Abstract:
A rehabilitation assistance device (1), provided with: an arm part (30) having a holding part (20) for holding a part of the upper limb or the lower limb of a user, the arm part (30) movably supporting the holding part (20); a memory unit (80) for storing training information, the memory unit (80) storing first training information defined in advance; a motion information acquisition unit (61) for acquiring motion information associated with the movement of the holding part (20), the motion information acquisition unit (61) acquiring first motion information for the holding part (20) moved on the basis of the first training information; a motion evaluation unit (72) for generating evaluation information in which the motion information is evaluated, the motion evaluation unit (72) evaluating the first motion information and generating first evaluation information; and a display (40) for displaying at least one of the training information, the motion information, and the evaluation information.
Abstract:
A far infrared (“FIR”) sauna cabin equipped with a far infrared (“FIR”) heating elements constructed of ceramic, carbon, and/or light emitting diodes (“LED”), designed for therapeutic use in a sauna, capable of emitting far infrared energy, and heating an individual's skin for purposes of rejuvenation, anti-aging, weight loss, and acne therapy. The FIR heating element emits IR energy in a wavelength and frequency optimum for resonant absorption by the human body, resulting in the release of toxins stored within subcutaneous fatty deposits, which are then carried out of the person's system as he or she sweats. The FIR sauna is operated by a system comprising a local control system and a remote computer running access control software. A user account is configured containing a user's allowed privileges. When a user swipes an access card, the remote computer verifies the requested privilege. If allowed, the local system energizes the sauna system.
Abstract:
Intermittent pneumatic compression (IPC) devices facilitate fluid circulation in a body by providing alternating higher pressure and a lower or no pressure in an associated inflatable cuff. A source of air at a pressure less than 130% of the higher pressure at the inflatable cuff communicates to the inflatable cuff through a large-cross-section, continuously-open passageway. A large vent valve on that passageway opens for a lower or no pressure condition and closes to achieve a higher pressure within 0.1 second. For the lower or no pressure state, the vent valve not only vents the inflatable cuff, but also vents continuing air flow from the source of air pressure, until the next rapid pressure rise. The periods between successive compressions are from 2 to 10 seconds, with compressions from 0.35 to 5 seconds. While most of the inflatable cuff is not transparent, portions adjacent the heel and toes are.
Abstract:
A multipath-output-supporting evidence-based acupuncture and moxibustion acupoint therapeutic and detecting instrument and a using method thereof. The therapeutic and detecting instrument comprises a CPU core unit, a communication module, an audio module and a plurality of detecting, diagnosis and treatment circuits. The detecting, diagnosis and treatment circuit comprises an acupoint detecting unit and an acupoint acupuncture and moxibustion unit. The acupoint detecting unit comprises a resistance detecting circuit and an A/D digital converting circuit. The acupoint acupuncture and moxibustion unit comprises a D/A pulse current generating circuit and an amplifying circuit. The CPU core unit comprises an ARM processor, a memory, an auxiliary circuit and an evidence-based acupuncture and moxibustion therapeutic system, and the ARM processor is connected with the evidence-based acupuncture and moxibustion therapeutic system.
Abstract:
An ankle flexion and extension machine including a lower leg backing beam having upper and lower ends; a support arm cantilevering from the lower leg backing beam; an arm mounting pivot joint interconnecting the lower leg backing beam's lower end and the support arm's proximal end; a foot plate; a plate mounting pivot joint interconnecting the foot plate and the support arm's distal end, the plate mounting pivot joint being adapted for facilitating dorsiflecting and plantarflecting pivoting movements of the foot plate with respect to the lower leg backing beam; a reversible electric motor connected operatively to the foot plate, the reversible electric motor being adapted for driving the pivoting movement of the foot plate; a floor support base; and a triangulating frame supporting the lower leg backing beam, the support arm and the foot plate over the floor support base.
Abstract:
Many devices with “limbs” or “arms” are susceptible to damage when a user bends or twists a joint of the limb or arm beyond its design point or in a direction other than intended. This is common with children's toys. Accordingly, it would be beneficial to provide children with toys employing fluidic actuators that can be bent, twisted, deformed and yet recover subsequently allowing the intended motion to be performed. Further, it would be beneficial by providing devices that employ fluidic actuators, and hence are essentially non-mechanical, to provide users not only of toys but other devices with driving mechanisms that are not susceptible to wear-out such as, by stripping drive gears, etc., thereby increasing their reliability and reducing noise. Fluidic devices allow for high efficiency, high power to size ratio, low cost, limited or single moving part(s) and allow for mechanical springless designs as well as functional reduction by providing a piston which is both pump and vibrator.
Abstract:
In some embodiments, a kit may include systems allowing for clearing a biological airway. The kit may include an inner wearable system worn, during use, on a torso of a subject. The kit may include a plurality of engines which when activated apply an oscillation force to at least one treatment area of the subject. At least one of the plurality of engines may be releasably couplable to the inner wearable system. The oscillation force may be applied to at least one of the treatment areas of the subject such that the oscillation force mobilizes, during use, at least some secretions in an airway within the subject at least adjacent the treatment area. The kit may include an outer wearable system worn, during use, on a torso of a subject which when activated, adjusts the oscillation force. The kit may include one or more batteries and/or a control unit.
Abstract:
An adjustable air bladder apparatus is provided. The apparatus includes an outer enclosure, a first interior section within the outer enclosure that contains a plurality of air bladders, a second interior section within the outer enclosure that contains a support layer, and an air pump pneumatically coupled to the plurality of air bladders, where the air pump is configured to selectively supply pressurized air to the air bladders independently through a pneumatic coupling. The pneumatic coupling includes one or more supply valves, outlet valves, and pressure sensors coupled to each air bladder or to one or more groupings of air bladders. A control device is provided for monitoring the pressure within the air bladders and for controlling an amount of air provided to or released from the bladders or groupings of bladders. A method of providing rolling massage with the apparatus is also disclosed.
Abstract:
An adjustable foundation includes a base frame and an articulating frame movably supported by the base frame for longitudinal movement with respect to the base frame. A mattress platform is positioned on the articulating frame. A concealing assembly is positioned below the mattress platform and at least partially conceals the base frame. The concealing assembly is attached to the articulating frame for simultaneous longitudinal movement therewith.
Abstract:
Described here are devices, systems, and methods for treating one or more conditions (such as dry eye) or improving ocular health by providing stimulation to nasal or sinus tissue. Generally, the devices may be handheld or implantable. In some variations, the handheld devices may have a stimulator body and a stimulator probe having one or more nasal insertion prongs. When the devices and systems are used to treat dry eye, nasal or sinus tissue may be stimulated to increase tear production, reduce the symptoms of dry eye, and/or improve ocular surface health.