) that must be considered in order to determine the first subscore indicative of fatigue of the user due to physical activity over the first period of time.
  • a threshold value e.g., about 0.4
  • the method 1200 can include determining the first subscore based, at least in part, on the subset of heart rate measurements included in the first data. For instance, in some embodiments, a duration of time during which the heart rate reserve value for the user’s heart rate was above the threshold value can be determined. Furthermore, in some embodiments, an amount of time that has lapsed since the heart rate reserve value for the user’s heart rate was above the threshold value can be determined. In some embodiments, the first subscore can be determined based, at least in part, on one or both of these parameters (e.g., duration of time during which the heart rate reserve value was above the threshold value, duration of time since the heart rate reserve value for the user’s heart rate was last above the threshold value). Alternatively, or additionally, the first subscore can, in some embodiments, include a numerical value ranging from 0 to 100 to indicate how fatigued the user is from physical activity occurring over the first period of time.
  • FIG. 13 a flow diagram of method 1300 for determining a third subscore (e.g., T score) of the fitness fatigue score is provided according to embodiments of the present disclosure.
  • the method 1300 can be implemented by, for instance, the system 900 discussed above with reference to FIG. 9. More particularly, one or more steps of the method 1000 can be performed by the processor 902 (FIG. 9) on the wearable computing device (e.g., smart watch 104 or 202). Alternatively, or additionally, one or more steps of the method 1000 can be performed by a computing device (e.g., host computer 922 of FIG. 9) that is remote relative to the smart watch.
  • FIG. 13 depicts steps performed in a particular order for purposes of illustration and discussion. Those of ordinary skill in the art, using the disclosures provided herein, will understand that various steps of the method 1300 may be adapted, modified, rearranged, performed simultaneously, or modified in various ways without deviating from the scope of the present disclosure.
  • the method 1300 can include determining a root mean square of successive differences (RMSSD) of heart rate variability measurements (HRV) for the user for each of a plurality of sleep events occurring over the third period of time.
  • RMSSD root mean square of successive differences
  • HRV heart rate variability measurements
  • the RMSSD of HRV measurements can be determined from biometric data (e.g., PPG signals) obtained from the one or more biometric sensors (e.g., PPG sensors) of the wearable computing device.
  • the method 1300 can include comparing the RMSSD of the user’s HRV during the user’s most recent sleep event during the third period of time to the RMSSD of HRV for at least one prior sleep event occurring during the third period of time.
  • the method 1300 can include determining the third subscore based, at least in part, on the comparison occurring at (1304).
  • the third subscore can be 0 when the RMSSD of the user’s HRV during the user’s most recent sleep event is lower than the RMSSD of the user’s HRV during one of the prior sleep events occurring during the third period of time.
  • the third subscore can be 100 when the RMSSD of the user’s HRV during the user’s most recent sleep event is higher than the RMSSD of the user’s HRV during one of the prior sleep events occurring during the third period of time.
  • the fitness fatigue score (e.g., daily readiness score) can be displayed on a display screen of the wearable computing device (e.g., smart watch 202 depicted in FIG. 2).
  • the fitness fatigue score can be a single numerical value. For instance, the fitness fatigue score of 98 for the current day can indicate the user is ready to engage in physical activity, such as a high-intensity workout. If the fitness fatigue score for the current day were lower (e.g., about 50 or about 20), the generated recommendation based on the fitness fatigue score would be different. For instance, the recommendation would be for the user to engage in a low-intensity workout or, alternatively, forego physical activity for the current day.
  • screen 1500 can indicate a daily readiness score (e.g., fitness fatigue score) for the user for the current day.
  • screen 1500 can illustrate the subscores of the daily readiness score as activity (e.g., first subscore), recent sleep (e.g., second subscore), and heart rate variability (e.g., third subscore).
  • Screen 1502 can include recommendation workouts for the user to try on the current day based on the user’s daily readiness score.
  • screen 1504 can illustrate the daily readiness scores determined for the user over the past week. In this manner, the user can see how their readiness score has varied over the past week.
  • wearable computing devices can generate and display a fitness fatigue score for the user for the current day. Furthermore, wearable computing devices can generate notifications regarding exercise for the user for the current day based, at least in part, on the fitness fatigue score for the user. In particular, wearable computing devices can generate a recommendation for the user to engage in a strenuous activity (e.g., running) when the fitness fatigue score indicates the user is well- rested. Conversely, wearable computing devices can generate a recommendation for the user to engage in a less strenuous activity (e.g., walking) or abstain from exercise when the fitness fatigue score is not well rested.
  • a strenuous activity e.g., running
  • wearable computing devices can generate a recommendation for the user to engage in a less strenuous activity (e.g., walking) or abstain from exercise when the fitness fatigue score is not well rested.
  • the fitness fatigue score is determined based on biometnc data collected through biometric sensors of the wearable computing device, the fitness fatigue score can be a better indicator of the user's current energy level than compared to the user’s own assessment of his or her energy levels. For example, instances can occur in which the user may feel ready to engage in the strenuous activity even though the user is actually fatigued and therefore not ready to engage in the strenuous activity. However, since the fitness fatigue score is determined based on biometric data and not how the user feels, the fitness fatigue score can provide a more objective indicator of the user’s readiness to engage in the strenuous activity.
  • wearable computing devices can provide recommendations regarding exercise based on an objective metric (e.g., fitness fatigue score) and can therefore reduce or eliminate instances in which the user feels ready to engage in the strenuous activity when the biometrics for the user indicate otherwise.
  • an objective metric e.g., fitness fatigue score
  • a user may be provided with controls allowing the user to make an election as to both if and when systems, programs, or features described herein may enable collection of user information (e.g., information about a user’s social network, social actions, or activities, profession, a user’s preferences, or a user’s current location), and if the user is sent content or communications from a server.
  • user information e.g., information about a user’s social network, social actions, or activities, profession, a user’s preferences, or a user’s current location
  • certain data may be treated in one or more ways before it is stored or used, so that personally identifiable information is removed.
  • a user’s identity may be treated so that no personally identifiable information can be determined for the user, or a user’s geographic location may be generalized where location information is obtained (such as to a city, ZIP code, or state level), so that a particular location of a user cannot be determined.
  • location information such as to a city, ZIP code, or state level
  • the user may have control over what information is collected about the user, how that information is used, and what information is provided to the user.
  • any information collected as described herein relating to the user will be kept private and confidential and will not be improperly used or published.

