A cold therapy device for use in a water delivery system which is coupled to a mains water supply, the device includes a housing having an inlet for receiving water from a mains water supply, the housing includes at least one cooling module configured to reduce the temperature within the housing to cold therapeutic temperatures, so that, in use, when water is received therein from the inlet, it is cooled to cold therapeutic temperatures. The device further includes an outlet for delivering water from the housing to the user.

Devices and methods for tissue treatment produce a mechanical stimulation therapy and electromagnetic field therapy. The mechanical stimulation therapy provides stimulation of blood circulation and stimulates treated cells. The electromagnetic field enables thermal treatment of tissue. Combination of both therapies improves soft tissue treatment, mainly connective tissue in the skin area and fat reduction.

The invention relates to a method and apparatus for diagnosis, performance and/or regulation of physiological functions, in particular in an anaesthetized patient. The apparatus has a pressure device (10) for at least one body region or extremity (55) of a patient (50), wherein pressure-increasing means (21) and pressure-reducing means (22) are assigned to the pressure device (10), and a control device (30) is provided with which the pressure in the pressure device (10) can be controlled via the pressure-increasing means (21) and the pressure-reducing means (22).

The present invention relates to a system for assisting a person in walking, comprising a measurement unit for measuring physiological data including vital sign data and movement data of the person; an activity ability determination unit which is configured to determine a frailty state of the person based on the vital sign data, and to determine walking characteristics of the person based on the movement data; an activity program unit which is configured to select and continuously update a walking program based on the determined frailty state of the person and the determined walking characteristics of the person.

Disclosed is an electronic handheld device for performing a massage on a user. The device comprises a pair of handles that are substantially parallel to one another, each handle comprising a top and a bottom extremity, a shaft unit housing a shaft comprising a free extremity, the free extremity extending beyond the shaft unit, the shaft being substantially perpendicular to the pair of handles, a motor unit housing a motor, which drives the shaft, a trigger disposed on the primary handle, a trigger disposed in operative communication with the motor wherein, actuating the trigger results in the activation of the motor, and a massage head adapted to be mounted to the free extremity of the shaft whereby, the motion of the shaft is imparted to the massage head at which point, the massage head is applied over the skin of a user.

The vibration capsule device disclosed herein comprises a movement generation unit, a movement control unit, a wireless communication unit and a power supply. The movement control unit provides instructions to the movement generation unit, which generates movements in configurable frequencies and duty cycles. The power supply unit provides power to the movement generation unit through movement control unit, which also decides work period and rest period for the capsule device. The vibration capsule device further comprises a capsule movement detection unit, which comprises at least one sensor unit and provides information to the wireless communication unit.

Described herein are methods for determining a target musculoskeletal activity cycle (MSKC) to cardiac cycle (CC) timing relationship. The method may include detecting a signal responsive to a cyclically-varying arterial blood flow at a location on a head of a user; providing a recurrent prompt at a frequency of the heart pump cycle using the signal, such that the signal correlates with a magnitude of blood flow adjacent to the location, and the recurrent prompt is provided to guide the user to time performance of a component of a rhythmic musculoskeletal activity with the recurrent prompt; and guiding the user to adjust a timing of the component of the rhythmic musculoskeletal activity to substantially maximize a magnitude of the signal. In some embodiments, the method further includes generating the recurrent prompt by amplifying the sound generated by the blood flow in or in proximity to an ear of the user.

A Cardio Pulmonary Resuscitation (CPR) device, consisting of two distinct masseurs for chest and abdomen and a monitoring system for displaying patient's vital symptoms. The chest masseur works in controllable depth and speed, while the abdominal masseur applies pressure on abdominal aorta and Inferior vena cava in a contradictory rhythm with the chest masseur rhythm. This action causes more effective massaging by preventing overflow of blood to non-vital organs and accelerating return of blood to heart.

Systems and methods are provided for controlling infrared radiation (IR) sources of a sauna including tuning IR wavelength-ranges and radiated power-levels of IR sources, and directing IR to locations on a user's body. In one illustrative embodiment, a sauna may be provided having adjustable heat sources to emit IR at any wavelength resulting in a desirable radiation treatment for the sauna user. In another illustrative embodiment, a method is provided for tuning IR sources in a sauna.

An apparatus may be configured for documenting a code blue scenario when adhered to the chest of a subject undergoing resuscitation by sensing and transmitting information associated with the code blue scenario. Such information may include one or more of vital signs of the subject during resuscitation, information associated with chest movements of the subject during resuscitation, and audio information from an environment of the subject during resuscitation. A computing platform that is separate and distinct from the apparatus may provide code blue documentation conveying information related to the vital signs of the subject and derived from the audio information from the environment of the subject during resuscitation.