This invention is a device that provides feedback controlled pressure output that delivers a highly controlled and accurate air stimulus into the larynx for diagnostic use. The device is designed to be significantly more accurate, safer for the patient, and highly modular for easy future modifications compared to previously available commercial devices.

A method for evaluating hearing of a user comprising: generating a baseline hearing profile for the user comprising a set of gain values based on a volume setting, each gain value in the set of gain values corresponding to a frequency band in a set of frequency bands; accessing a soundbite comprising a phrase characterized by a frequency spectrum predominantly within one frequency band; playing the soundbite amplified by a first gain in the frequency band; playing the soundbite amplified by a second gain in the frequency band; receiving a preference input representing a preference of the user from amongst the soundbite amplified by the first gain and the soundbite amplified by the second; and modifying a gain value, corresponding to the frequency band, in the baseline hearing profile based on the preference input to generate a refined hearing profile compensating for hearing deficiency of the user.

A system for monitoring neural activity of a living subject is provided. The system may comprise a correspondence module configured to be in communication with (1) a neural module and (2) one or more additional modules comprising a sensing module, another neural module, and/or a data storage module. The neural module(s) are configured to collect neural data indicative of perceptions experienced by the living subject. The sensing module may be configured to collect (1) sensor data indicative of real-world information about an environment around the living subject, and/or (2) sensor data indicative of a physical state or physiological state of the living subject. The data storage module may be configured to store prior neural data and/or prior sensor data. The correspondence module may be configured to measure a correspondence (a) between the neural data collected by the neural module(s) and the sensor data collected by the sensing module, (b) between the neural data collected by two or more neural modules, and/or (c) between the neural data collected by the neural module(s) and the prior data stored in data storage module. The measured correspondence can be used to determine a presence, absence, or extent of a potential cognitive or physiological disturbance of the living subject.

A device for providing tactile stimulation of a subject via a pulse of compressible fluid, typically for medical diagnostic and therapeutic applications. The device preferably includes a high pressure fluid source and a low pressure fluid source. A pressure valve selectively connects the pressure sources to an outlet conduit. The outlet conduit includes an applicator for directing pulses against the skin of a subject. The pulses may be applied via one applicator or a plurality of applicators, and may be applied in one pattern or several patterns at various application sites. A method of providing tactile stimulation is also disclosed.

An apparatus for performing chemosensory disorder testing includes an application for installation on a mobile computing device. The application includes a set of instructions to receive a scanning signal from a scanner communicating with the mobile computing device, the scanning signal including a unique identifier. The application next identifies a predetermined scent responsive to the scanning signal. The application generates multiple choice display for display on a display screen associated with the mobile computing device, the multiple-choice display includes an indication associated with the identified predetermined scent and at least one indication associated with another scent. The application receives a test response input from the display screen responsive to an input from a test subject attempting to detect the predetermined scent.

An apparatus for performing chemosensory disorder testing includes an application for installation on a mobile computing device. The application includes a set of instructions to receive a scanning signal from a scanner communicating with the mobile computing device, the scanning signal including a unique identifier. The application next identifies a predetermined scent responsive to the scanning signal. The application generates multiple choice display for display on a display screen associated with the mobile computing device, the multiple-choice display includes an indication associated with the identified predetermined scent and at least one indication associated with another scent. The application receives a test response input from the display screen responsive to an input from a test subject attempting to detect the predetermined scent.

In an aspect of the invention, a method of identifying sensory inputs affecting working memory load of an individual is provided. The method comprises monitoring (S101) working memory load of the individual using a sensor device, detecting (S102) an increase in the working memory load of the individual, and identifying (S103), in response to the detected increase, at least one sensory input affecting the working memory load of the individual.

The invention discloses an objective and quantitative detection method for amblyopia by electroencephalogram (EEG). The method comprises the following steps: firstly, carry out binocular dichoptic viewing display, then design a visual evoked stimulation paradigm, establish a brain-computer interface platform, build a test interaction interface, next determine an amblyopia EEG quantitative index. By using a suppression coefficient (SI) to describe the binocular suppression relationship, quantify the degree of amblyopia, and finally obtain amblyopia detection result feedback, where the computer interaction interface module presents a final amblyopia detection result to realize feedback of a user. The operation is simple and rapid, the applicability is high, and the indexes are objective and quantitative.

An apparatus (1) is configured to perform a test procedure for measuring vibrotactile perception of a human subject. The apparatus (1) comprises a vibration probe (5) with an end portion (5A) arranged for engagement by a body part (100), a contactless temperature sensor (13) arranged to face the body part (100) when engaged with the end portion (5 A), and a force sensor (7) coupled to the vibration probe (5). A control unit (10) prepares for the test procedure by computing, as a function of a first output signal (T.sub.IR) of the contactless temperature sensor (13) and/or a second output signal (f) of the force sensor (7), one or more characteristic parameters indicative of presence or absence of the body part (100). When presence of the body part (100) is indicated by the one or more characteristic parameters, the control unit (10) sets a current temperature of the body part (100) to a current temperature value given by the first output signal (T.sub.IR).

In an aspect of the invention, a method of identifying sensory inputs affecting working memory load of an individual is provided. The method comprises monitoring (S101) working memory load of the individual using a sensor device, detecting (S102) an increase in the working memory load of the individual, and identifying (S103), in response to the detected increase, at least one sensory input affecting the working memory load of the individual.