Abstract: An apparatus of the present technology generally includes an elongated shaft having a proximal portion and a distal portion, a first elongated channel extending from the proximal portion to the distal portion, a second channel extending from the proximal portion to the distal portion, and a slidable imaging probe disposed within the first elongated channel. The apparatus can be manually, robotically, and/or teleoperably steerable and is configured for delivery to a subject and/or positioning within a subject near or at a target location. Once the steerable apparatus has been successfully positioned at the target location, the imaging probe can be repositioned relative to the first elongated channel, thereby opening a working lumen. The working lumen and second channel are configured for removal of material from the target location within the subject by applying simultaneous activities including suction, irrigation, and/or deliver a tool to the target location.

Abstract: An insertion device includes: a tube having a first hole extending along a longitudinal axis of an insertion portion inserted into a subject and a second hole communicating with the first hole; and a frame member covering a periphery of an opening of the second hole formed on an outer peripheral surface of the tube, wherein the frame member includes a forceps channel which includes a first conduit including a first tubular path forming a first angle being an acute angle to the longitudinal axis, a second conduit including a second tubular path forming a second angle smaller than the first angle to the longitudinal axis, and an intermediate conduit including an intermediate tubular path, and the forceps channel includes a plurality of bent regions, and curvature centers of the plurality of bent regions are disposed in different directions with respect to the forceps channel.

Abstract: An ultrasound endoscope includes: a first rigid portion that is positioned at a front end of an insertion portion to be inserted inside a subject; a supporting portion that is connected to a proximal end of the first rigid portion and that has a long side along a longitudinal direction of the insertion portion; a second rigid portion that is connected to a proximal end of the supporting portion; an ultrasound transducer that is fixed to the supporting portion and that includes a plurality of piezoelectric elements arranged therein along the longitudinal direction of the insertion portion; a rotation mechanism configured to rotate the supporting portion and the ultrasound transducer in an integrated manner; and an angle display portion configured to indicate a state of the insertion portion corresponding to a rotation amount of the ultrasound transducer.

Abstract: An electronic endoscope and an electronic endoscope system, wherein the electronic endoscope comprises a tube body (100), at least two lenses (200) having a non-zero-degree viewing angle, an image sensing component (300), and a transmission module. The tube body (100) comprises a light receiving channel penetrating therein for sequentially accommodating the lenses (200), the image sensing component (300), and the transmission module. Optical axes of the lenses (200) are parallel to an extension axis of the light receiving channel. The image sensing component (300) receives images transmitted by the lenses (200) and converts the same into electrical signals. The transmission module drives the lenses (200) having a non-zero-degree viewing angle to rotate about the optical axes in the same direction. When the field-of-view region of the electronic endoscope changes, the field-of-view direction does not change.

Abstract: An in-body image capturing device (camera unit) with high reliability is suggested. A camera unit (11) includes an image capturing unit that includes a lens (26) and a first illumination unit (27a) and is capable of being introduced into a body. The first illumination unit (27a) and the image capturing unit are housed in a casing (22) that is integrally molded with an integral light-transmitting body (22x) and an integral light shielding body (22y).

Abstract: The endoscope system includes a light source unit, a light source controller, an image acquisition unit, a white balance unit, and a correction factor-calculating unit. The white balance unit multiplies a first image signal by a first gain factor, multiplies a second image signal by a second gain factor, and performs white balance processing using a corrected gain factor that is obtained through the correction of at least one of the first gain factor or the second gain factor.

Abstract: Described herein is a cleaning apparatus (10) for a medical device (12) having one or more internal channels. Further described is a method for cleaning the medical device using the cleaning apparatus. The cleaning apparatus includes at least two cleaning pumps (20) adapted to pump a viscoelastic liquid (22), each cleaning pump having individual flow control. Each cleaning pump is also fluidly connectable to one or more of the internal channels to allow the viscoelastic liquid to be pumped therethrough thereby removing contaminants.

