A wearable device and an exercise support method performed by the wearable device are disclosed. The exercise support method includes receiving exercise setting information associated with a lower body muscle that is selected by a user input, determining a torque profile to be applied to the wearable device based on the received exercise setting information, and operating an actuator of the wearable device based on the determined torque profile.

A method of measuring muscular fitness of a user using a wearable device includes determining a target resistance profile for a target movement to be performed by the user wearing the wearable device to measure muscular fitness, controlling a motor driver circuit of the wearable device based on the target resistance profile to control a resistance force to be provided to the user, measuring state information of an actual movement performed by the user under the resistance force, and measuring the muscular fitness of the user based on the state information.

A toe correction apparatus and a method for manufacturing the same are provided. The toe correction apparatus includes: a first sensor attachable to a first side of a hallux proximate to a second toe for measuring first pressure information between the hallux and the second toe; and a processor, configured to determine a degree to which the hallux bends to the second toe according to the first pressure information, and control an inflation amount or a deflation amount of an adjustable airbag between the hallux and the second toe according to the degree to which the hallux bends to the second toe.

Systems and methods for recording data representative of, and reviewing and analyzing such data for, compliance by patients with prescribed use regimens of rehabilitation devices, such as a sling, are disclosed. Such devices comprise one or more sensors, a power source, and a communication system. The sensors track data indicative of the actual wear or use time of the rehabilitation device, which may be used to monitor compliance with physician recommended wear times. Adjustments may then be made to the prescribed use regimen, or physical adjustments may be made directly to the rehabilitation device.

A medical device for assessing and/or rehabilitating a human joint of an extremity includes a joint brace comprising a first support for coupling to an upper part of the extremity, a second support for coupling to a lower part of the extremity, and a rotatable joint connecting the first and second supports, and a mechanical device coupled to the first and second supports, the mechanical device configured for moving one or more of the first and second supports so as to rotate about the joint. In another alternative the medical device can include sensors located for making angle measurements between the first and second supports and for recording movement data and a computing device for receiving and storing the angle measurements and the movement data and for transmitting said data via a radio transmitter.

A device for performing individual movement analysis and movement therapy on a patient includes a control and analysis unit configured to control a first intervention device in such a way that a first trajectory of the movement of an extremity of the patient is disrupted by a force exerted by a movement module onto the extremity of the patient. A response to this disruption is measured by changed measured values from at least one force sensor and/or at least one angle sensor, and a new, second trajectory is calculated therefrom. New control parameters for controlling the first intervention device are calculated from a comparison of the second trajectory with the first trajectory and/or a target trajectory or the comparison of the disrupted measured values with the non-disrupted measured values.

The present disclosure provides generally for a therapeutic oral device for sleep apnea and associated methods for using the device. According to the present disclosure, the device may comprise a hard palate portion, mouth guard portion, and a tongue retainer portion. The hard palate portion may comprise one or more materials. The hard palate portion may also comprise a composite of materials, including but not limited to embedded materials. The mouth guard portion may comprise one or more components that provide stability and maintain the position of the therapeutic oral device within the mouth. The tongue retainer portion may comprise an airway and a predetermined length. A method of use may comprise the utilization of one or more incremental oral devices to overcome a gag reflex. When the oral device is formed from a mold, the mouth guard portion and the hard palate portion may be custom fit to the dimensions of the intended mouth.

Exosuits that use core grip members are described herein. Core grip members apply forces in a radially inward manner from the exterior of the body to the interior of the body to provide support to the user and to serve as a platform for mounting power layer segments.

Systems, methods, and apparatuses for performing analytics for equine-related conditions from fetlock sensors include receiving sensor data from one or more sensors attached to one or more fetlock wearable devices. Each of the one or more fetlock wearable devices are configured to attach to a fetlock of a respective limb of a horse. The analytics system compares the sensor data to one or more baseline measurement values. The analytics system detects a condition responsive to comparing the sensor data to one or more baseline measurement values. The analytics system transmits an alert to one or more remote devices responsive to detecting the condition.

Methods are disclosed for measuring the size of body parts treated by a compression therapy device. Either the volume or circumference of the body part may be measure. The methods my include evacuating an inflatable compression sleeve to a known pressure, inserting the body part into the compression sleeve, inflating the sleeve to a pre-set condition, and then measuring one or more inflation related parameters. The pre-set conditions may include a predetermined pressure, volume, or size of the inflatable cells comprising the sleeve. The inflation related parameters may include the time to fill the cell to a pre-set pressure, the pressure attained after a pre-set time of inflation, or the measure volume of a cell after a pre-set amount of air is introduced into it. The methods may also include deflating the cells from the known inflation state to a second inflation state and measuring similar parameters.