The following relates to wearable devices and data processing, including detecting epileptic seizures.
Some wearable devices may be configured to collect data from users associated with physiological events, such as neurological disorders. These wearable devices may collect physiological data, such as heart rate and motion of a user, enabling the wearable devices to sense a neurological disorder event based on the collected data.
A wearable device (e.g., a finger-worn ring device), may measure various physiological and non-physiological measurements of a user, such as heart rate, temperature, and motion, among other examples. The wearable device may communicate with a user device over a wireless connection. For example, the wearable device may communicate (e.g., receive, transmit, obtain, output) data to the user device over Bluetooth, Wi-Fi, or other wireless protocols. The user device may be configured with an application for receiving data from, or transmitting data to, the wearable device. Additionally, the application may be capable of, configured to, or operable to support processing (e.g., analyzing, decoding, encoding, etc.) the data for detecting epileptic seizure events.
An epileptic seizure event may be a sudden and uncontrolled burst of electrical activity in the brain of a user that leads to a range of symptoms and behaviors. Epileptic seizures events may vary in intensity and presentation, ranging from mild moments of changed consciousness or unusual sensations to severe convulsions and loss of awareness. Epileptic seizure events may be triggered by various factors, such as a user's stress level, a user's sleep pattern (e.g., sleep deprivation), etc. In some cases, detection of epileptic seizure events may be more challenging, such when a user is sleeping, or the like that may result in user fatality.
Various aspects of the present disclosure relate to enabling the wearable device and/or the user device to be capable of, configured to, or operable to support detecting an epileptic seizure event and alert a user, including family, caregivers, etc., of the detected epileptic seizure event. In some examples, the wearable device and/or the user device may be capable of, configured to, or operable to support detecting an imminent epileptic seizure event and alert the user prior to an occurrence of the epileptic seizure event. The user may wear the wearable device, such as a ring that may measure (e.g., sense) one or more physiological parameters of the user to determine abnormalities related to epileptic seizure events. For example, the wearable device may monitor an oxygen level associated with the user to detect breathing irregularities of the user, changes in a temperature of the user, or abnormal heart rhythms of the user.
The wearable device may output the measurements of the physiological parameters to the user device that may via the application be capable of, configured to, or operable to support a machine learning model for detecting an epileptic seizure event. The machine learning model may use these measurements, along with other information from various sources, such as user input, a health history of the user, a time of day, an electrodermal activity, etc., to detect the epileptic seizure event. The machine learning model may be capable of, configured to, or operable to support weighting various factors for detecting the epileptic seizure event. Upon detecting (e.g., determining) of the epileptic seizure, the machine learning model may output the result to the application. The user device may receive the result and alert the user or other personnel associated with the user (e.g., caregiver). The alert to the user may be an indication of the detected epileptic seizure event via the application of the user device.
Aspects of the disclosure are initially described in the context of systems supporting physiological data collection from users via wearable devices. Aspects of the disclosure are further illustrated by and described with reference to apparatus diagrams, system diagrams, a device diagram, and flowcharts that relate to detecting epileptic seizures.
The electronic devices may include any electronic devices known in the art, including wearable devices 104 (e.g., ring wearable devices, watch wearable devices, etc.), user devices 106 (e.g., smartphones, laptops, tablets). The electronic devices associated with the respective users 102 may include one or more of the following functionalities: 1) measuring physiological data, 2) storing the measured data, 3) processing the data, 4) providing outputs (e.g., via GUIs) to a user 102 based on the processed data, and 5) communicating data with one another and/or other computing devices. Different electronic devices may perform one or more of the functionalities.
Example wearable devices 104 may include wearable computing devices, such as a ring computing device (hereinafter “ring”) configured to be worn on a user's 102 finger, a wrist computing device (e.g., a smart watch, fitness band, or bracelet) configured to be worn on a user's 102 wrist, and/or a head mounted computing device (e.g., glasses/goggles). Wearable devices 104 may also include bands, straps (e.g., flexible or inflexible bands or straps), stick-on sensors, and the like, that may be positioned in other locations, such as bands around the head (e.g., a forehead headband), arm (e.g., a forearm band and/or bicep band), and/or leg (e.g., a thigh or calf band), behind the ear, under the armpit, and the like. Wearable devices 104 may also be attached to, or included in, articles of clothing. For example, wearable devices 104 may be included in pockets and/or pouches on clothing. As another example, wearable device 104 may be clipped and/or pinned to clothing, or may otherwise be maintained within the vicinity of the user 102. Example articles of clothing may include, but are not limited to, hats, shirts, gloves, pants, socks, outerwear (e.g., jackets), and undergarments. In some implementations, wearable devices 104 may be included with other types of devices such as training/sporting devices that are used during physical activity. For example, wearable devices 104 may be attached to, or included in, a bicycle, skis, a tennis racket, a golf club, and/or training weights.
Much of the present disclosure may be described in the context of a ring wearable device 104. Accordingly, the terms “ring 104,” “wearable device 104,” and like terms, may be used interchangeably, unless noted otherwise herein. However, the use of the term “ring 104” is not to be regarded as limiting, as it is contemplated herein that aspects of the present disclosure may be performed using other wearable devices (e.g., watch wearable devices, necklace wearable device, bracelet wearable devices, earring wearable devices, anklet wearable devices, and the like).
In some aspects, user devices 106 may include handheld mobile computing devices, such as smartphones and tablet computing devices. User devices 106 may also include personal computers, such as laptop and desktop computing devices. Other example user devices 106 may include server computing devices that may communicate with other electronic devices (e.g., via the Internet). In some implementations, computing devices may include medical devices, such as external wearable computing devices (e.g., Holter monitors). Medical devices may also include implantable medical devices, such as pacemakers and cardioverter defibrillators. Other example user devices 106 may include home computing devices, such as internet of things (IoT) devices (e.g., IoT devices), smart televisions, smart speakers, smart displays (e.g., video call displays), hubs (e.g., wireless communication hubs), security systems, smart appliances (e.g., thermostats and refrigerators), and fitness equipment.
Some electronic devices (e.g., wearable devices 104, user devices 106) may measure physiological parameters of respective users 102, such as photoplethysmography waveforms, continuous skin temperature, a pulse waveform, respiration rate, heart rate, heart rate variability (HRV), actigraphy, galvanic skin response, pulse oximetry, blood oxygen saturation (SpO2), blood sugar levels (e.g., glucose metrics), and/or other physiological parameters. Some electronic devices that measure physiological parameters may also perform some/all of the calculations described herein. Some electronic devices may not measure physiological parameters, but may perform some/all of the calculations described herein. For example, a ring (e.g., wearable device 104), mobile device application, or a server computing device may process received physiological data that was measured by other devices.
In some implementations, a user 102 may operate, or may be associated with, multiple electronic devices, some that may measure physiological parameters and some that may process the measured physiological parameters. In some implementations, a user 102 may have a ring (e.g., wearable device 104) that measures physiological parameters. The user 102 may also have, or be associated with, a user device 106 (e.g., mobile device, smartphone), where the wearable device 104 and the user device 106 are communicatively coupled to one another. In some cases, the user device 106 may receive data from the wearable device 104 and perform some/all of the calculations described herein. In some implementations, the user device 106 may also measure physiological parameters described herein, such as motion/activity parameters.
For example, as illustrated in
In some implementations, the rings 104 (e.g., wearable devices 104) of the system 100 may be configured to collect physiological data from the respective users 102 based on arterial blood flow within the user's finger. In particular, a ring 104 may utilize one or more light-emitting components, such as LEDs (e.g., red LEDs, green LEDs) that emit light on the palm-side of a user's finger to collect physiological data based on arterial blood flow within the user's finger. In general, the terms light-emitting components, light-emitting elements, and like terms, may include, but are not limited to, LEDs, micro LEDs, mini LEDs, laser diodes (LDs) (e.g., vertical cavity surface-emitting lasers (VCSELs), and the like.
In some cases, the system 100 may be configured to collect physiological data from the respective users 102 based on blood flow diffused into a microvascular bed of skin with capillaries and arterioles. For example, the system 100 may collect PPG data based on a measured amount of blood diffused into the microvascular system of capillaries and arterioles. In some implementations, the ring 104 may acquire the physiological data using a combination of both green and red LEDs. The physiological data may include any physiological data known in the art including, but not limited to, temperature data, accelerometer data (e.g., movement/motion data), heart rate data, HRV data, blood oxygen level data, or any combination thereof.
The use of both green and red LEDs may provide several advantages over other solutions, as red and green LEDs have been found to have their own distinct advantages when acquiring physiological data under different conditions (e.g., light/dark, active/inactive) and via different parts of the body, and the like. For example, green LEDs have been found to exhibit better performance during exercise. Moreover, using multiple LEDs (e.g., green and red LEDs) distributed around the ring 104 has been found to exhibit superior performance as compared to wearable devices that utilize LEDs that are positioned close to one another, such as within a watch wearable device. Furthermore, the blood vessels in the finger (e.g., arteries, capillaries) are more accessible via LEDs as compared to blood vessels in the wrist. In particular, arteries in the wrist are positioned on the bottom of the wrist (e.g., palm-side of the wrist), meaning only capillaries are accessible on the top of the wrist (e.g., back of hand side of the wrist), where wearable watch devices and similar devices are typically worn. As such, utilizing LEDs and other sensors within a ring 104 has been found to exhibit superior performance as compared to wearable devices worn on the wrist, as the ring 104 may have greater access to arteries (as compared to capillaries), thereby resulting in stronger signals and more valuable physiological data.
