An electrode sheet is capable of suppressing an influence of noise that is applied on a wire, and a biological signal measuring device uses the electrode sheet. The electrode sheet is provided with a sheet, a biological signal receiving electrode formed at the sheet and exposed from the sheet, a biological signal amplifier formed at the sheet, an interface part for connection to an external biological signal processing unit, a first wire that connects the biological signal receiving electrode and an input part of the biological signal amplifier to each other, and a second wire that connects the interface part and an output part of the biological signal amplifier to each other.

The present disclosure provides systems, apparatuses, and methods for use of wearable electrode assemblies. The electrode assemblies improve comfort by providing increased overall surface area of their bottom surfaces, which make contact with the patient's scalp and hair. Collapse, compression, or telescoping of the bottom surface will thereby decrease the direct force and/or pressure applied by the distal member or members of the bottom surfaces to the skin. This may be advantageous in patients who have little to no hair in electrode contact areas, patient populations that are particularly skin-sensitive, and/or patients which must wear the electrode assemblies of an extended time period. The electrode assemblies further include structures to dispense and/or maintain conductive gel placed over the patient's skin, thereby maintaining electrical connection quality, and/or to facilitate the clearing of skin and/or hair prior to establishing an electrical connection.

There is provided a sensor for an electroencephalographic (EEC) device for measuring electrical signals generated by the neuronal activity of a subject. The sensor has at least one blade-like contact surface and the contact surface has a curved profile adapted for user comfort and electrical contact.

A method of updating a protocol for a Virtual Reality (VR) medical test via a user device having a processor, the VR medical test being performed on a subject via a VR device worn by the subject, wherein the method is performed by the processor and the method comprises: displaying GUI elements associated with the protocol on the user device, the GUI elements having user adjustable settings for modifying a functioning of the VR medical test; receiving a selection input from the user device corresponding to a selection of the GUI elements; receiving a setting input from the user device that corresponds to the selected GUI elements; modifying the user adjustable setting for each of the selected GUI elements according to the corresponding setting input; and updating the protocol based on the user adjustable setting for each of the selected GUI elements and operations associated with the VR device.

A head coil assembly includes a housing with a lower portion, an upper portion, a left portion, and a right portion, wherein each portion includes two or more radio-frequency (RF) coils, wherein the portions are sized and shaped to adjustably conform to a curvature of the subject's head for magnetic resonance (MR) imaging of the subject's head placed inside the housing, wherein the portions are operable to transition from an open position where the portions are sufficiently apart from each other to a closed position where the portions are adjusted to tighten a wrap around the subject's head along the curvature, and wherein the two or more RF coils in each portion are disposed in such manner that when the portions are operated to transition from the open position to the closed position, the RF coils of each portion remain decoupled to each other even along edges of each portion.

The source light having a range of optical wavelengths is split into sample light and reference light. The sample light is delivered into a sample, such that the sample light is scattered by the sample, resulting in signal light that exits the sample. The signal light and the reference light are combined into an interference light pattern having optical modes having oscillation frequency components respectively corresponding to optical pathlengths extending through the sample. Different sets of the optical modes of the interference light pattern are respectively detected, and high-bandwidth analog signals representative of the optical modes of the interference light pattern are output. The high-bandwidth analog signals are parallel processed, and mid-bandwidth digital signals are output. The mid-bandwidth digital signals are processed over an i number of iterations, and a plurality of low-bandwidth digital signals are output on the ith iteration. The sample is analyzed based on the low-bandwidth digital signals.

Apparatus is provided that includes left-nostril, right-nostril, and oral pressure sensors and oral pressure probes. A memory is configured to store left-nostril, right-nostril, and oral pressures sensed by the respective sensors, over a total period of at least 12 hours. A processor is configured to convert the left-nostril, right-nostril, and oral pressures stored in the memory to left-nostril, right-nostril, and oral pressure airflows, respectively, and calculate a series of orally-weighted laterality-indices over a respective series of sub-periods of the total period. Each of the orally-weighted laterality-indices of each of the sub-periods is indicative of a laterality index over the sub-period weighted by a normalized oral airflow over the sub-period, such that the greater the normalized oral airflow, the smaller the orally-weighted laterality-index. Each of the orally-weighted laterality-indices of each of the sub-periods reflects relative airflow through the left and the right nostrils over the sub-period. Other embodiments are also described.

A method for obtaining a near-infrared spectroscopy (fNIRS) cerebral signal in a subject includes: placing a near-infrared emitter and respective proximal and distal near-infrared detectors on a skin of a head of a subject; during a baseline recording stage with the subject in resting-state, record near-infrared signals, the recorded signals including a baseline deep-signal and a baseline shallow-signal; calculate a scaling factor between amplitudes of the baseline deep-signal and the baseline shallow-signal at a given task-frequency; with the subject undergoing a cyclic cerebral stimulation at the task-frequency during a stimulation recording stage, record near-infrared signals, the recorded signals comprising a shallow-signal and a deep-signal; and applying the scaling factor to the shallow-signal, calculating the cerebral signal at the task-frequency as a difference between the deep-signal and the scaled shallow-signal, at the task-frequency.

An apparatus for measuring patient data includes a frame having a plurality of electrode hubs. Each hub can include one or more electrode members. The frame can be configured to receive a head of a patient. Each of the electrode hubs can have a single electrode member or a plurality of electrode members that extend from or are connected to an outer member for contacting a scalp of the head of the patient. The outer member can have at least one circuit configured to transmit data received by at least one of the electrode members to a measurement device via a wireless communication connection (e.g. Bluetooth, near field communication, etc.) or a wired communication connection.

In described embodiments, a device and method for diagnosing brain and neurological issues is provided. The device measures the performance of Convergence, Divergence, and binocular tracking capabilities of a subject's eyes, which can be used to determine whether a subject has experienced a brain or other neurological event.