Abstract: An endoscope (10) includes an endoscope shaft (13), with a distal shaft portion (20), a central shaft portion (30) and a proximal shaft portion (40), and a light admission face (11) at the distal shaft portion (20). A cross section of the central shaft portion (30) is smaller than the cross section of the distal shaft portion (20) and smaller than the cross section of the proximal shaft portion (40).

Abstract: An otoscope includes an instrument head, a tip element and an optical system. The instrument head has a distal insertion portion for insertion into an ear of a human or veterinary subject. The distal insertion portion has a distal opening. The tip element is releasably attached to the distal insertion portion. The tip element has a distal opening. The optical system is contained within the instrument head. The optical system includes a plurality of optical components. The optical system further comprises a viewing component for viewing of an image of a target of interest aligned along an optical axis disposed within said distal opening. The optical system is configured to provide a field of having a diameter equaling at least 7 mm at a distance of at least 15 mm from a distal opening of said attached tip element. The optical system is further configured to simultaneously provide a distance range of optimal focus having a range of at least 8 mm.

Abstract: A method for controlling the illumination of ophthalmological devices which operate in an observation mode and a recording mode. The method adapts the illuminance from ophthalmological devices which include an observation mode and a recording mode and the illuminance therefrom being increased above a specified value for the radiant flux ?soll for the duration of the recording mode. According to the invention, the illuminance is increased to a radiant flux above the specified value ?soll for the recording mode and lowered to a radiant flux below the specified value for the radiant flux ?soll for a specified period of time after the recording mode has finished. Although the proposed method for adapting the illuminance is provided for slit lamp microscopes, it can be used for any ophthalmological device that has both an observation mode and a recording mode to obtain high-quality, well-lit recordings in the recording mode.

Abstract: Methods and systems am disclosed in which an optical diagnosis of an eye's optical image quality is performed using a simulated retinal image. An objective measurement of a total wave aberration is obtained, and residual aberrations are computed by subtracting a sphero-cylindrical correction from the total wave aberration. The simulated retinal image is computed by computing a point-spread function from the residual aberrations and convolving the computed point-spread function with an acuity chart. The optical diagnosis includes at least one of: determining excess aberrations, ranking optics of the eye into optical grades, selecting the eye for high-definition eyeglasses, identifying amblyopia or macular diseases, or choosing an objective refraction for vision correction.

Abstract: An instrument includes: one or more scanning mirrors to receive an OCT sample beam and to scan the sample beam in two orthogonal directions; and an optical system to receive the sample beam and provide the sample beam to an eye. The optical system includes: a first lens having a first focal length, disposed along an optical path from the scanning mirror(s) to the eye at a distance from the cornea which is approximately equal to the first focal length, and a second lens disposed along the optical path between the first lens and the scanning mirror(s). The second lens receives the sample beam from the scanning mirror(s) and provides the sample beam to the first lens as a converging beam such that, as the sample beam is scanned, the sample beam passes through a pivot point located along an optical axis between the eye and the first lens.

Abstract: An ophthalmic apparatus includes an acquiring unit, an OCT unit, an analyzer, and a calculator. The acquiring unit is configured to acquire a dioptric power in a first region including a fovea of a subject's eye. The OCT unit is configured to acquire OCT data of a fundus of the subject's eye using optical coherence tomography. The analyzer is configured to specify a shape of the fundus by analyzing the OCT data. The calculator is configured to calculate a dioptric power in a peripheral region of the first region of the fundus based on the dioptric power in the first region and the shape of the fundus.

Abstract: In an embodiment, multiple conjugate planes are used to create a plurality of optical pupil planes and a plurality of image planes. These optical planes solve multiple problems and introduce significant performance enhancements in the system. In one implementation of a disclosed embodiment, the measurement channel is based on the reverse Shack-Hartmann principle. By introducing a relay system (for example a 4-f lens system) the slit plane could be made conjugate to the measured system pupil plane (unlike a previous implementation where the slits were places away from the pupil plane as it was not accessible directly). Creating a virtual pupil plane allows for more accurate placement of the plane without the need for contact with the measured optical system.