The electronic devices of the system 100 (e.g., user devices 106, wearable devices 104) may be communicatively coupled to one or more servers 110 via wired or wireless communication protocols. For example, as shown in
The system 100 may offer an on-demand database service between the user devices 106 and the one or more servers 110. In some cases, the servers 110 may receive data from the user devices 106 via the network 108, and may store and analyze the data. Similarly, the servers 110 may provide data to the user devices 106 via the network 108. In some cases, the servers 110 may be located at one or more data centers. The servers 110 may be used for data storage, management, and processing. In some implementations, the servers 110 may provide a web-based interface to the user device 106 via web browsers.
In some aspects, the system 100 may detect periods of time that a user 102 is asleep, and classify periods of time that the user 102 is asleep into one or more sleep stages (e.g., sleep stage classification). For example, as shown in
In some aspects, the system 100 may utilize circadian rhythm-derived features to further improve physiological data collection, data processing procedures, and other techniques described herein. The term circadian rhythm may refer to a natural, internal process that regulates an individual's sleep-wake cycle, that repeats approximately every 24 hours. In this regard, techniques described herein may utilize circadian rhythm adjustment models to improve physiological data collection, analysis, and data processing. For example, a circadian rhythm adjustment model may be input into a machine learning classifier along with physiological data collected from the user 102-a via the wearable device 104-a. In this example, the circadian rhythm adjustment model may be configured to “weight,” or adjust, physiological data collected throughout a user's natural, approximately 24-hour circadian rhythm. In some implementations, the system may initially start with a “baseline” circadian rhythm adjustment model, and may modify the baseline model using physiological data collected from each user 102 to generate tailored, individualized circadian rhythm adjustment models that are specific to each respective user 102.
In some aspects, the system 100 may utilize other biological rhythms to further improve physiological data collection, analysis, and processing by phase of these other rhythms. For example, if a weekly rhythm is detected within an individual's baseline data, then the model may be configured to adjust “weights” of data by day of the week. Biological rhythms that may require adjustment to the model by this method include: 1) ultradian (faster than a day rhythms, including sleep cycles in a sleep state, and oscillations from less than an hour to several hours periodicity in the measured physiological variables during wake state; 2) circadian rhythms; 3) non-endogenous daily rhythms shown to be imposed on top of circadian rhythms, as in work schedules; 4) weekly rhythms, or other artificial time periodicities exogenously imposed (e.g. in a hypothetical culture with 12 day “weeks,” 12 day rhythms could be used); 5) multi-day ovarian rhythms in women and spermatogenesis rhythms in men; 6) lunar rhythms (relevant for individuals living with low or no artificial lights); and 7) seasonal rhythms.
The biological rhythms are not always stationary rhythms. For example, many women experience variability in ovarian cycle length across cycles, and ultradian rhythms are not expected to occur at exactly the same time or periodicity across days even within a user 102. As such, signal processing techniques sufficient to quantify the frequency composition while preserving temporal resolution of these rhythms in physiological data may be used to improve detection of these rhythms, to assign phase of each rhythm to each moment in time measured, and to thereby modify adjustment models and comparisons of time intervals. The biological rhythm-adjustment models and parameters can be added in linear or non-linear combinations as appropriate to more accurately capture the dynamic physiological baselines of an individual or group of individuals.
In some aspects, the respective devices of the system 100 may support techniques for detecting epileptic seizures. A user device 106 may be capable of, configured to, or operable to activate an epileptic seizure mode associated with a wearable device 104 based on an activity a user 102 associated with the wearable device 104 is engaged in, at least one biometric associated with the user 102, a user selection to enable the epileptic seizure mode, or a combination thereof. The user device 106 may be capable of, configured to, or operable to receive physiological data measured from the user 102 by the wearable device 104 based on the enabled (e.g., activated) epileptic seizure mode. The physiological data measured from the user 102 by the wearable device 104 may include an oxygen saturation associated with the user 102, a heart rate associated with the user 102, a temperature associated with the user 102, an optical perfusion associated with the user 102, or a movement pattern associated with the user 102, or a combination thereof.
The user device 106 may be capable of, configured to, or operable to input the physiological data into a machine learning model configured to analyze the physiological data and identify an epileptic seizure event based on a relationship between the physiological data and a set of features. In some examples, the machine learning model may be a neural network that may be capable of, configured to, or operable to learn patterns and relationships in data through layers of interconnected nodes (e.g., between features of the set of features). In some other examples, the machine learning model may be a recurrent neural network (RNN) that may be capable of, configured to, or operable to learn patterns over time for identifying an epileptic seizure event. In other examples, the machine learning model may include convolutional neural networks (CNN), deep learning models, support vector machines (SVM), Gaussian mixture models (GMM), or Bayesian networks, etc.
The set of features may include activities associated with the user 102, biometrics associated with the user 102, or both. The activity may include a sleep activity or a physical activity. The at least one biometric may include an age of the user 102, a race of the user 102, an ethnicity of the user 102, a gender of the user 102, or a combination thereof. Additionally, or alternatively, the at least one biometric may include a health history of the user 102, and the health history of the user 102 may be indicative of epileptic seizures data related to prior epileptic seizure events associated with the user 102. The user device 106 may be capable of, configured to, or operable to obtain a result from the machine learning model indicating an occurrence of the epileptic seizure event, and output an indication of the epileptic seizure event based on the obtained result from the machine learning model. For example, the user device 106 may output the indication of the epileptic seizure event or cause the wearable device 104 to output the indication of the epileptic seizure event. Further details of the techniques are described herein with reference to at least
It should be appreciated by a person skilled in the art that one or more aspects of the disclosure may be implemented in a system 100 to additionally or alternatively solve other problems than those described above. Furthermore, aspects of the disclosure may provide technical improvements to “conventional” systems or processes as described herein. However, the description and appended drawings only include example technical improvements resulting from implementing aspects of the disclosure, and accordingly do not represent all of the technical improvements provided within the scope of the claims.
In some aspects, the ring 104 may be configured to be worn around a user's finger, and may determine one or more user physiological parameters when worn around the user's finger. Example measurements and determinations may include, but are not limited to, user skin temperature, pulse waveforms, respiratory rate, heart rate, HRV, blood oxygen levels (SpO2), blood sugar levels (e.g., glucose metrics), and the like.
The system 200 further includes a user device 106 (e.g., a smartphone) in communication with the ring 104. For example, the ring 104 may be in wireless and/or wired communication with the user device 106. In some implementations, the ring 104 may send measured and processed data (e.g., temperature data, photoplethysmogram (PPG) data, motion/accelerometer data, ring input data, and the like) to the user device 106. The user device 106 may also send data to the ring 104, such as ring 104 firmware/configuration updates. The user device 106 may process data. In some implementations, the user device 106 may transmit data to the server 110 for processing and/or storage.
The ring 104 may include a housing 205 that may include an inner housing 205-a and an outer housing 205-b. In some aspects, the housing 205 of the ring 104 may store or otherwise include various components of the ring including, but not limited to, device electronics, a power source (e.g., battery 210, and/or capacitor), one or more substrates (e.g., printable circuit boards) that interconnect the device electronics and/or power source, and the like. The device electronics may include device modules (e.g., hardware/software), such as: a processing module 230-a, a memory 215, a communication module 220-a, a power module 225, and the like. The device electronics may also include one or more sensors. Example sensors may include one or more temperature sensors 240, a PPG sensor assembly (e.g., PPG system 235), and one or more motion sensors 245.
The sensors may include associated modules (not illustrated) configured to communicate with the respective components/modules of the ring 104, and generate signals associated with the respective sensors. In some aspects, each of the components/modules of the ring 104 may be communicatively coupled to one another via wired or wireless connections. Moreover, the ring 104 may include additional and/or alternative sensors or other components that are configured to collect physiological data from the user, including light sensors (e.g., LEDs), oximeters, and the like.
The ring 104 shown and described with reference to
The housing 205 may include one or more housing 205 components. The housing 205 may include an outer housing 205-b component (e.g., a shell) and an inner housing 205-a component (e.g., a molding). The housing 205 may include additional components (e.g., additional layers) not explicitly illustrated in
The outer housing 205-b may be fabricated from one or more materials. In some implementations, the outer housing 205-b may include a metal, such as titanium, that may provide strength and abrasion resistance at a relatively light weight. The outer housing 205-b may also be fabricated from other materials, such polymers. In some implementations, the outer housing 205-b may be protective as well as decorative.
The inner housing 205-a may be configured to interface with the user's finger. The inner housing 205-a may be formed from a polymer (e.g., a medical grade polymer) or other material. In some implementations, the inner housing 205-a may be transparent. For example, the inner housing 205-a may be transparent to light emitted by the PPG light emitting diodes (LEDs). In some implementations, the inner housing 205-a component may be molded onto the outer housing 205-b. For example, the inner housing 205-a may include a polymer that is molded (e.g., injection molded) to fit into an outer housing 205-b metallic shell.