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Abstract

Un score de fatigue de condition physique pour un utilisateur pour un jour actuel est fourni. Le score de fatigue de condition physique peut être déterminé sur la base, au moins en partie, de premières données obtenues sur une première période de temps, de deuxièmes données obtenues sur une deuxième période de temps qui est plus courte en durée que la première période de temps, et de troisièmes données obtenues sur une troisième période de temps qui est plus longue en durée que la première période de temps. Les premières données comprennent des mesures de fréquence cardiaque pour l'utilisateur sur la première période de temps. Les secondes données comprennent une ou plusieurs métriques de sommeil pour une pluralité d'événements de sommeil pour l'utilisateur sur la seconde période de temps. Les troisièmes données comprennent une variabilité de fréquence cardiaque pour l'utilisateur sur la troisième période de temps. De plus, une recommandation concernant l'exercice pour le jour actuel peut être générée sur la base du score de fatigue de condition physique.
PCT/US2023/026837 2022-08-19 2023-07-03 Techniques de détermination et de gestion de score de fatigue de condition physique WO2024039450A1 (fr)

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Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20180116607A1 (en) * 2016-10-28 2018-05-03 Garmin Switzerland Gmbh Wearable monitoring device
US20190183412A1 (en) * 2016-08-08 2019-06-20 Koninklijke Philips N.V. System and method for assisting exercising of a subject
WO2022031671A1 (fr) * 2020-08-07 2022-02-10 Fitbit, Inc. Techniques de détermination et de gestion de stress

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20190183412A1 (en) * 2016-08-08 2019-06-20 Koninklijke Philips N.V. System and method for assisting exercising of a subject
US20180116607A1 (en) * 2016-10-28 2018-05-03 Garmin Switzerland Gmbh Wearable monitoring device
WO2022031671A1 (fr) * 2020-08-07 2022-02-10 Fitbit, Inc. Techniques de détermination et de gestion de stress

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