A method of conducting a stimulus treatment includes the steps of examining health conditions of a subject to obtain examination data information of the subject, registering the examination data information in an information accumulation device, planning a schedule of the stimulus treatment determined to be suitable for the subject based on the examination data, and conducting the stimulation application treatment by applying a stimulation to a stimulation receiving site of the subject with a stimulation application device so as to increase the blood flow in the subject by 60% or more after the application of stimulation, as compared to the blood flow before the application of the stimulation.

Apparatus and methods relate to a pneumatic compression therapy device configured to suggest content to the patient based on a determined disease state, the content pertaining to suggested changes in lifestyle based on a standard of care. In an illustrative embodiment, the suggested changes may include modifications to treatment location, treatment time, diet, eating habits, or sleeping schedule. Various examples may further sample the patient's health and automatically adjust a treatment parameter within a predetermined parameter range based on a history of measured parameters, such as limb volume, for example. In coordination with the therapeutic treatment, the therapy device may deliver suggested content to guide the patient to make more healthful lifestyle choices to reduce recovery time and improve patient health outcomes.

The present invention discloses a device for administering intermittent pneumatic compression (IPC) and Protocols of Artificially Induced Oscillations (PAIO) useful in alleviating peripheral circulatory disorders of a treated organ, comprising a wearable body portion enclosure (BPE) adapted to contact said treated organ, said BPE comprising: one or more balloons adapted to be inflated and deflated for creating said IPC; one or more pressure sources in fluid communication with said balloons by way of one or more valves; one or more vibrating elements adapted to produce PAIO; a controlling unit adapted to operate said pressure sources, and to operate said vibrating elements. The IPC and PAIO may be individually administered to said treated organ according to predetermined protocols.

A stool is provided that provides a raised heel squat position to a user that engages the stool. The raised heel squatting position promotes a healthy and productive experience on a toilet. The stool may be collapsible for easier storage and transportation. The stool may be adjustable to provide custom fittings to different size users. Additionally, the stool may be intelligent and may provide a customized immersive experience to a person on a toilet.

An example system includes a first wearable computing device, and at least one additional wearable computing device. The first wearable computing device is configured to retrieve information regarding a series of tasks to be performed in treating a patient in cardiopulmonary arrest. The information includes, for each task, an indication of a user to perform the task, an indication of a time point to perform the task. The first wearable computing device is further configured identify one or more subsets of the information, and transmit each subset to a different corresponding one of the additional wearable computing devices. Each additional wearable computing device is configured to receive, from the first wearable computing device, at least one of the one or more subsets of the information, and output, for each task within a received subset, a corresponding prompt to perform the task at the respective time point associated with the task.

A flexible anchor member comprising a member for placement about a body part; at least one substantially inextensible textile element circumscribing the member and secured to itself or the member; and a force transfer coupler coupling a portion of the at least one substantially inextensible textile element to an actuator such that the substantially inextensible textile element constricts about the member for a duration of an applied force. Another flexible anchor member comprising an outer member including a substantially inextensible textile material configured for directing a force applied by an actuator to act upon all or a portion of the body part; an inner member for positioning between the body part and the outer member, a first surface of the inner member configured for frictionally engaging the body part or intervening clothing; and at least one coupler for coupling the outer member and the inner member.

A soft-inflatable exosuit for knee rehabilitation is fabricated in two different beam-like structures (I and O cross-section actuators) and mechanically characterized for their torque performance in knee-extension assistance. The fabrication procedure of both types of actuators is presented as well as their integration into a light-weight, low-cost and body-conforming interface. To detect the activation duration of the device during the gait cycle, a soft-silicone insole with embedded force-sensitive resistors (FSRs) is used. In evaluation studies, the soft inflatable exosuit device is tested for its ability to reduce muscle activity during the swing phase of the knee. Using sEMG (surface electromyography) sensors, the rectus femoris muscle group of a healthy individual is recorded while walking on a treadmill at a constant speed, with and without the soft device.

Monitoring vital parameters of a wearer of a compression garment by analyzing a pressure signal waveform indicative of a fluid pressure in an inflatable and deflatable bladder of the compression garment. Analyzing the pressure signal waveform for an oscillating amplitude as a function of time and/or a representation of a pulse of the wearer provides an indication of blood pressure of the wearer.

A percussive therapy system includes a percussive therapy device that includes a housing, an electrical source, a motor positioned in the housing, a switch for activating the motor, a push rod assembly operatively connected to the motor and configured to reciprocate in response to activation of the motor, and an attachment configured to be operatively connected to a distal end of the push rod assembly of the percussive massage device and to provide at least one therapeutic effect to a user. The attachment may include at least one of an actuator configured to provide the at least one therapeutic effect to the user and a sensor configured to obtain at least one of biometric data of the user and information regarding operation of the percussive therapy device.

Systems, devices, and methods for determining a condition of a subject during cardiopulmonary resuscitation (CPR) are described herein. In an example method, a measurement of a physiological parameter of an individual is filtered and/or gated based on identifying a treatment administered to the individual. A condition of the subject is identified based on filtering and/or gating the physiological parameter. The example method can be implemented into a mechanical chest compression device or another portable medical device. Together, the methods can improve the monitoring and treatment of subjects receiving CPR.