The ring 104 may include one or more substrates (not illustrated). The device electronics and battery 210 may be included on the one or more substrates. For example, the device electronics and battery 210 may be mounted on one or more substrates. Example substrates may include one or more printed circuit boards (PCBs), such as flexible PCB (e.g., polyimide). In some implementations, the electronics/battery 210 may include surface mounted devices (e.g., surface-mount technology (SMT) devices) on a flexible PCB. In some implementations, the one or more substrates (e.g., one or more flexible PCBs) may include electrical traces that provide electrical communication between device electronics. The electrical traces may also connect the battery 210 to the device electronics.
The device electronics, battery 210, and substrates may be arranged in the ring 104 in a variety of ways. In some implementations, one substrate that includes device electronics may be mounted along the bottom of the ring 104 (e.g., the bottom half), such that the sensors (e.g., PPG system 235, temperature sensors 240, motion sensors 245, and other sensors) interface with the underside of the user's finger. In these implementations, the battery 210 may be included along the top portion of the ring 104 (e.g., on another substrate).
The various components/modules of the ring 104 represent functionality (e.g., circuits and other components) that may be included in the ring 104. Modules may include any discrete and/or integrated electronic circuit components that implement analog and/or digital circuits capable of producing the functions attributed to the modules herein. For example, the modules may include analog circuits (e.g., amplification circuits, filtering circuits, analog/digital conversion circuits, and/or other signal conditioning circuits). The modules may also include digital circuits (e.g., combinational or sequential logic circuits, memory circuits etc.).
The memory 215 (memory module) of the ring 104 may include any volatile, non-volatile, magnetic, or electrical media, such as a random access memory (RAM), read-only memory (ROM), non-volatile RAM (NVRAM), electrically-erasable programmable ROM (EEPROM), flash memory, or any other memory device. The memory 215 may store any of the data described herein. For example, the memory 215 may be configured to store data (e.g., motion data, temperature data, PPG data) collected by the respective sensors and PPG system 235. Furthermore, memory 215 may include instructions that, when executed by one or more processing circuits, cause the modules to perform various functions attributed to the modules herein. The device electronics of the ring 104 described herein are only example device electronics. As such, the types of electronic components used to implement the device electronics may vary based on design considerations.
The functions attributed to the modules of the ring 104 described herein may be embodied as one or more processors, hardware, firmware, software, or any combination thereof. Depiction of different features as modules is intended to highlight different functional aspects and does not necessarily imply that such modules must be realized by separate hardware/software components. Rather, functionality associated with one or more modules may be performed by separate hardware/software components or integrated within common hardware/software components.
The processing module 230-a of the ring 104 may include one or more processors (e.g., processing units), microcontrollers, digital signal processors, systems on a chip (SOCs), and/or other processing devices. The processing module 230-a communicates with the modules included in the ring 104. For example, the processing module 230-a may transmit/receive data to/from the modules and other components of the ring 104, such as the sensors. As described herein, the modules may be implemented by various circuit components. Accordingly, the modules may also be referred to as circuits (e.g., a communication circuit and power circuit).
The processing module 230-a may communicate with the memory 215. The memory 215 may include computer-readable instructions that, when executed by the processing module 230-a, cause the processing module 230-a to perform the various functions attributed to the processing module 230-a herein. In some implementations, the processing module 230-a (e.g., a microcontroller) may include additional features associated with other modules, such as communication functionality provided by the communication module 220-a (e.g., an integrated Bluetooth Low Energy transceiver) and/or additional onboard memory 215.
The communication module 220-a may include circuits that provide wireless and/or wired communication with the user device 106 (e.g., communication module 220-b of the user device 106). In some implementations, the communication modules 220-a, 220-b may include wireless communication circuits, such as Bluetooth circuits and/or Wi-Fi circuits. In some implementations, the communication modules 220-a, 220-b can include wired communication circuits, such as Universal Serial Bus (USB) communication circuits. Using the communication module 220-a, the ring 104 and the user device 106 may be configured to communicate with each other. The processing module 230-a of the ring may be configured to transmit/receive data to/from the user device 106 via the communication module 220-a. Example data may include, but is not limited to, motion data, temperature data, pulse waveforms, heart rate data, HRV data, PPG data, and status updates (e.g., charging status, battery charge level, and/or ring 104 configuration settings). The processing module 230-a of the ring may also be configured to receive updates (e.g., software/firmware updates) and data from the user device 106.
The ring 104 may include a battery 210 (e.g., a rechargeable battery 210). An example battery 210 may include a Lithium-Ion or Lithium-Polymer type battery 210, although a variety of battery 210 options are possible. The battery 210 may be wirelessly charged. In some implementations, the ring 104 may include a power source other than the battery 210, such as a capacitor. The power source (e.g., battery 210 or capacitor) may have a curved geometry that matches the curve of the ring 104. In some aspects, a charger or other power source may include additional sensors that may be used to collect data in addition to, or that supplements, data collected by the ring 104 itself. Moreover, a charger or other power source for the ring 104 may function as a user device 106 and in this case the charger or other power source for the ring 104 may be configured to receive data from the ring 104, store and/or process data received from the ring 104, and communicate data between the ring 104 and the servers 110.
In some aspects, the ring 104 includes a power module 225 that may control charging of the battery 210. For example, the power module 225 may interface with an external wireless charger that charges the battery 210 when interfaced with the ring 104. The charger may include a datum structure that mates with a ring 104 datum structure to create a specified orientation with the ring 104 during charging. The power module 225 may also regulate voltage(s) of the device electronics, regulate power output to the device electronics, and monitor the state of charge of the battery 210. In some implementations, the battery 210 may include a protection circuit module (PCM) that protects the battery 210 from high current discharge, over voltage during charging, and under voltage during discharge. The power module 225 may also include electro-static discharge (ESD) protection.
The one or more temperature sensors 240 may be electrically coupled to the processing module 230-a. The temperature sensor 240 may be configured to generate a temperature signal (e.g., temperature data) that indicates a temperature read or sensed by the temperature sensor 240. The processing module 230-a may determine a temperature of the user in the location of the temperature sensor 240. For example, in the ring 104, temperature data generated by the temperature sensor 240 may indicate a temperature of a user at the user's finger (e.g., skin temperature). In some implementations, the temperature sensor 240 may contact the user's skin. In other implementations, a portion of the housing 205 (e.g., the inner housing 205-a) may form a barrier (e.g., a thin, thermally conductive barrier) between the temperature sensor 240 and the user's skin. In some implementations, portions of the ring 104 configured to contact the user's finger may have thermally conductive portions and thermally insulative portions. The thermally conductive portions may conduct heat from the user's finger to the temperature sensors 240. The thermally insulative portions may insulate portions of the ring 104 (e.g., the temperature sensor 240) from ambient temperature.
In some implementations, the temperature sensor 240 may generate a digital signal (e.g., temperature data) that the processing module 230-a may use to determine the temperature. As another example, in cases where the temperature sensor 240 includes a passive sensor, the processing module 230-a (or a temperature sensor 240 module) may measure a current/voltage generated by the temperature sensor 240 and determine the temperature based on the measured current/voltage. Example temperature sensors 240 may include a thermistor, such as a negative temperature coefficient (NTC) thermistor, or other types of sensors including resistors, transistors, diodes, and/or other electrical/electronic components.
The processing module 230-a may sample the user's temperature over time. For example, the processing module 230-a may sample the user's temperature according to a sampling rate. An example sampling rate may include one sample per second, although the processing module 230-a may be configured to sample the temperature signal at other sampling rates that are higher or lower than one sample per second. In some implementations, the processing module 230-a may sample the user's temperature continuously throughout the day and night. Sampling at a sufficient rate (e.g., one sample per second) throughout the day may provide sufficient temperature data for analysis described herein.
The processing module 230-a may store the sampled temperature data in memory 215. In some implementations, the processing module 230-a may process the sampled temperature data. For example, the processing module 230-a may determine average temperature values over a period of time. In one example, the processing module 230-a may determine an average temperature value each minute by summing all temperature values collected over the minute and dividing by the number of samples over the minute. In a specific example where the temperature is sampled at one sample per second, the average temperature may be a sum of all sampled temperatures for one minute divided by sixty seconds. The memory 215 may store the average temperature values over time. In some implementations, the memory 215 may store average temperatures (e.g., one per minute) instead of sampled temperatures in order to conserve memory 215.
The sampling rate may be stored in memory 215 and may be configurable. In some implementations, the sampling rate may be the same throughout the day and night. In other implementations, the sampling rate may be changed throughout the day/night. In some implementations, the ring 104 may filter/reject temperature readings, such as large spikes in temperature that are not indicative of physiological changes (e.g., a temperature spike from a hot shower). In some implementations, the ring 104 may filter/reject temperature readings that may not be reliable due to other factors, such as excessive motion during exercise (e.g., as indicated by a motion sensor 245).
The ring 104 (e.g., communication module) may transmit the sampled and/or average temperature data to the user device 106 for storage and/or further processing. The user device 106 may transfer the sampled and/or average temperature data to the server 110 for storage and/or further processing.
Although the ring 104 is illustrated as including a single temperature sensor 240, the ring 104 may include multiple temperature sensors 240 in one or more locations, such as arranged along the inner housing 205-a near the user's finger. In some implementations, the temperature sensors 240 may be stand-alone temperature sensors 240. Additionally, or alternatively, one or more temperature sensors 240 may be included with other components (e.g., packaged with other components), such as with the accelerometer and/or processor.
