313 results about "Test subject" patented technology

The technology of active noise reduction (ANR) is incorporated into audiometry testing in a variety of formats. Analog feedback, digital feedback, adaptive feedforward, and adaptive feedback noise control schemes are presented for use in audiometry to reduce the ambient noise heard by the test subject, allowing subject testing in higher ambient noise fields. Audiometer test signals are appropriately compensated so the test results are accurate and comply with existing calibration standards for audiometers. Existing audiometry headphone technologies are modified so that ANR can be accomplished while satisfying existing standards for audiometric testing. Embodiments are also defined for alternate headphone arrangements that may not conform to current (1997) audiometric testing standards but provide sufficient performance advantages to warrant new standards for audiometry testing in the future.

In a portable biological information monitor apparatus, a pulse wave detection signal obtained by light emission from a green LED and a body motion detection signal obtained by light emission from an infrared LED are detected as biological information. This biological information is analyzed to compute various barometers. In a wake normal mode of a set generation mode, body motion and pulse are calculated as wake evaluation barometers for evaluation of a test subject's status in wake. In a wake steady state motion mode, body motion, pulse, and pitch are calculated as motion evaluation barometers for evaluation of the test subject's status in steady state motion. In a sleep mode, body motion, pulse, and autonomic nervous function are calculated as sleep evaluation barometers for evaluation of the test subject's status in sleep. Necessary barometers are thereby generated regardless of the test subject's action using the portable monitor apparatus alone.

The present invention relates to a system for the 3-D monitoring and analysis of motion-related behavior of test subjects. The system comprises an actual camera, at least one virtual camera, a computer connected to the actual camera and the computer is preferably installed with software capable of capturing the stereo images associated with the 3-D motion-related behavior of test subjects as well as processing these acquired image frames for the 3-D motion parameters of the subjects. The system of the invention comprises hardware components as well as software components. The hardware components preferably comprise a hardware setup or configuration, a hardware-based noise elimination component, an automatic calibration device component, and a lab animal container component. The software components preferably comprise a software-based noise elimination component, a basic calibration component, an extended calibration component, a linear epipolar structure derivation component, a non-linear epipolar structure derivation component, an image segmentation component, an image correspondence detection component, a 3-D motion tracking component, a software-based target identification and tagging component, a 3-D reconstruction component, and a data post-processing component In a particularly preferred embodiment, the actual camera is a digital video camera, the virtual camera is the reflection of the actual camera in a planar reflective mirror. Therefore, the preferred system is a catadioptric stereo computer vision system.

A device for monitoring a test subject includes a light source and at least one optical waveguide configured for at least one of directing light from the light source onto a biological substrate and receiving the light directed onto the biological substrate. The device also includes a sensor operable to detect the light received, a logic component operable to analyze the light detected by the sensor, an output component operable to convey information from the logic component to a user of the device, and a housing containing the light source, the sensor, the logic component, and the output component, where the at least one optical waveguide forms at least one bristle extending outside of the housing.

A method for adaptively determining a model of visual performance of a test subject comprising the step of exposing a test subject to a plurality of trials. Each trial comprises the steps of identifying the stimulus pattern to test, generating a stimulus pattern on a display, determining whether the stimulus pattern generated an OKR, updating the model to incorporate the OKR results, and determining whether the updated model is acceptable. The trials can be iteratively repeated until the model for visual performance is acceptable.

The present invention is an enzymatic method and diagnostic kits for detecting and quantifying the presence of one or more lysophospholids in a sample of bodily fluid taken from a test subject. The method uses enzymes in a two step assay and may be used to detect disease conditions associated with altered levels of lysophospholipids and to correlate such conditions with altered levels of lysophospholipids.

The invention provides a multiparametric method of assessing the reaction of a patient's immune system to a test subject. The invention compares a patient sample reacted with a test sample and a third party sample and combines the assessments of the multiple parameters to correlate the test reaction with a clinical event.

A method for identifying a test subject being tested for consumption of a selected substance includes storing in a database of a facial recognition processing system a gallery of facial images of a set of individuals. The facial recognition processing system receives a facial image of a test subject being tested for consumption of the selected substance and compares the received facial image with at least some of the facial images in the stored gallery by executing a facial recognition algorithm. In response to a match between a facial image in the stored gallery and the received facial image having a predetermined level of match certainty; the facial recognition processing system identifies the test subject. In response to a failure to obtain a match between a facial image in the stored gallery and the received facial image having a predetermined level of match certainty, the facial recognition processing system flags the received facial image for subsequent manual analysis.