Abstract: Embodiments relate to an optical trial frame that includes: left and right frames extending in the left and right directions respectively; a bridge located between and connected to the left and right frames such that the left and right frames can move relative to each other along a longitudinal axis of the bridge; left and right temples connected to the respective left and right frames; left and right lens holders rotatably coupled to the left and right frames respectively and configured to receive and retain lenses in use; and, capacitive sensing means configured to detect and measure at least one of: a lateral position of one of the frames; and, a rotational position of one of the lens holders.

Abstract: The technology described herein is directed to a fundus camera and, more specifically, to a fundus camera having a display that projects active visual alignment stimuli onto an eye of an examinee via one or more components of an optimal assembly. The active visual alignment stimuli are dynamically adjusted to guide an examinee toward optical alignment for fundus imaging.

Abstract: According to an aspect of an embodiment, a method for detection of at least one single nucleotide polymorphism (SNP) in a human subject from assaying a combination of SNPs can include: a) obtaining a nucleic acid sample from said human subject; b) genotyping the sample for a combination of Alzheimer's disease associated genes(s) RTTN, ALCAM/CD166, DMXL2, and DYNLL1, said combination of SNP alleles being the following: rs4891826 (G), rs2030515 (G), rs7164265 (C), and rs993900 (A); and c) detecting in said nucleic acid sample the presence of at least one of: a G for rs4891826, a G for rs2030515, a C for rs7164265, or an A for rs993900.

Abstract: Provided herein are medical devices comprising a plurality of biologically interactive devices configured for interacting with a large area biological surface. The biologically interactive devices each may comprise a sensor for measuring a physiological parameter. A wireless controller is configured to wirelessly operate the plurality of biologically interactive devices. A wireless transmitter is configured for wirelessly communicating an output from said plurality of biologically interactive devices to a remote receiver. The medical devices are particularly suited for measuring one or both of pressure and temperature, with compatibility for incorporating additional sensors of interest.

Abstract: A user-wearable fluorescence based visualization system comprising a multi-light lamp assembly that provides for the selected output of light using multiple light emitting sources, wherein the outputted light may be tailored to generate response wavelength by the interaction of the emitted light and a tissue illuminated by the emitted light, through the process of fluorescence, and a viewing system that allows a practitioner view the fluorescent light generated by the tissue, and distinguish between healthy and diseased tissues.

Abstract: In some examples, an apparatus may include a laser, a source fiber that delivers the laser radiation to an object, and a detector fiber that receives scattered laser radiation and illuminates a detector array with the scattered laser radiation to form speckles on the detector array. In some examples, the object may be directed illuminated by a laser. The detector array may include a plurality of detectors, and may be positioned to receive the scattered laser radiation from the end of the detector fiber. The distance between the detector array and the end of the detector fiber may be adjustable. A controller may be configured to receive detector data from the detector array, determine a time-dependent intensity autocorrelation function for each detector of a plurality of detectors, and determine an ensemble average autocorrelation function. The apparatus may provide information relating to dynamic processes within the object. Various other methods, systems, and computer-readable media are also disclosed.

Abstract: Disclosed is a visual imaging device based on PS-OCT for early demineralization and caries of dental hard tissues, comprising a laser light source for emitting a laser light, a coupler for receiving and dividing the laser light emitted by the laser light source into a reference laser light and a detection laser light; wherein the reference laser light backtracking to the coupler and the detection laser light backtracking to the coupler are coupled and then passed through a transmission grating and a convex lens to input as an optical signal into a linear CCD detector for converting the optical signal into an electrical signal which is then input to a computer control system and collected by a built-in capture card; and the computer is configured to perform a three-dimensional reconstruction of an image and perform two-dimensional cross-section image analysis; and the computer control system is connected to the scanning galvanometer to control a vibration of the scanning galvanometer.