The processing module 230-a may acquire and process data from multiple temperature sensors 240 in a similar manner described with respect to a single temperature sensor 240. For example, the processing module 230 may individually sample, average, and store temperature data from each of the multiple temperature sensors 240. In other examples, the processing module 230-a may sample the sensors at different rates and average/store different values for the different sensors. In some implementations, the processing module 230-a may be configured to determine a single temperature based on the average of two or more temperatures determined by two or more temperature sensors 240 in different locations on the finger.
The temperature sensors 240 on the ring 104 may acquire distal temperatures at the user's finger (e.g., any finger). For example, one or more temperature sensors 240 on the ring 104 may acquire a user's temperature from the underside of a finger or at a different location on the finger. In some implementations, the ring 104 may continuously acquire distal temperature (e.g., at a sampling rate). Although distal temperature measured by a ring 104 at the finger is described herein, other devices may measure temperature at the same/different locations. In some cases, the distal temperature measured at a user's finger may differ from the temperature measured at a user's wrist or other external body location. Additionally, the distal temperature measured at a user's finger (e.g., a “shell” temperature) may differ from the user's core temperature. As such, the ring 104 may provide a useful temperature signal that may not be acquired at other internal/external locations of the body. In some cases, continuous temperature measurement at the finger may capture temperature fluctuations (e.g., small or large fluctuations) that may not be evident in core temperature. For example, continuous temperature measurement at the finger may capture minute-to-minute or hour-to-hour temperature fluctuations that provide additional insight that may not be provided by other temperature measurements elsewhere in the body.
The ring 104 may include a PPG system 235. The PPG system 235 may include one or more optical transmitters that transmit light. The PPG system 235 may also include one or more optical receivers that receive light transmitted by the one or more optical transmitters. An optical receiver may generate a signal (hereinafter “PPG” signal) that indicates an amount of light received by the optical receiver. The optical transmitters may illuminate a region of the user's finger. The PPG signal generated by the PPG system 235 may indicate the perfusion of blood in the illuminated region. For example, the PPG signal may indicate blood volume changes in the illuminated region caused by a user's pulse pressure. The processing module 230-a may sample the PPG signal and determine a user's pulse waveform based on the PPG signal. The processing module 230-a may determine a variety of physiological parameters based on the user's pulse waveform, such as a user's respiratory rate, heart rate, HRV, oxygen saturation, and other circulatory parameters.
In some implementations, the PPG system 235 may be configured as a reflective PPG system 235 where the optical receiver(s) receive transmitted light that is reflected through the region of the user's finger. In some implementations, the PPG system 235 may be configured as a transmissive PPG system 235 where the optical transmitter(s) and optical receiver(s) are arranged opposite to one another, such that light is transmitted directly through a portion of the user's finger to the optical receiver(s).
The number and ratio of transmitters and receivers included in the PPG system 235 may vary. Example optical transmitters may include light-emitting diodes (LEDs). The optical transmitters may transmit light in the infrared spectrum and/or other spectrums. Example optical receivers may include, but are not limited to, photosensors, phototransistors, and photodiodes. The optical receivers may be configured to generate PPG signals in response to the wavelengths received from the optical transmitters. The location of the transmitters and receivers may vary. Additionally, a single device may include reflective and/or transmissive PPG systems 235.
The PPG system 235 illustrated in
The processing module 230-a may control one or both of the optical transmitters to transmit light while sampling the PPG signal generated by the optical receiver. In some implementations, the processing module 230-a may cause the optical transmitter with the stronger received signal to transmit light while sampling the PPG signal generated by the optical receiver. For example, the selected optical transmitter may continuously emit light while the PPG signal is sampled at a sampling rate (e.g., 250 Hz).
Sampling the PPG signal generated by the PPG system 235 may result in a pulse waveform that may be referred to as a “PPG.” The pulse waveform may indicate blood pressure vs time for multiple cardiac cycles. The pulse waveform may include peaks that indicate cardiac cycles. Additionally, the pulse waveform may include respiratory induced variations that may be used to determine respiration rate. The processing module 230-a may store the pulse waveform in memory 215 in some implementations. The processing module 230-a may process the pulse waveform as it is generated and/or from memory 215 to determine user physiological parameters described herein.
The processing module 230-a may determine the user's heart rate based on the pulse waveform. For example, the processing module 230-a may determine heart rate (e.g., in beats per minute) based on the time between peaks in the pulse waveform. The time between peaks may be referred to as an interbeat interval (IBI). The processing module 230-a may store the determined heart rate values and IBI values in memory 215.
The processing module 230-a may determine HRV over time. For example, the processing module 230-a may determine HRV based on the variation in the IBIs. The processing module 230-a may store the HRV values over time in the memory 215. Moreover, the processing module 230-a may determine the user's respiratory rate over time. For example, the processing module 230-a may determine respiratory rate based on frequency modulation, amplitude modulation, or baseline modulation of the user's IBI values over a period of time. Respiratory rate may be calculated in breaths per minute or as another breathing rate (e.g., breaths per 30 seconds). The processing module 230-a may store user respiratory rate values over time in the memory 215.
The ring 104 may include one or more motion sensors 245, such as one or more accelerometers (e.g., 6-D accelerometers) and/or one or more gyroscopes (gyros). The motion sensors 245 may generate motion signals that indicate motion of the sensors. For example, the ring 104 may include one or more accelerometers that generate acceleration signals that indicate acceleration of the accelerometers. As another example, the ring 104 may include one or more gyro sensors that generate gyro signals that indicate angular motion (e.g., angular velocity) and/or changes in orientation. The motion sensors 245 may be included in one or more sensor packages. An example accelerometer/gyro sensor is a Bosch BMI160 inertial micro electro-mechanical system (MEMS) sensor that may measure angular rates and accelerations in three perpendicular axes.
The processing module 230-a may sample the motion signals at a sampling rate (e.g., 50 Hz) and determine the motion of the ring 104 based on the sampled motion signals. For example, the processing module 230-a may sample acceleration signals to determine acceleration of the ring 104. As another example, the processing module 230-a may sample a gyro signal to determine angular motion. In some implementations, the processing module 230-a may store motion data in memory 215. Motion data may include sampled motion data as well as motion data that is calculated based on the sampled motion signals (e.g., acceleration and angular values).
The ring 104 may store a variety of data described herein. For example, the ring 104 may store temperature data, such as raw sampled temperature data and calculated temperature data (e.g., average temperatures). As another example, the ring 104 may store PPG signal data, such as pulse waveforms and data calculated based on the pulse waveforms (e.g., heart rate values, IBI values, HRV values, and respiratory rate values). The ring 104 may also store motion data, such as sampled motion data that indicates linear and angular motion.
The ring 104, or other computing device, may calculate and store additional values based on the sampled/calculated physiological data. For example, the processing module 230 may calculate and store various metrics, such as sleep metrics (e.g., a Sleep Score), activity metrics, and readiness metrics. In some implementations, additional values/metrics may be referred to as “derived values.” The ring 104, or other computing/wearable device, may calculate a variety of values/metrics with respect to motion. Example derived values for motion data may include, but are not limited to, motion count values, regularity values, intensity values, metabolic equivalence of task values (METs), and orientation values. Motion counts, regularity values, intensity values, and METs may indicate an amount of user motion (e.g., velocity/acceleration) over time. Orientation values may indicate how the ring 104 is oriented on the user's finger and if the ring 104 is worn on the left hand or right hand.
In some implementations, motion counts and regularity values may be determined by counting a number of acceleration peaks within one or more periods of time (e.g., one or more 30 second to 1 minute periods). Intensity values may indicate a number of movements and the associated intensity (e.g., acceleration values) of the movements. The intensity values may be categorized as low, medium, and high, depending on associated threshold acceleration values. METs may be determined based on the intensity of movements during a period of time (e.g., 30 seconds), the regularity/irregularity of the movements, and the number of movements associated with the different intensities.
In some implementations, the processing module 230-a may compress the data stored in memory 215. For example, the processing module 230-a may delete sampled data after making calculations based on the sampled data. As another example, the processing module 230-a may average data over longer periods of time in order to reduce the number of stored values. In a specific example, if average temperatures for a user over one minute are stored in memory 215, the processing module 230-a may calculate average temperatures over a five minute time period for storage, and then subsequently erase the one minute average temperature data. The processing module 230-a may compress data based on a variety of factors, such as the total amount of used/available memory 215 and/or an elapsed time since the ring 104 last transmitted the data to the user device 106.
Although a user's physiological parameters may be measured by sensors included on a ring 104, other devices may measure a user's physiological parameters. For example, although a user's temperature may be measured by a temperature sensor 240 included in a ring 104, other devices may measure a user's temperature. In some examples, other wearable devices (e.g., wrist devices) may include sensors that measure user physiological parameters. Additionally, medical devices, such as external medical devices (e.g., wearable medical devices) and/or implantable medical devices, may measure a user's physiological parameters. One or more sensors on any type of computing device may be used to implement the techniques described herein.