A one-camera, binocular, video-oculography (1CBVOG) system for measuring the movement of both of the eyes of a test subject, while the head of the test subject is undergoing a period of vestibular or oculomotor stimulation, includes: (a) a base frame, (b) a binocular imaging component, including a video camera adapted to capture a sequence of images containing both of the eyes of the test subject, (c) an optical component, (d) an illumination source, (e) a sensor module that senses translational and rotational motion of the head along and about three, mutually orthogonal axes that approximately align with the axes of the inner ears' semicircular canals, and (f) a computing device configured to quantify and measure the movement of the test subject's eyes from the sequence of captured images.

A participant is evaluated to determine compatibility among different military disciplines. The participant is first subjected to physical, physiological, and psychological tests. The results of tests are compared with a database that contains the results of the same tests subjected to a set of elite military members from different military disciplines. At least one specific military discipline compatible with the participant based on the comparison is identified. A list of identified specific disciplines from most compatible to least compatible associated with a corresponding match score is then generated.

The present invention discloses a machine learning-based method for evaluating and predicting ASD, comprising the following steps: S1. data collection: using an eye tracker to separately collect eye movement data that an eye ball scans a human face when persons participating in a test watch a human face image, wherein the persons participating in the test comprise individuals who have ASD and normal individuals; S2. feature extraction: dividing the human face image into different areas according to collected eye movement coordinate data, extracting a feature from the original data collected by the eye tracker, and making a mark; S3. classifier training: training a classifier by using a marked feature, to obtain a classifier model for predicting ASD; and S4. prediction: testing on a test subject by using the classifier model for predicting ASD acquired in step S3, to evaluate and predict severity of autism of the test subject. The present invention may be considered as a supplementary method of ASD evaluation, so that ASD evaluation and prediction in an early stage is more accurate and convenient.

Systems and methods are provided for determining pre-cognitive and/or cognitive emotional response to predetermined olfactory stimuli. Among other things, the invention may include exposing a test subject to a controlled flow of a predetermined olfactory stimulus, measuring eye data (e.g., using an eye tracking device) corresponding to when the olfactory stimulus reached the subject's nose, and analyzing and processing the eye data for determining the subject's emotional response to the olfactory stimulus. In some implementations, the invention may include measuring the test subject's respiratory parameters so as to deliver the predetermined olfactory stimulus at a certain point in the test subjects respiratory cycle.

The invention discloses a sleep quality judging method and a sleep instrument. The method comprises the following steps: according to the sleep stage of a tested subject, determining a sleep structure score of the tested subject; according to the sleep state of the tested subject, determining a sleep state score of the tested subject; according to the sleep habit of the tested subject, determining a sleep habit score of the tested subject; according to the sleep environment of the tested subject, determining a sleep environment score of the tested subject; according to one or more of the sleep structure score, the sleep state score, the sleep habit score and the sleep environment score, calculating a sleep quality score of the tested subject; and according to the sleep quality score, determining the sleep quality of the tested subject.

The invention relates to methods for diagnosing or monitoring psychotic disorders such as schizophrenic or bipolar disorders, comprising measuring the level of one or more biomarker(s) present in a cerebrospinal fluid sample taken from a test subject, said biomarker(s) being selected from the group consisting of: glucose, lactate, acetate species and pH. The invention also relates to methods of diagnosing or monitoring a psychotic disorder in a subject comprising providing a test sample of CSF from the subject, performing spectral analysis on said CSF test sample to provide one or more spectra, and, comparing the one or more spectra with one or more control spectra. The invention also relates to sensors, biosensors, multi-analyte panels, arrays, assays and kits for performing methods of the invention.

A system and method for automated assessment of constrained constructed responses provides for automatic, e.g., programmatic, assessing of a test subject response to a constrained constructed response item or question. In one embodiment, paper test materials with test subject markings thereon are converted to electronic form. Test subject markings are further isolated, for example, by registration, sizing and removal of markings other than a graphic response. The subject markings are further compared with a baseline response, correctness deviation criteria and incorrectness deviation criteria (e.g., correctness, incorrectness, substantial correctness, substantial incorrectness, and so on) from which one or more of a score, further learning or other assessment results may be determined. Cluster analysis or other post-evaluation or post-assessment processing may also be conducted, or re-evaluation or re-assessment may also be conducted.

Systems and methods for providing improved techniques for evaluating performance of intraocular lenses. Such techniques can be used to evaluate lens designs and can help reduce the need for multiple clinical trials that may otherwise be needed to evaluate multiple design iterations. In one embodiment, a method is provided for method for evaluating performance of an intraocular lens, where the method comprises capturing a plurality of images through the intraocular lens at different focus positions; displaying at least one selected image from the plurality of images to a test subject; receiving input from the test subject indicative of perceived acuity of the at least one selected image; and determining a measure of intraocular lens performance from the received input.