Abstract: There is provided an apparatus (12) for use with a wearable cuff (14) in measuring blood pressure. The cuff (14) is inflatable to pressurize a measurement site (20) of a subject (18). The apparatus (12) is configured to estimate a size of the cuff (14) during a current inflation of the cuff (14) and compare the estimated size of the cuff (14) to a previous size of the cuff (14) estimated during an inflation of the cuff (14) that immediately preceded the current inflation of the cuff (14). The apparatus (12) is also configured to, if the estimated size of the cuff (14) differs from the previous size of the cuff (14) by more than a predefined amount, change a pressure up to which the cuff (14) is inflated before deflation of the cuff (14) starts.

Abstract: An apparatus, system, and method are disclosed for monitoring the motion, breathing, heart rate of humans in a convenient and low-cost fashion, and for deriving and displaying useful measurements of cardiorespiratory performance from the measured signals. The motion, breathing, and heart rate signals are obtained through a processing applied to a raw signal obtained in a non-contact fashion, typically using a radio-frequency sensor. Processing into separate cardiac and respiratory components is described. The heart rate can be determined by using either spectral or time-domain processing. The respiratory rate can be calculated using spectral analysis. The sensor, processing, and display can be incorporated in a single device which can be worn or held close to the body while exercising, or alternately placed in a fixed piece of exercise equipment at some distance form the body, and may also be integrated with other sensors, such as position locators.

Abstract: The reliability of calculated bio-information of a subject is determined. When the reliability of the bio-information is determined to be high, the bio-information is output, whereas when the reliability of the bio-information is determined to be low, the bio-information is not output. Thus, among the calculated bio-information, only the bio-information of high reliability may be output, or distinctive display may be performed depending on the reliability, whereby it is possible to provide a bio-information output device and the like capable of easily determining bio-information of high reliability.

Abstract: Computer-implemented methods and systems are provided for quantitative hemodynamic flow analysis, which involves retrieving patient specific image data. A 3D reconstruction of a vessel of interest can be created from the patient specific image data. Geometric information can be extracted from the 3D reconstruction. A lesion position can be determined. Patient specific data can be obtained. Hemodynamic results can be calculated based on the geometric information, the lesion position and the patient specific data.

Abstract: A biological information analysis apparatus includes a sensor data acquirer that acquires biological information of a user measured by a sensor, a data analyzer that analyzes time-series data for the biological information over a plurality of time intervals and, from multiple pieces of biological information that were acquired at mutually corresponding times of measurement in respective ones of the plurality of time intervals, calculates representative values for the multiple pieces of biological information, a measurement anomaly detector that detects an anomaly contained in the measured biological information based on time-series data with the representative values calculated by the data analyzer or on the time-series data for the multiple pieces of biological information that was used in calculation of the time-series data with the representative values, and a presenter that outputs the calculated representative values for the multiple pieces of biological information and information indicating the detecte

Abstract: An optical channel, of an optical filter, passes light associated with a particular wavelength range to a sensor element, of an optical sensor, that operates in a gated mode. One or more processors obtain, from the optical sensor, a first optical measurement and a second optical measurement related to a multi-layered subject. The first optical measurement indicates an amount of light associated with the particular wavelength range that the sensor element accumulated during a first time range, and the second optical measurement indicates an amount of light associated with the particular wavelength range that the sensor element accumulated during a second time range. The first time range is a subrange of the second time range. The one or more processors process the first optical measurement and the second optical measurement to determine one or more parameters associated with the multi-layered subject.

Abstract: Approaches for evaluating fluid flow based on fluorescent sensing is disclosed. In one approach, a nanoparticle injector is configured to inject nanoparticles into fluid flowing through a conduit. A detector is configured to determine a presence of the nanoparticles in the flow of the fluid. The detector can include a radiation source configured to irradiate the fluid with a target radiation and a fluorescent meter configured to measure an amount of fluorescence emitted from the fluid irradiated with the radiation. A control unit is configured to determine the flow of the fluid in the conduit as a function of the measured amount of fluorescence.