The physiological measurements may be taken continuously throughout the day and/or night. In some implementations, the physiological measurements may be taken during portions of the day and/or portions of the night. In some implementations, the physiological measurements may be taken in response to determining that the user is in a specific state, such as an active state, resting state, and/or a sleeping state. For example, the ring 104 can make physiological measurements in a resting/sleep state in order to acquire cleaner physiological signals. In one example, the ring 104 or other device/system may detect when a user is resting and/or sleeping and acquire physiological parameters (e.g., temperature) for that detected state. The devices/systems may use the resting/sleep physiological data and/or other data when the user is in other states in order to implement the techniques of the present disclosure.
In some implementations, as described previously herein, the ring 104 may be configured to collect, store, and/or process data, and may transfer any of the data described herein to the user device 106 for storage and/or processing. In some aspects, the user device 106 includes a wearable application 250, an operating system (OS), a web browser application (e.g., web browser 280), one or more additional applications, and a GUI 275. The user device 106 may further include other modules and components, including sensors, audio devices, haptic feedback devices, and the like. The wearable application 250 may include an example of an application (e.g., “app”) that may be installed on the user device 106. The wearable application 250 may be configured to acquire data from the ring 104, store the acquired data, and process the acquired data as described herein. For example, the wearable application 250 may include a user interface (UI) module 255, an acquisition module 260, a processing module 230-b, a communication module 220-b, and a storage module (e.g., database 265) configured to store application data.
The various data processing operations described herein may be performed by the ring 104, the user device 106, the servers 110, or any combination thereof. For example, in some cases, data collected by the ring 104 may be pre-processed and transmitted to the user device 106. In this example, the user device 106 may perform some data processing operations on the received data, may transmit the data to the servers 110 for data processing, or both. For instance, in some cases, the user device 106 may perform processing operations that require relatively low processing power and/or operations that require a relatively low latency, whereas the user device 106 may transmit the data to the servers 110 for processing operations that require relatively high processing power and/or operations that may allow relatively higher latency.
In some aspects, the ring 104, user device 106, and server 110 of the system 200 may be configured to evaluate sleep patterns for a user. In particular, the respective components of the system 200 may be used to collect data from a user via the ring 104, and generate one or more scores (e.g., Sleep Score, Readiness Score) for the user based on the collected data. For example, as noted previously herein, the ring 104 of the system 200 may be worn by a user to collect data from the user, including temperature, heart rate, HRV, and the like. Data collected by the ring 104 may be used to determine when the user is asleep in order to evaluate the user's sleep for a given “sleep day.” In some aspects, scores may be calculated for the user for each respective sleep day, such that a first sleep day is associated with a first set of scores, and a second sleep day is associated with a second set of scores. Scores may be calculated for each respective sleep day based on data collected by the ring 104 during the respective sleep day. Scores may include, but are not limited to, Sleep Scores, Readiness Scores, and the like.
In some cases, “sleep days” may align with the traditional calendar days, such that a given sleep day runs from midnight to midnight of the respective calendar day. In other cases, sleep days may be offset relative to calendar days. For example, sleep days may run from 6:00 pm (18:00) of a calendar day until 6:00 pm (18:00) of the subsequent calendar day. In this example, 6:00 pm may serve as a “cut-off time,” where data collected from the user before 6:00 pm is counted for the current sleep day, and data collected from the user after 6:00 pm is counted for the subsequent sleep day. Due to the fact that most individuals sleep the most at night, offsetting sleep days relative to calendar days may enable the system 200 to evaluate sleep patterns for users in such a manner that is consistent with their sleep schedules. In some cases, users may be able to selectively adjust (e.g., via the GUI) a timing of sleep days relative to calendar days so that the sleep days are aligned with the duration of time that the respective users typically sleep.
In some implementations, each overall score for a user for each respective day (e.g., Sleep Score, Readiness Score) may be determined/calculated based on one or more “contributors,” “factors,” or “contributing factors.” For example, a user's overall Sleep Score may be calculated based on a set of contributors, including: total sleep, efficiency, restfulness, REM sleep, deep sleep, latency, timing, or any combination thereof. The Sleep Score may include any quantity of contributors. The “total sleep” contributor may refer to the sum of all sleep periods of the sleep day. The “efficiency” contributor may reflect the percentage of time spent asleep compared to time spent awake while in bed, and may be calculated using the efficiency average of long sleep periods (e.g., primary sleep period) of the sleep day, weighted by a duration of each sleep period. The “restfulness” contributor may indicate how restful the user's sleep is, and may be calculated using the average of all sleep periods of the sleep day, weighted by a duration of each period. The restfulness contributor may be based on a “wake up count” (e.g., sum of all the wake-ups (when user wakes up) detected during different sleep periods), excessive movement, and a “got up count” (e.g., sum of all the got-ups (when user gets out of bed) detected during the different sleep periods).
The “REM sleep” contributor may refer to a sum total of REM sleep durations across all sleep periods of the sleep day including REM sleep. Similarly, the “deep sleep” contributor may refer to a sum total of deep sleep durations across all sleep periods of the sleep day including deep sleep. The “latency” contributor may signify how long (e.g., average, median, longest) the user takes to go to sleep, and may be calculated using the average of long sleep periods throughout the sleep day, weighted by a duration of each period and the number of such periods (e.g., consolidation of a given sleep stage or sleep stages may be its own contributor or weight other contributors). Lastly, the “timing” contributor may refer to a relative timing of sleep periods within the sleep day and/or calendar day, and may be calculated using the average of all sleep periods of the sleep day, weighted by a duration of each period.
By way of another example, a user's overall Readiness Score may be calculated based on a set of contributors, including: sleep, sleep balance, heart rate, HRV balance, recovery index, temperature, activity, activity balance, or any combination thereof. The Readiness Score may include any quantity of contributors. The “sleep” contributor may refer to the combined Sleep Score of all sleep periods within the sleep day. The “sleep balance” contributor may refer to a cumulative duration of all sleep periods within the sleep day. In particular, sleep balance may indicate to a user whether the sleep that the user has been getting over some duration of time (e.g., the past two weeks) is in balance with the user's needs. Typically, adults need 7-9 hours of sleep a night to stay healthy, alert, and to perform at their best both mentally and physically. However, it is normal to have an occasional night of bad sleep, so the sleep balance contributor takes into account long-term sleep patterns to determine whether each user's sleep needs are being met. The “resting heart rate” contributor may indicate a lowest heart rate from the longest sleep period of the sleep day (e.g., primary sleep period) and/or the lowest heart rate from naps occurring after the primary sleep period.
Continuing with reference to the “contributors” (e.g., factors, contributing factors) of the Readiness Score, the “HRV balance” contributor may indicate a highest HRV average from the primary sleep period and the naps happening after the primary sleep period. The HRV balance contributor may help users keep track of their recovery status by comparing their HRV trend over a first time period (e.g., two weeks) to an average HRV over some second, longer time period (e.g., three months). The “recovery index” contributor may be calculated based on the longest sleep period. Recovery index measures how long it takes for a user's resting heart rate to stabilize during the night. A sign of a very good recovery is that the user's resting heart rate stabilizes during the first half of the night, at least six hours before the user wakes up, leaving the body time to recover for the next day. The “body temperature” contributor may be calculated based on the longest sleep period (e.g., primary sleep period) or based on a nap happening after the longest sleep period if the user's highest temperature during the nap is at least 0.5° C. higher than the highest temperature during the longest period. In some aspects, the ring may measure a user's body temperature while the user is asleep, and the system 200 may display the user's average temperature relative to the user's baseline temperature. If a user's body temperature is outside of their normal range (e.g., clearly above or below 0.0), the body temperature contributor may be highlighted (e.g., go to a “Pay attention” state) or otherwise generate an alert for the user.
In some aspects, the system 200 may support techniques for detecting epileptic seizures. A user device 106 may be capable of, configured to, or operable to activate an epileptic seizure mode associated with a ring 104 based on an activity a user associated with the ring 104 is engaged in, at least one biometric associated with the user 102, a user selection to enable the epileptic seizure mode, or a combination thereof. The user device 106 may be capable of, configured to, or operable to receive physiological data measured from the user by the ring 104 based on the enabled epileptic seizure mode. The epileptic seizure mode may be enabled by the user via the user device 106. By enabling the epileptic seizure mode, the user device 106 and the ring 104 may exchange data (e.g., physiological data measured from the user by the ring 104) at a higher frequency (e.g., periodicity) compared to when the epileptic seizure mode is disabled (e.g., deactivated).
