Abstract:
The present invention is directed toward a device for circumduction of a limb having a base, a vertical support operably coupled to and extending away from the base, a rotary member operably connected to the vertical support, a limb support member operably connected to the rotary member, and a motor drivingly engaged with the rotary member. The vertical support may be a rigid plate member, bracket, or frame. The bracket and/or frame may include at least one vertical member and at least one horizontal member. The rotary member is operably connected to the vertical support such that rotary member is free to rotate. Limb support member receives and supports the limb to be treated and is operably coupled to rotary member at a radial distance from a center of rotation thereby resulting in a circular motion of a limb when the motor is operated.
Abstract:
A apparatus includes an a exoskeleton system with a plurality of sensors for generating signals indicating a current motion and a current arrangement of at least the exoskeleton system, a hip segment, and at least one lower limb. The lower limb includes thigh and shank segments for coupling to a lateral surface of a user's leg. The thigh segment includes a first powered joint coupling the thigh segment to the hip segment, a second powered joint coupling the thigh segment to the shank segment, and a controller coupled to the sensors, the first powered joint, and the second powered joint. The controller is configured for determining a current state of the exoskeleton system and a current intent of the user based on the signals and generating control signals for the first and second powered joints based on the current state and the current intent.
Abstract:
A combined heating, cooling, and compression therapy system is provided. The system is configured for automated use with a controller. The system can have a core with separate channels for providing cold and heat and compression therapy; a cover for receiving the core; and a skin sensitive temperature node attached to the core cover.
Abstract:
A method for treating urinary incontinence is provided. The method includes providing a device having an expandable portion having an outer surface, a first electrode, and a second electrode, the first and second electrodes coupled to the outer surface of the expandable portion and configured to cause a contraction of a muscle in communication with the electrodes. The method further includes causing the expandable portion to inflate such that the first and second electrodes contact vaginal walls and causing a contraction of a muscle in communication with the electrode.
Abstract:
A method of operating a portable, foldable, and multifunctional mobility aid apparatus that assists a user in standing, sitting, and/or walking process. The apparatus has an integrated power source and is based on 4 wheels. Users can stand on it and drive it as an electric mobility device, or disable it and use it as a passive walker. The apparatus has a pair of supporting beams with adjustable width to be placed under the user armpits and support the user in standing up, sitting down, and/or moving around. The apparatus can be controlled by a control panel mounted on a pair of handles, and its functions can be controlled by the user with no need for help from another person. The apparatus can be minimized by a combination of multiple telescopic vertical minimization mechanisms and multiple folding mechanisms.
Abstract:
A method of automatically determining which type of treatment is most appropriate for a cardiac arrest victim, the method comprising transforming one or more time domain electrocardiogram (ECG) signals into a frequency domain representation comprising a plurality of discrete frequency bands, combining the discrete frequency bands into a plurality of analysis bands, wherein there are fewer analysis bands than discrete frequency bands, determining the content of the analysis bands, and determining the type of treatment based on the content of the analysis bands.
Abstract:
The invention relates to a monitoring system for monitoring CPR performance and a reference unit for use in the system. The system comprises a measuring unit for positioning on the chest of a patient or manikin monitoring the movements applied to the chest, wherein the system also comprises a reference unit, the reference unit comprising sensors for measuring the movements thereof, wherein said units comprises means for wireless communication, one of the units comprising a signal analyzing means and a signal receiver coupled thereto for receiving said wireless communication, and the other unit comprising a signal transmitter for transmitting the measured signals to the signal receiver.
Abstract:
Methods and systems for dynamic compression of venous tissue enable improved blood movement in the extremities. In accordance with an exemplary embodiment, a pressure pad provides a compressive force to the venous plexus region of the foot. The pressure pad is successively withdrawn and re-pressed against the foot. Improved blood circulation may reduce the occurrence of undesirable complications such as deep vein thrombosis, ulcers, and the like.
Abstract:
A system and process including a transponder and a hand-held transducer having a pulse delivery assembly and a sound pressure wave generating device driven by an electronics package. The electronics package is capable of outputting prerecorded programs, to the sound pressure wave generating device, upon receiving an instruction from the transponder. The electronics package responds to instructions by retrieving a labeled and stored prerecorded audio program and driving the sound pressure wave generating device. The sound pressure wave generating device is mechanically linked to a pulse delivery assembly having a hammer pad with attached permanent magnets. The pulse delivery assembly vibrates the hammer pad, which administers therapeutic patterned percussive pulses and a patterned fluctuating magnetic field through direct contact on the skin of a subject, according to the prerecorded program. Upon being disposed proximate to the electronics package, the transponder is configured to automatically establish communication and provide the instruction.
Abstract:
The present technology is the use of the combination to treat a patient and the treatment of a patient. Sine waves are generated digitally by the combination. Data validation is used to ensure correct directional alignment prior to device activation. Patient safety and consistency in treatment protocols are considered in the spinal and upper cervical impulse treatment design. A patient is treated with smooth sinusoidal waveform with a force of about 8 N to about 12.2 N with a Z-axis of acceleration (shear acceleration) of about 0.5 g to about 5g at about 5 Hertz (Hz) to about 200 Hertz. Treatment conditions can be varied depending upon the size of the patient, which includes human and veterinary patients. The method is non-invasive.