The invention provides a method, a system and a computer program product to adjust an overall duration of a physical activity of a biological object. The physical activity is evaluated based on a physical activity parameter. The invention includes receiving: a target information (S1) corresponding to the physical activity parameter; the overall duration (S2) being a sum of a plurality of distributed time intervals; and a physical activity parameter information of the biological object. The physical activity parameter information is received (S4) for each distributed time interval. Thereafter, the corresponding distributed time interval is modified (S5) based on the received physical activity parameter information and the target information. Subsequently, a new overall duration (S8) of the physical activity is determined based on the modified distributed time interval and the received overall duration.

A computer implemented method for providing pain management using a wearable device determines a predictive model estimating an intensity level of pain as a function of at least one physiological parameter of a user of the wearable device and at least one activity of the user. The activity of the user includes one or combination of a type of the activity, a level of the activity, a location of the activity, and a duration of the activity. The method determines measurements of physiological and activity sensors of the wearable device to produce values of the physiological parameter and the activity of the user and predicts the intensity level of the pain based on the predictive model and the values of the physiological parameter and the activity of the user. The method executes actions based on the predicted intensity level of pain.

A technology for a wearable medical device for monitoring medical parameters. Medical measurement data can be received at the wearable medical device from a medical measurement sensor attached to the wearable medical device or a medical measurement sensor in communication with the wearable medical device. A calibration coefficient can be determined for calibrating the wearable medical device based on the medical measurement data. The wearable medical device can be calibrated based on the calibration coefficient.

A mobile device, methods and systems provide the invention mobile Personal Health Records (PHR) management platform solution. The platform enables secure PHR data management, measuring user's medical parameters, managing PHR secured depository containing user's health data on the user's invention combined phone & add-on sleeve device, while blocking none legitimate users access to the invention devices secured storage content. The invention device user's authentication is based on the combined weighted fusion of at least two different human biological sensors within the device and their weighted output analysis. The multi-sensors ensure bio-authentication secured memory entry only for the legitimate device user. In case of authentication success it activates various types of applications on the user PHR data depository content stored in device. The system supports the user's PHR remote health management, remotely monitoring the user's measured medical parameters, updating & managing user's health medical history depository in the user's electronic sleeve.

The non-invasive blood glucose level measurement device (1) is provided with a pulse waveform measurement unit (2) having FBG sensors (4) for measuring an acceleration pulse wave of a test subject; and a data-processing unit (3) for calculating the blood glucose level of the test subject at the point in time of measurement of the acceleration pulse wave, from waveform information of the measured acceleration pulse wave, on the basis of a predetermined correlation. The correlation is a calibration curve constructed by carrying out a PLS regression analysis, using the blood glucose level measured by a non-invasive blood glucose method as the objective variable, and a simultaneously-measured acceleration pulse wave as the explanatory variable. A non-invasive blood glucose level measurement device capable of measuring blood glucose level at about the same measurement accuracy as an invasive blood glucose measurement device can be achieved thereby.

The present disclosure generally relates to user interfaces for health applications. In some embodiments, exemplary user interfaces for managing health and safety features on an electronic device are described. In some embodiments, exemplary user interfaces for managing the setup of a health feature on an electronic device are described. In some embodiments, exemplary user interfaces for managing background health measurements on an electronic device are described. In some embodiments, exemplary user interfaces for managing a biometric measurement taken using an electronic device are described. In some embodiments, exemplary user interfaces for providing results for captured health information on an electronic device are described. In some embodiments, exemplary user interfaces for managing background health measurements on an electronic device are described.

The present disclosure describes a closed-loop fluid resuscitation and/or cardiovascular drug administration system that uses continuous measurements and adaptive control architecture. The adaptive control architecture uses a function approximator to identify unknown dynamics and physiological parameters of a patient to compute appropriate infusion rates and to regulate the endpoint of resuscitation.

This document discusses, among other things, apparatus, systems, or methods to efficiently collect heart sound data, including detecting first heart sound information of a heart of a patient using a heart sound sensor in a first, low-power operational mode, and detecting second heart sound information of the heart using the heart sound sensor in a separate second, high-power operational mode. The operational mode of the heart sound sensor can be controlled using physiologic information from the patient, including heart sound information, information about a heart rate of the patient, or other physiologic information from the patient that indicates worsening heart failure.

This document discusses, among other things, apparatus, systems, or methods to efficiently collect heart sound data, including detecting first heart sound information of a heart of a patient using a heart sound sensor in a first, low-power operational mode, and detecting second heart sound information of the heart using the heart sound sensor in a separate second, high-power operational mode. The operational mode of the heart sound sensor can be controlled using physiologic information from the patient, including heart sound information, information about a heart rate of the patient, or other physiologic information from the patient that indicates worsening heart failure.

A head guard is provided. The head guard includes one or more sensors as part of an sensory input and communications system. The head guard wirelessly communicates data to remote computing devices for intelligent data collection.