The user device 106 may be capable of, configured to, or operable to input the physiological data into a machine learning model configured to analyze the physiological data and identify an epileptic seizure event based on a relationship between the physiological data and a set of features. The user device 106 may be capable of, configured to, or operable to obtain a result from the machine learning model indicating an occurrence of the epileptic seizure event, and output an indication of the epileptic seizure event based on the obtained result from the machine learning model. For example, the user device 106 may output the indication of the epileptic seizure event or cause the ring 104 to output the indication of the epileptic seizure event. In some examples, the output of the indication of the epileptic seizure event may be a predicted seizure event, such as a notification that a seizure event is likely to occur in the near future. In some examples, the user device 106 may disable the epileptic seizure mode associated with the ring 104 in response to detecting the epileptic seizure event or after an expiration of a timer. The user device 106 may activate the timer in response to detecting the epileptic seizure event, and after the timer lapses, the user device 106 may disable the epileptic seizure mode associated with the ring 104 and return to a default mode. Further details of the techniques are described herein with reference to at least
The user device 306 may be capable of, configured to, or operable to support an interface 307 for outputting and inputting information related to epileptic seizure events. In some examples, the user device 306 may activate an epileptic seizure mode 315 associated with the wearable device 304 based on an activity a user associated with the wearable device 304 is engaged in, at least one biometric associated with the user, or a user selection to enable the epileptic seizure mode 315, or a combination thereof. Examples of activities the user may be engaged in include a sleep activity and/or a physical activity. In some cases, the user may be more likely to experience an epileptic seizure event when sleeping, and as such the epileptic seizure mode 315 may be activated prior to the user being asleep or while the user is asleep (e.g., the user device 306 may determine that the user is asleep based on sensor data obtained from the wearable device 304). Examples of biometrics associated with the user may include a health history of the user, such as a health history indicating epileptic seizure data related to prior epileptic seizure events associated with the user. For example, if a biometric of the user, such as the health history of the user, indicates that the user is known to experience epileptic seizure events during a specific time of day, the epileptic seizure mode 315 may be activated during the same time of day or a predetermined period prior to the time of day the user may experience epileptic seizure events. It should be understood that the epileptic seizure mode 315 may be activated based on various factors, such as the user engaging in a sleep activity and the age of the user, among other combinations. In some examples, the epileptic seizure mode 315 may be activated by another device, such as the wearable device 304 or a server (e.g., an application server).
The wearable device 304 and/or the user device 306 may be configured with a receiver, a transmitter, or both, for receiving and/or transmitting information such as packets, data, control information, or any combination thereof associated with various information channels. In response to the activation of the epileptic seizure mode 315, the wearable device 304 may be capable of, configured to, or operable to support measuring physiological data from a user in accordance with the activated epileptic seizure mode 315. For example, the wearable device 304 may measure an oxygen saturation associated with the user, a heart rate associated with the user, a temperature associated with the user, an optical perfusion associated with the user, or a movement pattern associated with the user, or a combination thereof, in accordance with a periodicity configured by the activated epileptic seizure mode 315. The wearable device 304 may transmit, and the user device 306 may receive, the physiological data measured (e.g., measurements 310) from the user by the wearable device over a channel 305. The channel 305 may be associated with a wireless protocol, such as Bluetooth, Wi-Fi, or other wireless protocols.
The wearable device 304 may transmit, and the user device 306 may receive, the physiological data measured (e.g., measurements 310) from the user by the wearable device according to a periodicity configured by the activated epileptic seizure mode 315. For example, the wearable device 304 may transmit, and the user device 306 may receive, the physiological data measured (e.g., measurements 310) from the user by the wearable device, every 3 milliseconds. When the epileptic seizure mode 315 is disabled (e.g., deactivated), the periodicity may be longer than when the epileptic seizure mode 315 is enabled (e.g., activated), such as every 5 milliseconds.
In some examples, oxygen saturation associated with the user may include a baseline oxygen saturation (e.g., a resting oxygen saturation level of 98%) associated with the user, a post-exercise oxygen saturation (e.g., an oxygen saturation dropped to 94% after a workout) associated with the user, a sleeping oxygen saturation (e.g., an averaged 96% oxygen saturation during sleep) associated with the user, an oxygen saturation fluctuation (e.g., ranged between 96% and 98% during daily activities by the user) associated with the user, etc. In some examples, heart rate associated with the user may include a resting heart rate associated with the user (e.g., a resting heart rate of 60 beats per minute (bpm)), an exercise heart rate associated with the user (e.g., during a workout, the user's heart rate reached 150 bpm), a sleeping heart rate associated with the user (e.g., averaged 52 bpm heart rate during sleep), etc.
In some examples, temperature associated with the user may include a body temperature associated with the user (e.g., 98.6° F. (37° C.)), a baseline temperature associated with the user (e.g., an average temperature of 98.0° F.), a temperature drop associated with the user (e.g., the temperature decreased from 99.5° F. to 97.9° F.), a nighttime temperature associated with the user (e.g., a body temperature registered at 98.9° F. prior to bedtime), a post-exercise temperature associated with the user (e.g., a temperature of 99.3° F. after a workout), a sleep temperature associated with the user during sleep (e.g., a temperature averaged 97.7° F. while the user is asleep), etc.
In some examples, optical perfusion associated with the user may include muscle oxygenation associated with the user (e.g., measurements of oxygen levels in muscles during an activity of the user, such as sleep or exercise to assess perfusion and fatigue), tissue viability associated with the user (e.g., measurements of blood flow in an area of the user to determine tissue health), skin perfusion associated with the user (e.g., measurements of blood flow in the skin of the user to monitor circulatory conditions), etc. In some examples, movement pattern associated with the user may include walking, running, cycling, sitting, standing, rolling, kicking, crawling, rowing, and the like.
The user device 306 may input the measurements 310 (e.g., physiological data measured by the wearable device 304) into a machine learning model 320 that may be configured to analyze the physiological data and identify an epileptic seizure event based on a relationship between the physiological data and a set of features. The set of features may include activities 323 associated with the user, biometrics 321 associated with the user, or both. The machine learning model 320 may be configured to analyze the measurements 310 and identify an epileptic seizure event 325 based on a relationship between the measurements 310 and the set of features (e.g., activities 323 and biometrics 321). The machine learning model 320 may include a neural network learning model, a decision tree learning model, a SVM learning model, or a combination thereof.
The user device 306 may be capable of, configured to, or operable to support the machine learning model 320. For example, the user device 306 may include instructions that, when executed by the user device 306, cause the user device 306 to perform various functions of the machine learning model 320. In some other examples, the various functions of the machine learning model 320 may be performed partially at the user device 306. In other examples, the various functions of the machine learning model 320 may be performed remote from the user device. For example, aspects of the machine learning model 320 may be supported by a cloud platform application. This may enable the user device 306 to experience reduced power consumption by moving the processing of the measurements 310 for detecting epileptic seizure events to the cloud (e.g., a network of one or more remote servers hosted on the Internet to store, manage, and process data instead of using a local server or the user device 306).
The machine learning model 320 may output a result, indicating the identification of the epileptic seizure event 325. In some examples, the result may be identification of an upcoming epileptic seizure event 325 or predicted epileptic seizure event 325. The result may be received (e.g., obtained) by the user device 306, and the user device 306 may output an indication of the identified epileptic seizure event 325 based on the obtained result from the machine learning model 320. For example, the user device 306 may output an indication, such as a text message, to a user via the interface 307. In some examples, the epileptic seizure event 325 may be obtained and outputted by the wearable device 304, or another device. The indication of the epileptic seizure event 325 may be a haptic output, a message output, or any combination thereof. For example, the user device 306 may vibrate and display a text message. In some examples, the wearable device 304 may vibrate, display an LED light, or both.
In some examples, the machine learning model 320 may identify the epileptic seizure event 325 within a threshold period of time of seizure onset for the user based on the relationship between the measurements 310 and the set of features (e.g., activities 323 and biometrics 321). For example, for timely and effective seizure identification for the user, the epileptic seizure event 325 may be identified within seconds of seizure onset. In some examples, the machine learning model 320 may identify or predict a future epileptic seizure event 325, and many notify the user prior to seizure onset. In such examples, the user may have time to react, such as by calling for help or taking other appropriate measures.
The machine learning model 320 may apply one or more weights to the measurements 310 and the set of features based on the activity the user is engaged in, one or more biometrics of the user, or both. The result from the machine learning model 320, the epileptic seizure event 325, may be based on applying the one or more weights. For example, heart rate may be applied a greater weight than age. In some other examples, if a user experiences increased temperature as indicated by the biometrics 321 when experiencing an epileptic seizure, the machine learning model 320 may apply greater weight to the measurements 310 from the wearable device 304.
The notification 405 may include one or more features, such as sound, haptics (e.g., vibrations), text, and visuals. For example, the notification 405 may present a message such as, “You have experienced an epileptic seizure. Here is some insight into your unique biometrics. Your seizure lasted one minute. Your heart rate had a maximum of 180.” The notification 405 may notify a user associated with the user device 406 of the epileptic seizure event, as well as biometrics specific to the user prior to, during, and/or after the epileptic seizure event. For example, the notification 405 may display biometrics, such as heart rate prior to, during, and/or after the epileptic seizure event. In some examples, if the heart rate associated with the user increases with an epileptic seizure event, the user may be shown heart rate data as simple graphs describing the user's heart rate before, during, and after the epileptic seizure event.
The input module 510 may provide a means for receiving information such as packets, user data, control information, or any combination thereof associated with various information channels (e.g., control channels, data channels, information channels related to illness detection techniques). Information may be passed on to other components of the device 505. The input module 510 may utilize a single antenna or a set of multiple antennas.
The output module 515 may provide a means for transmitting signals generated by other components of the device 505. For example, the output module 515 may transmit information such as packets, user data, control information, or any combination thereof associated with various information channels (e.g., control channels, data channels, information channels related to illness detection techniques). In some examples, the output module 515 may be co-located with the input module 510 in a transceiver module. The output module 515 may utilize a single antenna or a set of multiple antennas.
