A system for stimulating a muscle of a user, the system comprising: a stimulating unit comprising (i) at least two electrodes configured to be placed in electrical contact with skin of a user in a vicinity of the muscle, and (ii) a pulse generator configured to generate an electrical pulse for application to the muscle through the at least two electrodes; a sensing unit comprising at least one sensor configured to measure a physiological parameter of the user and generate a sensing signal in response thereto; and a control processor operatively coupled to the stimulating unit and to the sensing unit and configured to receive the sensing signal from the at least one sensor and change a parameter of the electrical pulse applied by the at least two electrodes in response to the sensing signal.

An unattended approach can increase the reproducibility and safety of the treatment as the chance of over/under treating of a certain area is significantly decreased. On the other hand, unattended treatment of uneven or rugged areas can be challenging in terms of maintaining proper distance or contact with the treated tissue, mostly on areas which tend to differ from patient to patient (e.g. facial area). Delivering energy via a system of active elements embedded in a flexible pad adhesively attached to the skin offers a possible solution. The unattended approach may include delivering of multiple energies to enhance a visual appearance.

A walking assist device includes a plurality of electrodes disposed on a surface of a leg of a user, a stimulation applier configured to apply, to the electrodes, a voltage for applying electrical stimulation to the muscles, and a control unit configured to control the stimulation applier to apply the voltage to one or more target electrodes selected from among the electrodes. The control unit controls the stimulation applier such that a combination of electrodes selected as the one or more target electrodes is different for each of a plurality of motion phases included in a motion cycle of the leg during the walking motion.

Devices for treating obstructive sleep apnea include appliances for securing to one or more teeth of a patient and connected to a lingual bridge configured to change shape and apply pressure to a patient's tongue, preventing backward movement of the tongue and blockage of the patient's airway. The lingual bridge is composed of a shape memory alloy to allow the bridge to change shape once deployed in a patient's oral cavity and exposed to increased temperature in the patient's mouth. Pulse generators and electrodes are included to electrically stimulate the nerves and muscles of the tongue to assist in keeping the tongue from moving backward in the mouth during sleep.

Provided is an electrical stimulation therapy apparatus for dysphagia including an input unit configured to receive user information including a food type divided into a low-viscosity liquid and a high-viscosity liquid, a stimulation unit including a plurality of channels and configured to stimulate swallowing muscles of a user, and a processor configured to generate a control command for driving the stimulation unit, wherein the processor sequentially stimulates the swallowing muscles including a bilateral suprahyoid muscle (SH), a thyrohyoid muscle (TH), and a sternothyroid muscle (StH) of the user according to a preset muscle activation sequence based on the user information.

A mobility assistance apparatus includes first and second frames positioned on left and right sides of a user; a hinge arm mechanism coupled to the first and second frames; and a pivotable securing unit or a walking seat coupled to the frames to transfer at least a portion of the user's body weight from the legs and to transfer weight through the user's hip or pelvis to the first and second frame enabling the user to stand or work for an extended period without requiring the user's arms to hold the frame; a wheel coupled to the first and second frames; a brake coupled to the wheel to provide friction to the wheel when actuated; and a tensioner coupled to the brake to adjust cable tension during wheel braking.

Provided are stimulation devices for improving ambulatory activity of a subject in need thereof. The device includes a foot covering for holding two battery-operated tactile actuators on a metatarsal region and an ankle region of the wearer's foot. The foot covering also includes a detachable material for housing and securing the two tactile actuators and a pouch region for holding electronics.

A telekinetic bionic glove assembly having a glove assembly, first and second boxes attached to the glove assembly, an arm box, and an electrical lead assembly connected to the arm box. The glove assembly has string guides positioned on glove fingers. The glove assembly also has a main bar and bands positioned at a glove back face, and a thumb splint. The first box has strings, motors, a motor controller, and reels. The second box has a voltage regulator, a battery, and a computer. The arm box has an arm box computer, an arm box voltage regulator, a bio-signal amplifier, an arm box battery, and arm box switch. The electrical lead assembly has electrical leads, lead heads, electrodes, and adhesive pads. The glove assembly operates, whereby the glove fingers open and close in response to voltage spikes as results of eye movements.

A method and system for behavioral neural learning in a user, including applying a first patch on a dermis of the user adjacent to a first nerve, the first patch comprising first electrodes, applying a second patch on the dermis of the user adjacent to a second nerve, the second patch comprising second electrodes, and generating a treatment protocol during a time period comprising applying a first electrical stimuli to the first nerve via the first electrodes of the first patch and applying a second electrical stimuli to the second nerve via the second electrodes of the second patch.

An electrical stimulation training and neuromuscular rehabilitation system including a machine-washable stimulation suit with multiple electrodes to provide controlled stimulation of various muscle groups is provided. The stimulation suit may also include one or more integrated biosensors to provide diagnostic capability in addition to stimulation. The system may also include a software platform executable on a user computing device (such as a tablet) that may facilitate control of the stimulation programs (e.g., intensity level, duration, isolation of individual muscle groups vs. full body stimulation) of one or more stimulation suits by the wearer or a fitness practitioner or trainer and/or that may facilitate intervention by a medical provider through a remote telemedicine platform.