Abstract: A portable device for quantitative measurement of tissue autoregulation and neurovascular coupling via portable measurement of blood flow, oxygenation, metabolism, and/or EEG signals and methods for using said device. The device may comprise a body and a plurality of legs pivotably attached to the body. The plurality of legs may comprise at least one reference electrode leg and at least one measurement electrode leg for electrical measurement, and an optical detection fiber leg and at least one optical source fiber leg for optical blood flow, oxygenation, and metabolism measurement. The present invention is additionally directed to a portable device for blood flow measurement and therapeutic photobiomodulation. The device may comprise a body and a plurality of legs. The plurality of legs may comprise at least one optical detection fiber leg and at least one optical source fiber leg, and at least one leg for therapeutic photobiomodulation.

Abstract: Non-invasive measurement of intracranial pressure (ICP), for example mean ICP. A probe adjacent the head emits energy, such as ultrasound, and receives reflected signals. A processing unit derives ICP waveform from the signals. A pressure mechanism applies external pressure intermittently to outer surface of the head and incrementally increases the external pressure. The processing unit is configured to detect a decrease in amplitude of the ICP waveform (occurring in some embodiments only after an intermediate period of ICRS compensation), the processing unit configured to determine the ICP of the person from a sum of applied external pressures from a time of the initial value A1 until a final value at which the amplitude remains stable with additional increase in applied external pressure. In some cases, the final value is earlier than that but the processing unit extrapolates the sum to when the amplitude remains stable with additional increases in pressure.

Abstract: An electrocardiogram detection device is provided. The electrocardiogram detection device includes a filter amplifier and a microcontroller. The filter amplifier filters and amplifies a raw heartbeat signal of a user. The microcontroller is coupled to the filter amplifier. The microcontroller generates a control signal according to a trigger signal to control the filter amplifier to filter out components of the raw heartbeat signal in a specific bandwidth range.

Abstract: A bio-processor, a bio-signal detecting system, and an operation method of the bio-processor are provided. The bio-processor includes a bioelectrical impedance sensor and a digital signal processor. The bioelectrical impedance sensor measures bioelectrical impedance during a sensing time including a portion of a settling time. The digital signal processor estimates a settled bioelectrical impedance value based on changes in the measured bioelectrical impedance. The digital signal processor generates bio-data based on the settled bioelectrical impedance value. The bio-processor reduces a time when a bio-signal is measured and ensures accuracy of the settled bioelectrical impedance value.

Abstract: A measuring instrument is provided for inserting into an oral cavity with a narrow opening and that enables intraoral measurement in such a way as to relieve stress exerted on a probe part of the measuring instrument. The measuring device is configured to ensure that the probe part is accurately pressed against the oral mucosa of a person subjected to measurement. The measuring instrument includes a grip and a probe. The probe includes a measurement section and a joint forming a connection between the measurement section and grip. The measurement section is a tip region of the probe and provided with the sensor having an exposed measurement surface. A circuit board is disposed in the joint. The circuit board is an oscillation circuit board on which members forming an oscillation circuit are mounted. The oscillation circuit outputs an oscillatory signal corresponding to an electrical signal transmitted from the sensor.

Abstract: Apparatus and methods are described including a processor (20) configured to receive first and second sets of extraluminal images of a lumen, the second set being acquired while an endoluminal device is being moved through the lumen. The processor designates at least one of the first set of images as a roadmap image, and designates, within the lumen in the roadmap image, a roadmap pathway (42). A plurality of features (44, 46, 48, 50) that are visible within at least some of the second set of extraluminal images are identified, and an arrangement of three or more of the features within the image are compared to a shape of at least a portion of the roadmap pathway. Based upon the comparing, the identified features are mapped to locations along the roadmap pathway within the roadmap image. Other applications are also described.

Abstract: A medical tracking system including a medical trackable structure configured to be inserted in a body of a patient, a control circuit, and a sensor is provided. The medical trackable structure includes a permanent magnet, and a coil arranged adjacent to the permanent magnet. The control circuit is configured to apply an excitation signal to the coil and rotate the permanent magnet. The permanent magnet is configured to generate a magnetic field including harmonics during the rotation, based in part on the excitation signal applied to the coil. The sensor is configured to sense the harmonics included in the magnetic field and to output to the control circuit a sensor signal based on the magnetic field. The control circuit further calculates position information associated with the medical trackable structure within the body of the patient based on the sensor signal.