For example, the wearable application 520 may include a physiological data reception component 525, a machine learning model component 530, a machine learning model result component 535, an indication component 540, or any combination thereof. In some examples, the wearable application 520, or various components thereof, may be configured to perform various operations (e.g., receiving, monitoring, transmitting) using or otherwise in cooperation with the input module 510, the output module 515, or both. For example, the wearable application 520 may receive information from the input module 510, send information to the output module 515, or be integrated in combination with the input module 510, the output module 515, or both to receive information, transmit information, or perform various other operations as described herein.
The physiological data reception component 525 may be configured as or otherwise support a means for receiving physiological data measured from a user by a wearable device. The machine learning model component 530 may be configured as or otherwise support a means for inputting the physiological data into a machine learning model configured to analyze the physiological data and identify an epileptic seizure event based at least in part on a relationship between the physiological data and a set of features, wherein the set of features comprises activities associated with the user, biometrics associated with the user, or both. The machine learning model result component 535 may be configured as or otherwise support a means for obtaining a result from the machine learning model indicating an occurrence of the epileptic seizure event. The indication component 540 may be configured as or otherwise support a means for outputting an indication of the epileptic seizure event based at least in part on the obtained result from the machine learning model.
The wearable application 620 may support detecting epileptic seizures in accordance with examples as disclosed herein. The physiological data reception component 630 may be configured as or otherwise support a means for receiving physiological data measured from a user by a wearable device. The machine learning model component 635 may be configured as or otherwise support a means for inputting the physiological data into a machine learning model configured to analyze the physiological data and identify an epileptic seizure event based at least in part on a relationship between the physiological data and a set of features, wherein the set of features comprises activities associated with the user, biometrics associated with the user, or both. The machine learning model result component 640 may be configured as or otherwise support a means for obtaining a result from the machine learning model indicating an occurrence of the epileptic seizure event. The indication component 645 may be configured as or otherwise support a means for outputting an indication of the epileptic seizure event based at least in part on the obtained result from the machine learning model.
The epileptic seizure mode activation component 625 may be configured as or otherwise support a means for activating an epileptic seizure mode associated with the wearable device based at least in part on an activity the user associated with the wearable device is engaged in, at least one biometric associated with the user, a user selection to enable the epileptic seizure mode, or a combination thereof. In some examples, the physiological data reception component 630 may be configured as or otherwise support a means for receiving physiological data based at least in part on the activated epileptic seizure mode.
In some examples, the physiological data reception component 630 may be configured as or otherwise support a means for receiving the physiological data measured from the user by the wearable device is based at least in part on a first periodicity. In some examples, the first periodicity is based at least in part on the epileptic seizure mode being activated.
In some examples, the first periodicity associated with the epileptic seizure mode being activated is greater than a second periodicity associated with the epileptic seizure mode being deactivated.
In some examples, the activity comprises a sleep activity, a physical activity, or both.
In some examples, the at least one biometric comprises an age of the user, a race of the user, an ethnicity of the user, a gender of the user, or a combination thereof. In some examples, the at least one biometric comprises a health history of the user. In some examples, the health history of the user indicates epileptic seizures data related to prior epileptic seizure events associated with the user.
In some examples, the machine learning model component 635 may be configured as or otherwise support a means for causing the wearable device to output the indication of the epileptic seizure event based at least in part on the obtained result from the machine learning model.
In some examples, the machine learning model component 635 may be configured as or otherwise support a means for causing a user device associated with the wearable device to output the indication of the epileptic seizure event based at least in part on the obtained result from the machine learning model.
In some examples, the machine learning model component 635 may be configured as or otherwise support a means for enabling the machine learning model to identify the epileptic seizure event within a threshold period of time of seizure onset for the user based at least in part on the relationship between the physiological data and the set of features.
In some examples, the machine learning model component 635 may be configured as or otherwise support a means for applying one or more weights to the physiological data and the set of features based at least in part on the activity the user associated with the wearable device is engaged in, the at least one biometric associated with the user, or both. In some examples, the machine learning model component 635 may be configured as or otherwise support a means for obtaining the result from the machine learning model indicating the occurrence of the epileptic seizure event based at least in part on applying the one or more weights to the physiological data and the set of features.
In some examples, the physiological data comprises one or more of an oxygen saturation associated with the user, a heart rate associated with the user, a temperature associated with the user, an optical perfusion associated with the user, or a movement pattern associated with the user.
In some examples, the machine learning model comprises a neural network learning model, a decision tree learning model, a support vector machine learning model, or a combination thereof.
In some examples, the indication of the epileptic seizure event comprises an audio output, a haptic output, a message output, or any combination thereof.
The communication module 710 may manage input and output signals for the device 705 via the antenna 715. The communication module 710 may include an example of the communication module 220-b of the user device 106 shown and described in
In some cases, the device 705 may include a single antenna 715. However, in some other cases, the device 705 may have more than one antenna 715 that may be capable of concurrently transmitting or receiving multiple wireless transmissions. The communication module 710 may communicate bi-directionally, via the one or more antennas 715, wired, or wireless links as described herein. For example, the communication module 710 may represent a wireless transceiver and may communicate bi-directionally with another wireless transceiver. The communication module 710 may also include a modem to modulate the packets, to provide the modulated packets to one or more antennas 715 for transmission, and to demodulate packets received from the one or more antennas 715.
The user interface component 725 may manage data storage and processing in a database 730. In some cases, a user may interact with the user interface component 725. In other cases, the user interface component 725 may operate automatically without user interaction. The database 730 may be an example of a single database, a distributed database, multiple distributed databases, a data store, a data lake, or an emergency backup database.
The memory 735 may include RAM and ROM. The memory 735 may store computer-readable, computer-executable software including instructions that, when executed, cause the processor 740 to perform various functions described herein. In some cases, the memory 735 may contain, among other things, a BIOS that may control basic hardware or software operation such as the interaction with peripheral components or devices.
The processor 740 may include an intelligent hardware device, (e.g., a general-purpose processor, a DSP, a CPU, a microcontroller, an ASIC, an FPGA, a programmable logic device, a discrete gate or transistor logic component, a discrete hardware component, or any combination thereof). In some cases, the processor 740 may be configured to operate a memory array using a memory controller. In other cases, a memory controller may be integrated into the processor 740. The processor 740 may be configured to execute computer-readable instructions stored in a memory 735 to perform various functions (e.g., functions or tasks supporting a method and system for sleep staging algorithms).
The wearable application 720 may support detecting epileptic seizures in accordance with examples as disclosed herein. For example, the wearable application 720 may be configured as or otherwise support a means for receiving physiological data measured from a user by a wearable device. The wearable application 720 may be configured as or otherwise support a means for inputting the physiological data into a machine learning model configured to analyze the physiological data and identify an epileptic seizure event based at least in part on a relationship between the physiological data and a set of features, wherein the set of features comprises activities associated with the user, biometrics associated with the user, or both. The wearable application 720 may be configured as or otherwise support a means for obtaining a result from the machine learning model indicating an occurrence of the epileptic seizure event. The wearable application 720 may be configured as or otherwise support a means for outputting an indication of the epileptic seizure event based at least in part on the obtained result from the machine learning model.
By including or configuring the wearable application 720 in accordance with examples as described herein, the device 705 may support techniques for reduced power consumption and improved utilization of processing capability.
The wearable application 720 may include an application (e.g., “app”), program, software, or other component that is configured to facilitate communications with a ring 104, server 110, other user devices 106, and the like. For example, the wearable application 720 may include an application executable on a user device 106 that is configured to receive data (e.g., physiological data) from a ring 104, perform processing operations on the received data, transmit and receive data with the servers 110, and cause presentation of data to a user 102.
At 805, the method may include receiving physiological data measured from a user by a wearable device. The operations of block 805 may be performed in accordance with examples as disclosed herein. In some examples, aspects of the operations of 805 may be performed by a physiological data reception component 630 as described with reference to
At 810, the method may include inputting the physiological data into a machine learning model configured to analyze the physiological data and identify an epileptic seizure event based at least in part on a relationship between the physiological data and a set of features, wherein the set of features comprises activities associated with the user, biometrics associated with the user, or both. The operations of block 810 may be performed in accordance with examples as disclosed herein. In some examples, aspects of the operations of 810 may be performed by a machine learning model component 635 as described with reference to
At 815, the method may include obtaining a result from the machine learning model indicating an occurrence of the epileptic seizure event. The operations of block 815 may be performed in accordance with examples as disclosed herein. In some examples, aspects of the operations of 815 may be performed by a machine learning model result component 640 as described with reference to
At 820, the method may include outputting an indication of the epileptic seizure event based at least in part on the obtained result from the machine learning model. The operations of block 820 may be performed in accordance with examples as disclosed herein. In some examples, aspects of the operations of 820 may be performed by an indication component 645 as described with reference to
It should be noted that the methods described above describe possible implementations, and that the operations and the steps may be rearranged or otherwise modified and that other implementations are possible. Furthermore, aspects from two or more of the methods may be combined.
A method for detecting epileptic seizures by an apparatus is described. The method may include receiving physiological data measured from a user by a wearable device, inputting the physiological data into a machine learning model configured to analyze the physiological data and identify an epileptic seizure event based at least in part on a relationship between the physiological data and a set of features, wherein the set of features comprises activities associated with the user, biometrics associated with the user, or both, obtaining a result from the machine learning model indicating an occurrence of the epileptic seizure event, and outputting an indication of the epileptic seizure event based at least in part on the obtained result from the machine learning model.
