A device is provided for manipulating an arm of a user, thereby providing extension or flexion assistance to the arm about an elbow. The device has an arm engagement system, having an upper arm member with an upper arm frame having a pivot end and a distal end, a posterior elbow pad, a forearm member with a forearm frame having a pivot end and a distal end and a distal wrist pad, and a pivoting connection operatively coupled with the pivot end of the upper arm frame and the pivot end of the forearm frame. A force application system having a force applicator is connected between the distal end and the pivot end of the forearm frame. A force application mechanism is connected at or near the distal end of the upper arm frame.

The present disclosure relates to the field of medicine and discloses a medical therapeutic device for monitoring and treating medical condition of patients. The device comprises an input unit, a plurality of sensors, a control unit, a waveform generator unit, and a coupling means. The input unit receives at least one input from a user. The sensors monitor a plurality of predetermined parameters associated with the health of a patient generate detection signals based on the monitored parameters. The control unit selects a program based on the input and the detection signals. The waveform generator unit generates a therapeutic signal of pre-determined values of at least one of voltage, current, and frequency based on the selected program for facilitating treatment of medical condition corresponding to the selected program.

A system for monitoring performance of a resuscitation activity on a patient by an acute care provider is provided. The system includes: a first wearable sensor configured to sense movement of a first portion of an acute care provider's hand; a second wearable sensor configured to sense movement of a second portion of the acute care provider's hand; and a controller. The controller is configured to: receive and process signals representative of performance of a resuscitation activity from the first sensor and the second sensor; identify from the processed signals information indicative of at least one of a relative distance, a relative orientation, a change in relative distance and a change in relative orientation between the first sensor and the second sensor during performance of the resuscitation activity; and determine at least one resuscitation activity parameter based, at least in part, on the identified information.

The present disclosure provides a finger joint rehabilitation training device, which includes a control member, a data acquisition member, a gas circuit system, and a wearable training member. The wearable training member is provided with a pneumatic component that can expand and contract. The data acquisition member is configured for acquiring hand motion information of a first hand and transmitting the hand motion information to the control member. The hand motion information includes hand pressing information. The control member controls the gas circuit system to inflate the pneumatic component or to draw air from the pneumatic component according to the hand motion information, to make the wearable training member change between a flexion condition and a stretching condition, so as to realize a hand mirror training of a second hand. The hand pressing information is simple and convenient to acquire, which is convenient for the first hand to realize the flexion condition and the stretching condition, and the condition of the second hand is adjusted through the condition of the first hand, so that the wearable training member can be better adjusted, different hand training intensity requirements are met, and a better training effect is achieved.

A bathing apparatus comprising a whirlpool pump; a heater; an air blower; a drain pump; and an electric module, wherein the electric module is configured to receive electric power from an electric power line and to distribute electric power to the whirlpool pump, heater, air blower, and drain pump, when electric power is distributed to one of the heater or the air blower, electric power cannot be distributed to the other of the heater or the air blower, and when electric power is distributed to the drain pump, electric power cannot be distributed to the whirlpool pump, the heater, and the air blower.

A wearable device, includes a motor, a motor driver circuit, a memory, a sensor, and a processor. The memory is configured to store resistance force generation setting information indicating a difference between a reference angle and each joint angle and a corresponding relationship between respective duty ratios. The processor is configured to obtain, using the sensor, a joint angle of a user and calculate a difference between the reference angle and the obtained joint angle. The processor is configured to obtain a duty ratio corresponding to the calculated difference according to the resistance force generation setting information. The processor is further configured to provide a control signal having the obtained duty ratio to the motor driver circuit to perform control such that a control state of the motor driver circuit is switched between a first control state and a second control state.

A method of connecting a user device anonymously to a remote operator, via an intermediate anonymizing server is described. In this way, a remote operator may control the device, without the remote operator knowing the identity of the owner or of user of the device. A remote operator might provide medical support or entertainment. The user of the device is provided with a connection key, which is then further given by the user to a desired remote operator. Both the user and the remote operator provide the anonymizing server with the connection key. The anonymizing server opens a chat room uniquely associated with the connection key. Electronic connectivity is provided by forwarding messages between the user device and the remote operator through the chat room. No other access to the chat room is permitted. The anonymizing server does not store the connection key. No user application is required.

In one aspect, an electronic device for promoting proper use of a walking aid during lower extremity injury rehabilitation comprises at least one load sensor configured to measure a load on the walking aid. A memory stores rehabilitation program data defining at least one time interval of a rehabilitation period and, for each time interval, a target load for the walking aid during the time interval. A currently operative time interval of the at least one time interval of the rehabilitation period is identified. Data is received, from the load sensor(s), indicative of a dynamic load on the walking aid during a patient step. Based upon the received data, a peak load upon the walking aid during the patient step is determined. A user notification indicating that the peak load is non-compliant with the target load for the walking aid for the currently operative time interval is provided.

Resuscitation and ventilation monitoring devices are provided. A device includes an inlet in fluid communication with airflows exchanged with lungs of a patient and an airflow meter for measuring characteristics of the airflows. A user may provide a controller with patient information, e.g., height, weight, gender, or age, via a measurement selector, enabling the controller to determine acceptable ranges of measured airflow characteristics. The device may determine a current mode of ventilation and associated ventilator settings based on the measured airflow characteristics. The device may also identify and filter out artifacts present in the ventilation signal, and determine whether a respiratory failure phenotype is present in the ventilation. If the current mode of ventilation and associated ventilator settings fall outside an acceptable range, the ventilation is classified as off-target and the controller may cause a sensory alarm to alert the user. The device may suggest a corrective action based on the type of off-target ventilation detected. The device may also continuously analyze ventilation to determine changes in lung compliance over time and to identify pathological changes over time. The device may work within a network of devices and user interfaces via wired or wireless communication, and is not restricted to or dependent on the type of ventilatory device with which a patient is being supported.

A method and system of sleep maintenance includes configuring a stimulation device comprising a transducer to emit a transcutaneous vibratory output to a body part of a subject, receiving physiological data of the subject from at least one sensor at a processor, providing a stimulation pattern for the transcutaneous vibratory output to be emitted by the transducer, the stimulation pattern comprising a perceived pitch, a perceived beat, and an intensity of the transcutaneous vibratory output, causing the transducer to emit the transcutaneous vibratory output in the stimulation pattern, determining a sleep state of the subject based on the physiological data, and altering the stimulation pattern based on the sleep state, wherein altering comprises at least one of (i) reducing a frequency of the perceived pitch, (ii) increasing an interval of the perceived beat, or (iii) reducing the intensity.