A method and method for a cloud-based gaming platform with integrated healthcare diagnostic and treatment capabilities. In an embodiment, the system and method comprise a cloud-based gaming platform comprising a frontend accessible from various game clients which operates a gaming environment on one or more game servers, a backend that provides the game database and analytics used by the game servers to operate the gaming environment, and a healthcare diagnostics and treatment module integrated into the platform comprising a HIPPA-compliant security gateway, an AI-assisted healthcare diagnostics module, and an alert and treatments module. Exercising on an exercise machine compatible with the cloud-based gaming platform entertains the user while simultaneously capturing data about the user’s physical and mental performance which can be used to diagnose medical conditions and, depending on configuration, implement treatment regimens comprising exercise routines and mental simulation via tasks in the gaming environment.

A remote alarm for use with a wearable medical device. The remote alarm is configured to receive alarms, voice messages and prompts issued by the wearable medical device and to repeat those alarms, voice messages and prompts in a manner that can more easily be perceived by a patient wearing the wearable medical device or a bystander. The remote alarm can be configured to receive a communication from the wearable medical device, and in response, to identify one or more messages to be provided to the patient or a bystander. The messages may be provided audibly, visually, tactilely or combinations thereof. The remote alarm may further be configured to take certain actions depending upon the content of the communication, such as sending a telephone message to alert emergency personnel to the identity, location and medical condition of the patient, or sending an email.

A tissue hydration monitor and method includes a sensor module having a plurality of LEDs positioned to emit a plurality of different wavelengths of light toward the user's skin and a detector that detects light transmitted and reflected through the user's skin to generate signals corresponding to an intensity of detected light at each of the different wavelengths. A processor/controller module generates a baseline hydration level based on the received signals, calculates a relative hydration level, and generates an output indicative of relative hydration personalized to the user. The housing is secured against the user's skin by an adhesive patch or a strap.

An apparatus for estimating bio-information includes: an impedance sensor including a pair of input electrodes and a pair of receiving electrodes, and configured to measure bio-impedance of a user by applying a current to the pair of input electrodes and by measuring a voltage between the pair of receiving electrodes; and a processor configured to estimate bio-information by applying, to the measured bio-impedance, an estimation model that uses a correlation between the measured bio-impedance and the bio-information to be estimated.

An ablation catheter Has a spring assembly residing between an ablation head and a proximal catheter body. Three optical fibers extend through a lumen in the catheter body. Three mirrors supported by the ablation head face proximally but are spaced distally from the optical fibers. The mirrors are provided with a pattern of reflectance that varies along a radius from a central area of reflectance. Light of a respective defined power shines from each of the optical fibers to a corresponding one of the mirrors with a reflected percentage of the respective defined light power being reflected back to the optical fiber. A percentage of the reflected percentage of the respective defined light power is captured by and travels along each optical fiber to a dedicated light wave detector connected to a controller. From the percentage of the reflected percentage of the light of the respective defined power received by each detector, the controller is programmed to calculate whether an axial or lateral force is imparted to the ablation head and, if so, the magnitude and vector of those forces.

A health monitoring system and corresponding method for monitoring a physiological condition of a user may include collecting, by a monitoring device, measurements representing physiological signals of the body, transmitting the measurements from the monitoring device to a local device, and receiving, at a remote server, the measurements and additional data from the local device. The remote server may include a processing module, a review portal and a clinician portal, such that the remote server may be arranged to automatically classify the measurements representing physiological signals of the body, verify the classifications, and provide the verified measurements at a clinician portal.

A dry electrode and a physiological multi-parameter monitoring equipment are disclosed. The waterproof dry electrode comprises an encapsulation, extraction electrode and a contact surface layer, wherein the extraction electrode and the contact surface layer are connected with each other and disposed in the encapsulation; the contact surface layer comprises an exposed part and an embedded part encapsulation; the encapsulation comprises flexible silica gel and hard plastic portion, the embedded part being embedded into the hard plastic portion, and the hard plastic portion being packaged in the flexible silica gel. Through the above arrangement in the present invention, the dry electrode can reach a waterproof grade of IPX7, which is higher than living waterproof grade of an ordinary dry electrode. The PMPME can be a patch-type acquisition and monitoring equipment which is convenient for long time wearing and physiological multi-parameter monitoring, with excellent sealing and waterproofness, and the electrode is reusable.

Methods, apparatus, and systems relating to a Wearable Cardioverter Defibrillator (WCD) system capable of logging event data and/or broadcasting state changes and/or system status information to external clients are described. In an embodiment, a processor stores data corresponding to one or more event markers in memory in response to occurrence of an event. Occurrence of the event is detected based at least in part on detection of one or more parameters by one or more sensors or a signal to be generated by one or more of electrodes of the WCD system. A communication device transmits at least a portion of the stored data to a remote device. A patient condition or a WCD system condition can then be detected based at least in part on analysis of the stored data and/or the transmitted portion of the stored data.

Techniques are described for integrating blood pressure measurement (BPM) into a portable electronic device. For example, an input interface of the device includes an integrated force sensor. Human-discernable feedback is output to the user, while using the force sensor to monitor fingertip pressure being applied by the user on the input interface, to guide the user into a first condition in which capillary fingertip blood flow (CFBF) is occluded. The human-discernable feedback is then output to the user, while continuing to use the force sensor to monitor the fingertip pressure, to guide the user into one or more subsequent conditions that allow non-occluded CFBF signals to be sensed by one or more sensors (e.g., the force sensor, an optical fingerprint sensor, etc.). The sensed non-occluded CFBF signals can be used to generate one or more CFBF-based BPM readings for the user (e.g., which can be calibrated to arterial BPM).

A system, method, and computer platform product for an adaptive cognitive training platform. In accordance with various aspects of the present disclosure, an adaptive cognitive training platform is configured to process user activity data from one or more instances of a computerized cognitive training program to determine a baseline cognitive assessment for one or more cognitive abilities/skills of a user. The cognitive assessment model may be configured to further process the user activity data to predict a relative value or measure of efficacy for one or more computerized stimuli or interactions within the computerized cognitive training program. The adaptive cognitive training platform may be configured to configure, modify and/or present one or more graphical user interface elements for one or more subsequent instances of the computerized cognitive training program according to the predicted value or measure of efficacy of one or more cognitive training tasks.