A breathalyzer test device includes vigilance detecting means for detecting the vigilance of a test subject, and breathalyzer test means for performing a breathalyzer test on the subject based on the vigilance detected by the vigilance detecting means.

A hearing test device and method are disclosed which involve the placement of a testing probe in the ear canal of a test subject. The device analyzes responses to stimuli applied to the ear canal to determine whether the testing probe has been properly placed in the ear canal. The device may determine, for example, whether the probe is stable, whether it is sealed in the ear canal, whether the resulting volume of the ear canal is acceptable, and/or whether the stimuli delivery system is blocked in any way. If the device determines that the testing probe has been properly placed in the ear canal, the device automatically starts a hearing test without requiring any operator input.

A device has a measuring device, in particular an alcohol-measuring device (3), for measuring the state of intoxication of a test subject and for generating a corresponding measured value. A camera (5) is provided for recording an image with the face of the test subject. A control unit (4) is configured to store the measured value together with the image in a memory unit (10). An analyzer (12) is configured such that the analyzer can identify a face and/or a defined, fixed pattern in the image. A follow-up action is triggered by the analyzer (12) when a face and/or pattern could not be identified.

An ultrasonic diagnostic apparatus is provided for displaying a color map on which a difference in blood flow dynamics is reflected. Setting a test subject who is administered a contrast agent is assumed as an imaging target, and a probe transmits and receives ultrasonic waves to and from the target for contrast imaging. Image data is constructed based on signals received by the probe and a time-intensity curve is generated from intensity values of the image data. According to the time-intensity curve, a value of a predetermined parameter is calculated for producing a distribution image of blood flow dynamics. The distribution image (color map) of the blood flow dynamics is produced from the parameter value. The color map is a two-dimensional or a three-dimensional image being color-coded according to the parameter value. At least one of the followings may be used as the parameter; a contrast agent inflow start time, a balanced intensity arrival time, a contrast agent disappearance start time, a contrast agent duration, a preset threshold arrival time, an intensity increase rate, an intensity decrease rate, intensity of balanced state, and a total flow amount.

A Test and debug processor that can execute JTAG scans without the involvement of an external CPU or dedicated hardware. The processor includes a JTAG-bus controller logic, a JTAG port coupled to the JTAG-bus controller logic, memory capable of storing JTAG instructions, and an instruction decoding unit capable of fetching or requesting JTAG instructions from the memory. During use, the JTAG scan functions are encoded in instructions that are natively executable by the processor hardware without software interpretation. The instructions are then stored in a memory structure, fetched and executed directly by the processor. The instruction could optionally include the end-state of the bus after the operation, information about the bit count of the data to be scanned, information about the location of the data to be sent out of the JTAG port and also the location to store the received information from the test subject. Optionally, the test processor can directly access any memory location to fetch or store test data objects. This is achieved by adding a memory-bus interface to the processor allowing it to be the memory bus master. Also the test-processor can have the ability to decode and execute arithmetic and logic operation by adding an ALU the processor. The processor can also have the ability to execute register transfer operations to execute functions such as JUMP to control the run path.

A probe is disclosed, comprising a beam 4B, which has a front end 4b1, an intermediate portion 4b2 and a base end 4b3, the front end being a portion for contacting a test subject through a contactor, the base end being a portion for fixing the probe; and a substantially trapezoidal contactor 4A, which is fixed to the leading end 4b1 of the beam.

A vision testing system and method to assess vision function. In one embodiment, the vision testing system comprises: (1) a display; (2) a computer coupled to the display and configured to provide dynamic images, each including a substantially constant fixed point of fixation; and (3) a human input device coupled to the computer, wherein responses from a test subject are fed back to the computer to assess the test subject's vision function.

A portable sampling or testing device for pharmacokinetics and physiology studies and a method for using the device in conducting tests on stationary or moving animals, or human test subjects, is disclosed. The device includes an apparatus for conducting a test on a freely moving subject, or a device which may be moved by a technician to be positioned over an immobile subject, such as a premature infant or unconscious human subject in an intensive care ward. The device is designed and sized to be mobile. In one embodiment, the device comprises a wheeled cart which may be moved by a human test subject operably connected to it. In another embodiment, the device comprises a wheeled carriage positioned above an animal which wears a sling connected to the device. The device may include an uninterruptible power supply. The method provides for sampling bodily fluids or acquiring physiological readings from the test subject. The method provides for removal of body fluids with or without reintroduction of the withdrawn bodily fluids back into the freely moving subject.