A method of using an ankle exoskeleton device is provided herein. The method includes collecting one or more biomechanical data points from an individual. The method also includes developing individualized musculoskeletal simulations based on the one or more biomechanical data points. In addition, the method includes creating predictive simulations by modeling effects of an ankle exoskeleton device on the individualized musculoskeletal simulations. The method also includes utilizing established device-user relationships with real-time measurements to adjust device control. Lastly, the method includes optimizing design and control parameters of the exoskeleton device based on the predictive simulations and user responses.

A prosthetic foot cover device is described. The prosthetic foot cover may include a lattice framework formed to resemble a human foot. The lattice framework has a plurality of lattice cells to form the lattice framework. The prosthetic foot cover may have an inner cavity formed in the lattice framework which is sized and shaped to contain a prosthetic foot, and the inner cavity has an opening to receive the prosthetic foot. The prosthetic foot may have a foot pad that is an outer membrane layer and is joined with a portion of the lattice framework to support a portion of the lattice foot framework.

A prosthetic foot cover device with a pressure chamber is described. The prosthetic foot cover may include a lattice framework formed to replace a human foot. An open cavity may be formed in the lattice framework, which is sized and shaped to contain a prosthetic foot. A pressure chamber may be disposed in the lattice framework. A first one-way check valve is provided for the pressure chamber to allow air to be expelled from the pressure chamber and to generate a negative pressure within the pressure chamber as an amputee uses the prosthetic foot and the lattice framework. A remnant limb socket may be connected to the pressure chamber. A negative pressure may be developed in the remnant limb socket as air is pulled from the remnant limb socket into the pressure chamber. A method for additive manufacture of a prosthetic foot cover device is also described.

A method of using an ankle exoskeleton device is provided herein. The method includes collecting one or more biomechanical data points from an individual. The method also includes developing individualized musculoskeletal simulations based on the one or more biomechanical data points. In addition, the method includes creating predictive simulations by modeling effects of an ankle exoskeleton device on the individualized musculoskeletal simulations. The method also includes utilizing established device-user relationships with real-time measurements to adjust device control. Lastly, the method includes optimizing design parameters of the exoskeleton device based on the predictive simulations and user responses.

A blood flow stimulating device including a boot including a sole and an upper; a sock disposed within the boot; and a bladder disposed within or on the sock, wherein the bladder is configured to undergo repeated inflation and deflation so as to stimulate blood flow in a wearer of the blood flow stimulating device, wherein the sock further includes a toe region, a heel region and a raised portion between the toe region and the heel region that, in use, reduces the distance between the sock and a foot of a wearer of the blood flow stimulating device at the raised portion of the sock.

A prosthesis system having at least two sensors, at least one control device, which is coupled to the sensors and processes sensor signals of the sensors, at least one actuator, which is coupled to the control device and can be activated or deactivated on the basis of control signals of the control device, and at least one movably mounted prosthesis component, which can be displaced by the actuator. A standard program, which assigns an actuator action to each sensor independently of the duration and/or intensity of the sensor signal, is stored in the control device or can be called up by the control device.

Exosuit systems and methods according to various embodiments are described herein. The exosuit system can be a suit that is worn by a wearer on the outside of his or her body. It may be worn under the wearer's normal clothing, over their clothing, between layers of clothing, or may be the wearer's primary clothing itself. The exosuit may be assistive, as it physically assists the wearer in performing particular activities, or can provide other functionality such as communication to the wearer through physical expressions to the body, engagement of the environment, or capturing of information from the wearer. One or more patch assemblies may be removably coupled to the exosuit.

A miniaturized monitoring device can include electronic circuitry, housing, and communications protocols. The device can be a robust sensing device that can quantify electrolyte content accurately and transmit continuously from within fecal effluent or urine, or other human bodily fluid and/or solid samples. The device can be fully immersed in the testing sample, which can be in a container, an ostomy bag, or otherwise.

Rehabilitating an impaired body part of a subject such as a stroke patient includes systems, devices, and methods using an orthosis system configured to attach to the impaired body part and to move or assist in movement of the impaired body part. A control system is configured to operate the orthosis system in a mode in which the orthosis system first allows the subject to move volitionally or attempt to move volitionally the impaired body part in a predefined motion and then operates to move or assist in the predefined motion of the impaired body part. Additional modes of operation include a brain computer interface mode of operation and a mode in which the orthosis system operates in a continuous passive mode of operation comprising a plurality of repetitions of an exercise to move the impaired body part.

An orthosis device for a subject includes a main housing assembly configured to be worn on an upper extremity of the subject, and a body part interface assembly configured to be secured to the portion of the upper extremity and induce, as actuated by a motor mechanism, flexion and extension motion of the secured body part. A flexible intermediate member is interposed between the main housing assembly and the body part interface assembly, and is configured to flex or extend responsive to actuation by the motor mechanism to cause the body part interface assembly to flex or extend the secured body part.