An apparatus for detecting epileptic seizures is described. The apparatus may include one or more memories storing processor executable code, and one or more processors coupled with the one or more memories. The one or more processors may individually or collectively operable to execute the code to cause the apparatus to receive physiological data measured from a user by a wearable device, input the physiological data into a machine learning model configured to analyze the physiological data and identify an epileptic seizure event based at least in part on a relationship between the physiological data and a set of features, wherein the set of features comprises activities associated with the user, biometrics associated with the user, or both, obtain a result from the machine learning model indicating an occurrence of the epileptic seizure event, and output an indication of the epileptic seizure event based at least in part on the obtained result from the machine learning model.
Another apparatus for detecting epileptic seizures is described. The apparatus may include means for receiving physiological data measured from a user by a wearable device, means for inputting the physiological data into a machine learning model configured to analyze the physiological data and identify an epileptic seizure event based at least in part on a relationship between the physiological data and a set of features, wherein the set of features comprises activities associated with the user, biometrics associated with the user, or both, means for obtaining a result from the machine learning model indicating an occurrence of the epileptic seizure event, and means for outputting an indication of the epileptic seizure event based at least in part on the obtained result from the machine learning model.
A non-transitory computer-readable medium storing code for detecting epileptic seizures is described. The code may include instructions executable by a processor to receive physiological data measured from a user by a wearable device, input the physiological data into a machine learning model configured to analyze the physiological data and identify an epileptic seizure event based at least in part on a relationship between the physiological data and a set of features, wherein the set of features comprises activities associated with the user, biometrics associated with the user, or both, obtain a result from the machine learning model indicating an occurrence of the epileptic seizure event, and output an indication of the epileptic seizure event based at least in part on the obtained result from the machine learning model.
Some examples of the method, apparatus, and non-transitory computer-readable medium described herein may further include operations, features, means, or instructions for causing the wearable device to activate an epileptic seizure mode associated with the wearable device based at least in part on an activity the user associated with the wearable device is engaged in, at least one biometric associated with the user, a user selection to activate the epileptic seizure mode, or a combination thereof, wherein receiving the physiological data is based at least in part on the activated epileptic seizure mode.
Some examples of the method, apparatus, and non-transitory computer-readable medium described herein may further include operations, features, means, or instructions for receiving the physiological data measured from the user by the wearable device may be based at least in part on a first periodicity and the first periodicity may be based at least in part on the epileptic seizure mode being activated.
In some examples of the method, apparatus, and non-transitory computer-readable medium described herein, the first periodicity associated with the epileptic seizure mode being activated may be greater than a second periodicity associated with the epileptic seizure mode being deactivated.
In some examples of the method, apparatus, and non-transitory computer-readable medium described herein, the activity comprises a sleep activity, a physical activity, or both.
In some examples of the method, apparatus, and non-transitory computer-readable medium described herein, the at least one biometric comprises an age of the user, a race of the user, an ethnicity of the user, a gender of the user, the health history of the user or a combination thereof, and wherein the health history of the user indicates epileptic seizures data related to prior epileptic seizure events associated with the user.
Some examples of the method, apparatus, and non-transitory computer-readable medium described herein may further include operations, features, means, or instructions for causing the wearable device to output the indication of the epileptic seizure event based at least in part on the obtained result from the machine learning model.
Some examples of the method, apparatus, and non-transitory computer-readable medium described herein may further include operations, features, means, or instructions for causing a user device associated with the wearable device to output the indication of the epileptic seizure event based at least in part on the obtained result from the machine learning model.
Some examples of the method, apparatus, and non-transitory computer-readable medium described herein may further include operations, features, means, or instructions for enabling the machine learning model to identify the epileptic seizure event within a threshold period of time of seizure onset for the user based at least in part on the relationship between the physiological data and the set of features.
Some examples of the method, apparatus, and non-transitory computer-readable medium described herein may further include operations, features, means, or instructions for applying one or more weights to the physiological data and the set of features based at least in part on the activity the user associated with the wearable device may be engaged in, the at least one biometric associated with the user, or both and wherein obtaining the result from the machine learning model indicating the occurrence of the epileptic seizure event may be based at least in part on applying the one or more weights to the physiological data and the set of features.
In some examples of the method, apparatus, and non-transitory computer-readable medium described herein, the physiological data comprises one or more of an oxygen saturation associated with the user, a heart rate associated with the user, a temperature associated with the user, an optical perfusion associated with the user, or a movement pattern associated with the user.
In some examples of the method, apparatus, and non-transitory computer-readable medium described herein, the machine learning model comprises a neural network learning model, a decision tree learning model, a SVM learning model, or a combination thereof.
In some examples of the method, apparatus, and non-transitory computer-readable medium described herein, the indication of the epileptic seizure event comprises an audio output, a haptic output, a message output, or any combination thereof.
The description set forth herein, in connection with the appended drawings, describes example configurations and does not represent all the examples that may be implemented or that are within the scope of the claims. The term “exemplary” used herein means “serving as an example, instance, or illustration,” and not “preferred” or “advantageous over other examples.” The detailed description includes specific details for the purpose of providing an understanding of the described techniques. These techniques, however, may be practiced without these specific details. In some instances, well-known structures and devices are shown in block diagram form in order to avoid obscuring the concepts of the described examples.
In the appended figures, similar components or features may have the same reference label. Further, various components of the same type may be distinguished by following the reference label by a dash and a second label that distinguishes among the similar components. If just the first reference label is used in the specification, the description is applicable to any one of the similar components having the same first reference label irrespective of the second reference label.
Information and signals described herein may be represented using any of a variety of different technologies and techniques. For example, data, instructions, commands, information, signals, bits, symbols, and chips that may be referenced throughout the above description may be represented by voltages, currents, electromagnetic waves, magnetic fields or particles, optical fields or particles, or any combination thereof.
The various illustrative blocks and modules described in connection with the disclosure herein may be implemented or performed with a general-purpose processor, a DSP, an ASIC, an FPGA or other programmable logic device, discrete gate or transistor logic, discrete hardware components, or any combination thereof designed to perform the functions described herein. A general-purpose processor may be a microprocessor, but in the alternative, the processor may be any conventional processor, controller, microcontroller, or state machine. A processor may also be implemented as a combination of computing devices (e.g., a combination of a DSP and a microprocessor, multiple microprocessors, one or more microprocessors in conjunction with a DSP core, or any other such configuration).
The functions described herein may be implemented in hardware, software executed by a processor, firmware, or any combination thereof. If implemented in software executed by a processor, the functions may be stored on or transmitted over as one or more instructions or code on a computer-readable medium. Other examples and implementations are within the scope of the disclosure and appended claims. For example, due to the nature of software, functions described above can be implemented using software executed by a processor, hardware, firmware, hardwiring, or combinations of any of these. Features implementing functions may also be physically located at various positions, including being distributed such that portions of functions are implemented at different physical locations. Also, as used herein, including in the claims, “or” as used in a list of items (for example, a list of items prefaced by a phrase such as “at least one of” or “one or more of”) indicates an inclusive list such that, for example, a list of at least one of A, B, or C means A or B or C or AB or AC or BC or ABC (i.e., A and B and C). Also, as used herein, the phrase “based on” shall not be construed as a reference to a closed set of conditions. For example, an exemplary step that is described as “based on condition A” may be based on both a condition A and a condition B without departing from the scope of the present disclosure. In other words, as used herein, the phrase “based on” shall be construed in the same manner as the phrase “based at least in part on.”
Computer-readable media includes both non-transitory computer storage media and communication media including any medium that facilitates transfer of a computer program from one place to another. A non-transitory storage medium may be any available medium that can be accessed by a general purpose or special purpose computer. By way of example, and not limitation, non-transitory computer-readable media can comprise RAM, ROM, electrically erasable programmable ROM (EEPROM), compact disk (CD) ROM or other optical disk storage, magnetic disk storage or other magnetic storage devices, or any other non-transitory medium that can be used to carry or store desired program code means in the form of instructions or data structures and that can be accessed by a general-purpose or special-purpose computer, or a general-purpose or special-purpose processor. Also, any connection is properly termed a computer-readable medium. For example, if the software is transmitted from a website, server, or other remote source using a coaxial cable, fiber optic cable, twisted pair, digital subscriber line (DSL), or wireless technologies such as infrared, radio, and microwave, then the coaxial cable, fiber optic cable, twisted pair, DSL, or wireless technologies such as infrared, radio, and microwave are included in the definition of medium. Disk and disc, as used herein, include CD, laser disc, optical disc, digital versatile disc (DVD), floppy disk and Blu-ray disc where disks usually reproduce data magnetically, while discs reproduce data optically with lasers. Combinations of the above are also included within the scope of computer-readable media.
The description herein is provided to enable a person skilled in the art to make or use the disclosure. Various modifications to the disclosure will be readily apparent to those skilled in the art, and the generic principles defined herein may be applied to other variations without departing from the scope of the disclosure. Thus, the disclosure is not limited to the examples and designs described herein, but is to be accorded the broadest scope consistent with the principles and novel features disclosed herein.