A mobile apparatus includes a motion action portion. The motion action portion including a frame portion, at least part of the frame portion including a structural battery, the structural battery including one or more energy storage devices. Each of the one or more energy storage devices having at least one anode core of a continuous carbon fiber, an electrolyte arranged on the at least one continuous carbon fiber core, and a cathode layer arranged to the at least one continuous carbon fiber core on the electrolyte, and at least one interface electrically connected to the structural battery, the interface for inputting power for charging the structural battery and for outputting power.

Vibration based stimulation or pressure based stimulation are commonly employed in a wide range of devices for medical, therapeutic, and recreational activities. These are designed to be applied against a predetermined region of a user's body. However, there are many instances where it would beneficial to provide the user with a “wearable” device where these one or more predetermined regions of the user's body may be inserted through or disposed within the device providing vibratory and/or pressure based stimulation. Further, such devices may be augmented with other therapeutic means such as light therapy or ultrasonic therapy. Accordingly, a range of wearable devices exploiting hollow shaft motors, electromagnetic actuators, and fluidics are presented.

A computer-implemented system may include an electromechanical machine configured to be manipulated by a user while the user performs a treatment plan, an interface comprising a display configured to present information associated with the treatment plan, and a processing device configured to receive, from one or more data sources, information associated with the user, wherein the information comprises one or more risk factors associated with a cardiac condition or a cardiac outcome, generate, using one or more trained machine learning models, the treatment plan for the user, wherein the treatment plan is generated based on the information associated with the user, and the treatment plan comprises one or more exercises associated with managing the one or more risk factors in order to reduce a probability of a cardiac intervention for the user, and transmit the treatment plan to cause the electromechanical machine to implement the one or more exercises.

A gait evaluation apparatus that evaluates a training gait of a paralyzed patient suffering from paralysis in a leg includes an acquisition unit configured to acquire a plurality of motion amounts of a paralyzed body portion according to a gait motion and an evaluation unit configured to evaluate that the gait motion is an abnormal gait in a case where at least one of the motion amounts acquired by the acquisition unit meets any one of a plurality of abnormal gait criteria set in advance. The abnormal gait criteria include at least two or more first criteria, which are criteria relevant to motion amounts of different parts of the paralyzed body portion, or at least two or more second criteria, which are criteria relevant to motion amounts of the same part of the paralyzed body portion in different directions.

A massage roller assembly that includes an outer roller surface and a plurality of vibration motors positioned adjacent to the outer roller surface that are configured to transmit vibrations to the outer roller surface. The vibration motors are individually controllable such that at least first and second sets of vibration motors can be switched on and off individually.

A system for facilitating resuscitation includes: a first electrode assembly having a therapy side and a first motion sensor; a second electrode assembly having a therapy side and a second motion sensor; processing circuitry operatively connected to and programmed to receive and process signals from the first and second motion sensors to estimate at least one of a chest compression depth and rate during administration of chest compressions and to compare the chest compression depth or rate to a desired range; and an output device for providing instructions to a user to administer chest compressions based on the comparison of the estimated chest compression depth or rate to the desired range. One or both of the electrode assemblies may be constructed so that the conductive therapeutic portion is able to maintain substantial conformance to the anatomy of the patient when coupled thereto. For example, at least a portion of the flexible electrode pad may be able to flex from a more rigid sensor housing, or the sensor housing itself may be relatively small compared to the flexible electrode pad so as not to cause lift off of the therapeutic side from the patient.

A spinal therapy apparatus includes one or more manipulating assemblies. In some examples a first manipulating member is arranged to engage a spine at a first vertebral area between a spinous process and a transverse process on a first side of a spine and a second manipulating member is arranged to engage the spine at a second vertebral area between a spinous process and a transverse process on the first side of the spine. The first and second manipulating members are coupled together at their proximal ends to permit the first and second manipulating members to be driven simultaneously and the coupling permits motion of the first and second manipulating members relative to one another in an axial direction. In other examples a drive system is adapted to drive first and second manipulating members simultaneously and independently. The disclosure also relates to a spinal therapy bed including such manipulating assemblies and methods of using and training spinal therapy devices.

A stimulator substrate device for stimulating nerve cells, and apparatus including same, in particular nerve cells in an extremity, includes a substrate support, in which a plurality of stimulators for emitting stimulation signals to the nerve cells are provided. The plurality of stimulators is provided in a line on the substrate support and the substrate support is tubular.

A visual assistance system or distance and location detection system is provided. The system comprises a sensor detecting distance of objects in a user's path and alerting the user when an object is within a designated proximity to the user. The system further comprises a location detection system using GPS technology that tracks the user's location and issues an alert to the user or other individual when the user's location exceeds the boundaries of a designated safe zone.

A method for optimizing at least one exercise. An exercise apparatus is configured to enable a user to perform the at least one exercise. The method includes receiving user data. The method includes generating, based on the user data, initial target data. The method includes receiving measurement data associated with one or more sensors. The method includes determining, differential data. The determining is based on one or more differences between the initial target data and the measurement data. The method includes receiving cohort data. The method includes generating, via an artificial intelligence engine and based on the differential data, a machine learning model trained to generate message data based on a difference between the differential data and the cohort data. The method includes transmitting, to an interface associated with a user, a message to the user based on the message data.