Tumors in portions of a subject's body that have a longitudinal axis (e.g., the torso, head, and arm) can be treated with TTFields by affixing first and second sets of electrodes at respective positions that are longitudinally prior to and subsequent to a target region. An AC voltage with a frequency of 100-500 kHz is applied between these sets of electrodes. This imposes an AC electric field with field lines that run through the target region longitudinally. The field strength is at least 1 V/cm in at least a portion of the target region. In some embodiments, this approach is combined with the application of AC electric fields through the target region in a lateral direction (e.g., front to back and/or side to side) in order to apply AC electric fields with different orientations to the target region.

A collar-mounted location sensor and stimulation unit includes a body. A generally planar stimulation unit and differential impedance-based fur detector in combination protect the animal from harmful stimulation. At least one sensory stimulator is configured to provide at least one of auditory, kinesthetic, and visual stimulation responsive to an output of a location sensor. One or more of a voltage, current, oscillation frequency, extent of modulation, or other output characteristic of the stimulation unit output is varied responsive to the detected fur differential impedance to protect and benefit both the body and mind of the animal.

The present invention is directed to transcutaneous electrical nerve stimulation (TENS) devices which utilize novel stimulation waveforms and novel arrangements of TENS electrodes to improve the efficiency of power consumption while enhancing therapeutic effects.

A wearable device for facilitating neurophysiological treatment of a patient harboring an implanted neural stimulator is provided. The wearable device includes a transmitting antenna configured to accept one or more input signals and to transmit one or more electromagnetic signals to a neural stimulator that is implanted in a patients body. The wearable device further includes a control circuitry configured to provide the one or more input signals to the transmitting antenna. The wearable device further includes a battery that provides electrical power to at least the control circuitry. The wearable device is configured to be worn outside the patient's body.

The present disclosure relates to an acupoint stimulation device and an acupoint stimulation method using the same. The acupoint stimulation device includes: a power supply unit configured to supply power; a controller configured to generate an electrical stimulus signal applied to a skin of the subject; and an electrical stimulation unit including two or more electrodes configured to receive power from the power supply unit and to supply the stimulus signal to the acupoint area, wherein the electrodes are arranged in a state of being electrically insulated from each other and are in electrical contact with the skin of the subject. Thereby, it is possible to provide an appropriate amount of stimulation required for treatment and symptom relief by providing stimulation to an accurate acupoint position.

Systems and methods are described herein for selection of a cardiac cycle, or heartbeat, from a plurality of cardiac cycles monitored over time. The cardiac cycle may be selected using various metrics including a single-cycle metric and a cycle-series metric. Further, the selected cardiac cycle may be used for further cardiac analysis (for example, to generate electrical activation times).

The electronic device using a low frequency according to an embodiment of the present disclosure may include: a belt; a cable including a first line extending in a first direction and a second line extending from between one end and the other end of the first line in a second direction crossing the first direction; a first pad detachably attached to a rear surface of the belt and connected to the one end of the first line on the rear surface of the belt; a second pad detachably attached to the rear surface of the belt and connected to the second line on the rear surface of the belt; and a control box detachably attached to the belt and including a processor, wherein the other end of the first line passes through the belt and is connected to the control box on the front surface of the belt, and a position to which the first pad is attached on the rear surface of the belt and a position to which the second pad is attached on the rear surface of the belt are adjustable.

A muscle stimulation assembly includes a plurality of sleeves that is each wearable on a selected limb on a user's body. Each of the sleeves is comprised of a resiliently stretchable material thereby facilitating the sleeves to compress around the selected limb. A plurality of conduction arrays is each integrated into a respective one of the sleeves. Moreover, the conduction array in the respective sleeve engages skin on the limb when the respective sleeve is worn and is in electrical communication with muscles in the limb when the respective sleeve is worn. A control system is placed into selective electrical communication with the conduction array in the respective sleeve when the respective sleeve is worn. The control system generates an electrical impulse and communicates the electrical impulse to the conduction array in the respective sleeve to flex muscles in the limb for therapeutic purposes.

A control system for a movement reconstruction and/or restoration system for a patient, comprising a CNS-Stimulation Module, especially an EES-Module, configured and arranged to provide CNS-Stimulation to a patient, and/or a PNS-Stimulation Module, especially an FES-Module, configured and arranged to provide PNS-Stimulation to a patient, a controller configured and arranged to control the CNS-Stimulation Module and/or the PNS-Stimulation Module, and at least one sensor configured and arranged to measure at least one parameter indicative of the movement of at least one limb and/or part of a limb of a patient.

A device for transcutaneous electrical stimulation is provided. The device comprises circuitry configured to generate transcutaneous stimulation signals. The device also comprises a first signal output component for electrically connecting to a first electrode connector to deliver generated transcutaneous stimulation signals. The first signal output component comprises a first four-pole electrical connector part. The device further comprises a second signal output component for electrically connecting to a second electrode connector to deliver generated transcutaneous stimulation signals. The second signal output component comprises a second four-pole electrical connector part. The device further comprises a controller to selectively control output of the stimulation signals to selected pairs of poles across the first and second four-pole electrical connector parts. Each selected pair of poles comprises one pole from the first four-pole electrical connector part and one pole from the second four-pole electrical connector part.