An implantable device includes one or more electrodes to sense an electrical signal from a brain and a waveform analyzer to identify a half wave in the electrical signal; determine an amplitude and a duration of the half wave; determine if the amplitude satisfies a half wave amplitude criterion defined by a set of amplitude parameters comprising a minimum half wave amplitude and a maximum half wave amplitude; determine if the duration satisfies a half wave duration criterion defined by a set of duration parameters comprising a minimum half wave duration and a maximum half wave duration; and identify the half wave as a qualified half wave when the half wave amplitude criterion and the half wave duration criterion is satisfied. A neurological event may be detected based on one or more qualified half waves and electrical stimulation therapy may be delivered to the brain in response to the detection.

An electrode array for EEGs is described that includes a feedback amplifier driving one of the electrodes. Use of the feedback amplifier can eliminate the need to use precisely balanced resistors in a differential amplifier as well as allowing the elimination of a reference electrode and ground electrode.

This document discusses, among other things, systems and methods for managing pain of a subject. A system includes one or more physiological sensors configured to sense a physiological signal indicative of patient brain activity. The physiological signals may include an electroencephalography signal, a magnetoencephalography signal, or a brain-evoked potential. The system may extract from the brain activity signal one or more signal metrics indicative of strength or pattern of brain electromagnetic activity associated with pain, and generate a pain score using the one or more signal metrics. The pain score can be output to a patient or a process. The system may select an electrode configuration for pain-relief electrostimulation based on the pain score, and deliver a closed-loop pain therapy according to the selected electrode configuration.

An electrode padset and a method of using the electrode padset are disclosed herein. The electrode padset is a single unit, consisting of multiple patient-contacting conductive pads arranged on a single piece of material. The padset is comprised of a plurality of conductive pads, at least one conductive pad adapted to emit an electrical signal and at least one other conductive pad adapted to receive an electrical signal, and an electrically conductive material coupling the conductive pads.

In an embodiment a system for facilitating a subject's functional development includes sensing devices configured for sensing mind state signals; sensing devices configured for sensing body state signals; and a set of processing resources configured for generating a mind state indicator/measure, a body state indicator/measure, and a mind-body synergy indicator/measure that corresponds to an expected extent to which each of the subject's mind state and the subject's body state are cooperatively or synergistically aligned with respect to facilitating the subject's functional development. In an embodiment, the system can be configured for concurrently presenting a set of activities involving a model body part; engaging the subject in attempted imitation of the set of activities by way of attempted movement of a subject body part that is a mirror image of the model body part; presenting an indication of an expected extent to which each of the subject's mind state and body state are cooperative with respect to subject performance of the set of activities; and presenting an indication of an extent of subject relaxation. An associated multiple (e.g., up to 12) degree of freedom robotic orthosis can include a set of appendage motion modules configured for engaging with a portion of a subject appendage; a set of mechanical power interface modules coupled to the set of appendage motion modules and configured for facilitating movement of appendage motion modules within the set of appendage motion modules; and a set of flexible drive shafts couplable to the set of mechanical power interface modules.

A helmet includes a first sensor for detecting biological information of a wearer, a second sensor for detecting environment information around the wearer, and a controller configured to acquire the biological information and the environment information from the first sensor and the second sensor, respectively. The controller determines a cycle for executing detection by at least one of the first sensor and the second sensor, based on the biological information and the environment information.

A computer-based apparatus system for assessing, predicting, correcting, recovering, and reducing risk arising from an operator's deficient situation awareness (SA). This system identifies operator situation awareness by computer-apparatus and method that utilizes neurogenic-psychophysiological-neurocognitive-artificial intelligence processes. This system is configured to receive psychophysiological data from the operator via the neurogenic sensor(s) and configured to be loaded with data corresponding to the operator's baseline SA capacity and/or possesses AI algorithms to learn and calibrate the operator's baseline SA capacity and sound a warning in response if an SA deficiency threshold has been exceeded. Optionally, an autopilot/auto-driver/auto-operator/auto-worker/student alert/player & coach alert interface is configured to activate an autopilot/auto-driver/auto-operator/auto-worker command in response an SA deficiency threshold has been exceeded.

Disclosed are medical devices for sensing bioelectrical potential including an electroencephalography (EEG) headset, electrodes compatible therewith, and methods of operation thereof. The headset can comprise a left junction and a right junction, a plurality of length-adjustable bands connecting the left junction and the right junction, and a number of electrodes. Each of the electrodes can comprise an electrode body coupled to one of the plurality of length-adjustable bands and a detachable electrode tip configured to be detachably coupled to the electrode body. The electrode tip can comprise an electrode tip body, one or more deflectable electrode legs coupled to the electrode tip body, and a conductive cushioning material coupled to a segment of at least one of the one or more electrode legs. The conductive cushioning material can retain or be saturated with one or more conductors.

A hippocampal prosthesis for bypassing a damaged portion of a subject's hippocampus and restoring the subject's ability to form long-term memories. The hippocampal prosthesis includes a first set of hippocampal electrodes configured to receive an input signal from at least one of the subject's hippocampus or surrounding cortical region. The hippocampal prosthesis includes a processing device having a memory and one or more processors operatively coupled to the memory and to the first set of hippocampal electrodes. The processing device being configured to generate an output signal based on the input signal received from the first set of hippocampal electrodes. The hippocampal prosthesis includes a second set of hippocampal electrodes operatively coupled to the one or more processors and configured to receive and transmit the output signal to the subject's hippocampus.

A sensor array can be integrally defined in a fabric headgear. A gel distribution module can be connected to each sensor of the sensor array. Each module can include an outer part that is connectable to a second inner part so that the fabric of the headgear and sensor are between the inner and outer parts. Each module can be configured to facilitate the distribution of a gel onto a scalp of a patient and into contact with the sensor via actuation of an actuator of the module to permit rapid deployment of the gel at the sensor specific locations on the head of a patient. The gel can be distributed directly onto skin of the scalp even when the patient has hair at the sensor location. The sensor array can be positioned so that asymmetrical positioning of the sensors on a patient's head is detectable.