A handheld device configured to provide tactile stimulation to a head of a human user. The handheld device comprises an outer housing sized and shaped to fit ergonomically and substantially within a hand of the human user. The outer housing defines an internal space and skin facing surface for placement adjacent to or proximate the user's head. A controller is contained within internal space of the outer housing, wherein the controller is configured to generate a signal corresponding to a pattern sequence. A vibration unit is in electronic communication with the controller, the vibration unit being configured to be actuated in response to a signal from the controller so as to generate vibrations that correspond to the pattern sequence.

In an assistance apparatus, when assisting a user in walking with an object, a motor generates, in a gait phase of a left leg, a tension less than a second threshold value in a first wire during a fifth period other than a first period during which a tension greater than or equal to a first threshold value is generated in the first wire, and a tension greater than or equal to the second threshold value in a second wire during a sixth period other than a second period during which a tension greater than or equal to the first threshold value is generated in the second wire, and generates, in a gait phase of a right leg, a tension less than the second threshold value in a third wire during a seventh period other than a third period during which a tension greater than or equal to the first threshold value is generated in the third wire, and a tension greater than or equal to the second threshold value in a fourth wire during an eighth period other than a fourth period during which a tension greater than or equal to the first threshold value is generated in the fourth wire.

A belt for use in a BFR system with an outer belt material hermetically sealed to an inner belt material along a perimeter, thereby forming at least one inflatable chamber, the inflatable chamber having an input port for accepting a gas into the chamber, the belt further comprising a first fastening means in communication with the outer belt material, for attaching to a second fastening means in communication with the outer belt material, thereby locking a circumference of the belt, when wrapped around a user's limb, and the belt further comprising a pre-tensioning system for prescribing and applying a known amount of initial compression to the limb by the belt.

A massage mechanism includes a portion, which, in a muscle hardness measurement mode, drives an advancing/retreating motor to rotate in a predetermined direction by constant-speed control to press a massage element into a body of a person to be treated, a portion monitoring a change rate of a motor current flowing through the advancing/retreating motor during driving of the advancing/retreating motor and stopping the driving of the advancing/retreating motor when the change rate of the motor current becomes not less than a predetermined threshold, a portion, which, after stoppage of the driving of the advancing/retreating motor, drives a tapping motor to rotate by constant-speed control to make the massage element perform a tapping operation, a current detection portion, detecting a motor current flowing through the tapping motor during driving of the tapping motor, and a portion measuring a muscle hardness of the person to be treated based on the motor current detected by the current detection portion.

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.

A method and apparatus to detect environmental triggers of stress and antecedent physiological stress symptoms of a patient, followed up with delivery of stress relieving therapeutic response to the patient and a chronological report of events. An embodiment comprises a first device worn by the patient that contains sensors and can transmit and receive signals and a second device used by the caregiver that can transmit and receive signals. This integrated system continuously monitors environmental triggers and physiological stress indicative parameters of a patient diagnosed with autistic spectrum disorder, or other emotional or physical disorders, and compares these parameters against thresholds for the parameters. These thresholds can be configured automatically by the systembased on past episodesor manually by the caregiver, or using automatically configured thresholds that are fine-tuned by the caregiver. When the parameters exceed the configured thresholds, several responses can be automatically generated by the system including: 1) generating therapeutic calming responses and cues to the patient to alleviate the episode, 2) sending notifications to the caregiver's device for intervention, and 3) creating a chronological assessment report of environmental stress triggers, antecedent physiological stress symptoms, and the resultant behavior of the patient.

Embodiments disclosed herein relate to a garment system including at least one sensor and at least one actuator that operates responsive to sensing feedback from the at least one sensor to cause a flexible compression garment to selectively constrict or selectively dilate, thereby compressing or relieving compression against at least one body part of a subject. Such selective constriction or dilation can improve muscle functioning or joint functioning during use of motion-conducive equipment, such as an exercise bike or rowing machine.

A therapeutic spectacles device for reliving symptoms of dry eye disease. The device includes a protective housing configured to house a stimulus mechanism and an internal power source; at least one contact pad attached to the protective housing; and an attachment mechanism arranged on the protective housing. The at least one contact pad is configured, to contact a targeted area within a region selected from patient's nasofrontal region, supraorbital region, suborbital region, temporal region, or any combination of the same. The attachment mechanism can be configured to fix the protective housing to the therapeutic spectacles device such that the at least one contact pad rests against the targeted, area, when the therapeutic spectacles device is fixed on spectacles worn by the patient. The stimulus mechanism can be configured to deliver a stimulus through the at least one contact pad to the targeted area.

An apparatus can include a left cover, sized and shaped to fit over a left eye of a patient to define a left cavity between the left cover and an anterior surface of the left eye and a right cover, sized and shaped to fit over a right eye of the patient to define a right cavity between the right cover and an anterior surface of the right eye. The apparatus can include a left pressure source to apply a left working fluid to the left cavity, the left pressure source capable of generating a left cavity pressure including a left negative gauge pressure and a right pressure source to apply a right working fluid to the right cavity, the right pressure source capable of generating a right cavity pressure including a right negative gauge pressure, where the right pressure source can be separate from the left pressure source. The left pressure source can be configured to generate a left cavity pressure independently of the right pressure source and the right pressure source can be configured to generate a right cavity pressure independently of the left pressure source.

Systems, and methods relate to a medical device receiving a treatment parameter operating point within a first operating region defined by a first set of operating points for which automatic incremental adjustment of a parameter in the current operation is permitted. In an illustrative example, incremental adjustment may use artificial intelligence based on patient feedback and sensor measurement of outcomes. Some exemplary devices may receive a request to alter the current treatment parameter operating point to a second treatment parameter operating point outside the first operating region and in a second operating region in a known safe operation zone, bounded by a known unsafe zone unavailable to the user. In the second operating region, some examples may restrict the step size of incremental adjustments requested by the user. Data may be collected for cloud-based analysis, for example, to facilitate discovery of more effective treatment protocols.