Methods, systems, and computer programs encoded on a computer storage medium, for improving EEG measurements by identifying artifacts present in EEG measurements and providing a real-time indication to a user of likely artifacts in EEG measurements are described. EEG measurements of a patient can be obtained by placing a wearable device or EEG cap on a patient's head. Sensors in the cap provide EEG data to a computing device that processes the data to identify one or more artifacts in the EEG data. The artifacts can be identified by conducting one or more operations of determining the signal to noise ratio of the line noise, calculating mutual information between sensor pairs, and applying the p-welch method. Based on the types of artifacts identified, the computing device can output an indicator that provides feedback to the technician performing an EEG test to make adjustments to the test setup.

An active implantable stimulating device (10) includes: (a) a tissue coupling unit (40) for being implanted directly onto a vagus nerve (Vn) of a patient, (b) an EEG-unit (70) for measuring an electroencephalogram of the patient, (c) an encapsulation unit (50) configured for being subcutaneously implanted, (d) an energy transfer lead (30) for transferring pulses of electrical and/or optical energy, (e) a signal transfer lead (60) for transferring signals between the EEG unit and the encapsulation unit. EEG electrodes (70a-70d) monitor the electric activity of the brain of a patient. The EEG signal is conveyed to the electronic circuit (53) in the form of EEG conditioned data. The electronic circuit analyses the EEG conditioned data to yield analysis results. The electronic circuit takes a decision to trigger energy pulses to stimulate the vagus nerve (VN).

An inductive sensing system (8) is for detecting bleeding (e.g. blood pools) in one or more regions of the body. The system comprises a resonator circuit (10) having at least one antenna (12) which is driven with an oscillatory drive signal to cause generation of electromagnetic signals for application to a body. The signals induce eddy currents in the body which generate secondary EM signals returned from the body. These interact with the resonator circuit by adding an additional component of inductance to the circuit. This inductance component varies depending upon the conductivity of the fluid in which the eddy current is induced. Blood has a different conductivity to other body fluids. The system is configured to detect presence of abnormal accumulations of blood based on the additional inductance component. The system generates a data output representative of the determination.

An electroencephalography net (44) comprised of electrodes (34, 36) coupled together by a connector (28) comprising separate elastically (32) and plastically (30) deformable elements.

A universal respiratory detector for detecting a respiratory gas. The universal respiratory detector may include a plurality of layers with a visual indicator to quickly and reversibly change color to detect a respiratory gas parameter such as carbon dioxide. The color change may be visible from both sides of the detector. In some examples, the respiratory detector may be a biocompatible and conformable sticker for mounting on a person's face or an oxygen delivery device.

A system includes: a light source that emits pulsed light that illuminates a user's head portion; a photodetector that detects at least part of pulsed light returning from the head portion and that outputs one or more signals corresponding to an intensity of the at least part; electrical circuitry; and a memory that stores an emotion model indicating a relationship between the one or more signals and emotions. Based on a change in the one or more signals, the electrical circuitry selects an emotion by referring to the model. The one or more signals include a first signal corresponding to an intensity of first part of the reflection pulsed light and a second signal corresponding to an intensity of second part of the reflection pulsed light. The first part includes part before a falling period is started; and the second part includes at least part in the falling period.

A method for estimating an ear geometry of an ear of a user with a hearing device, the hearing device comprising an ear canal microphone, an external microphone, and a receiver, includes: obtaining an external input signal using the external microphone; providing an output signal by the receiver; obtaining an ear canal microphone input signal using the ear canal microphone; and estimating the ear geometry based on the external input signal and the ear canal microphone input signal.

Improved assessment of brain injuries, and improved brain injury management, is achieved using a combination of impact-related data derived from instrumented mouthguard devices, human function performance testing, and biomarkers derived from biological fluid (such as saliva and/or blood). The human function performance testing may include brain function performance testing, and/or other forms of human function performance testing. This involves combining a data-driven understanding of a head impact event (based on data collected via an instrumented mouthguard device) with a data-driven understanding of human function performance following that head impact event. The biomarkers may include salivary mRNA and/or ncRNA, and/or blood proteins (for example via a FDA-approved Brain Trauma Indicator test).

The disclosed biopotential measurement device may include a front end comprising a biopotential measurement sensor and a back end comprising a processor programmed to process biopotential signals detected by the biopotential measurement sensor. The biopotential measurement device may also include an isolation circuit that, during at least a sampling phase of the biopotential measurement sensor, electrically isolates the front end from the back end. Various other methods, systems, and computer-readable media are also disclosed.

Apparatus for applying Transcranial Magnetic Stimulation (TMS) to an individual, wherein the apparatus comprises: a head mount for disposition on the head of an individual; and a plurality of magnet assemblies for releasable mounting on the head mount, wherein each of the magnet assemblies comprises a permanent magnet, and at least one of (i) a movement mechanism for moving the permanent magnet and/or (ii) a magnetic shield shutter mechanism, for selectively providing a rapidly changing magnetic field capable of inducing weak electric currents in the brain of an individual so as to modify the natural electrical activity of the brain of the individual; wherein the number of magnet assemblies mounted on the head mount, their individual positioning on the head mount, and their selective provision of a rapidly changing magnetic field is selected so as to allow the spatial, strength and temporal characteristics of the magnetic field to be custom tailored for each individual, whereby to provide individual-specific TMS therapy, to assist in diagnosis or to map out brain function in neuroscience research.