Abstract: The invention discloses a gastrointestinal motility measurement system based on a digestive tract capsule, which comprises a data acquisition module, a data processing module and a capsule. The data acquisition module is configured in the capsule, and comprises an ultrasonic distance measuring device or a 3D camera for acquiring a depth map or a point cloud of the inner wall of the digestive tract; The data processing module is used for processing the depth map or the point cloud to obtain the surface data of the inner wall surface of the digestive tract; Further extraction of morphological features, including the inner wall of the digestive tract, curvature, inner diameter and volume, can be used as a reference for the evaluation of gastrointestinal motility.

Abstract: A method comprising at least one light source configured to generate a light of at least one wavelength and project the light over an optical path, a sample device, the device containing a sample obtained from exhalation of a person, a vortex mask configured to receive the light after the light passes through at least a portion of the sample device, the vortex mask including a series of concentric circles etched in a substrate, the vortex mask configured to provide destructive interference of coherent light received from the at least one light source, a detector configured to detect and measure wavelength intensities from the light in the optical path, the wavelength intensities being impacted by the light passing through the sample, the detector receiving the light that remained after passing through the vortex mask, and a processor configured to provide measurement results based on the wavelength intensities.

Abstract: A method comprising at least one light source configured to generate a light of at least one wavelength and project the light over an optical path, a sample device, the device containing a sample obtained from exhalation of a person, a vortex mask configured to receive the light after the light passes through at least a portion of the sample device, the vortex mask including a series of concentric circles etched in a substrate, the vortex mask configured to provide destructive interference of coherent light received from the at least one light source, a detector configured to detect and measure wavelength intensities from the light in the optical path, the wavelength intensities being impacted by the light passing through the sample, the detector receiving the light that remained after passing through the vortex mask, and a processor configured to provide measurement results based on the wavelength intensities.

Abstract: A method comprising at least one light source configured to generate a light of at least one wavelength and project the light over an optical path, a sample device, the device containing a sample obtained from exhalation of a person, a vortex mask configured to receive the light after the light passes through at least a portion of the sample device, the vortex mask including a series of concentric circles etched in a substrate, the vortex mask configured to provide destructive interference of coherent light received from the at least one light source, a detector configured to detect and measure wavelength intensities from the light in the optical path, the wavelength intensities being impacted by the light passing through the sample, the detector receiving the light that remained after passing through the vortex mask, and a processor configured to provide measurement results based on the wavelength intensities.

Abstract: An artificial intelligence-based system and method for scalable screening of individuals for respiratory infection, such as COVID-19. The system is trained to distinguish distinct latent features of cough sounds produced by a COVID-19 infected person from cough sounds produced by patients suffering from any other respiratory infection or involuntary cough sounds produced by a healthy person. Cough sound samples from individuals can be remotely collected and evaluated by the system for likelihood of the COVID-19 infection. Additionally, images of affected body parts, biomarkers, metadata, and other respiratory sound samples can also be used for screening.

Abstract: The present invention relates to quality control of pulmonary function test (PFT) devices. In particular, but not by way of limitation, the present invention relates to systems and methods for characterizing or verifying the measurement accuracy of pulmonary function testing devices used for measuring dynamic lung volumes (tidal volume (TV), inspiratory reserve volume (IRV), expiratory reserve volume (ERV), divisions thereof, and any other suitable dynamic lung volume) using spirometry, static and/or absolute lung volumes (total lung capacity (TLC), residual volume (RV), divisions thereof, and any other suitable absolute lung volume) using washout, dilution, and/or plethysmographic methods, and/or gas exchange, such as single-breath determination of carbon monoxide uptake in the lung (DLCO).

Abstract: A sensor-based quantification and analysis system includes an input device including a plurality of sensors that generate an input based on a force. The input device also includes a transmission device that transmits force information based on the input. The system also includes an output device that receives the force information. A processing unit selects, for each of the plurality of sensors, one of a plurality of levels of a likelihood of tissue damage based on the force and a predetermined time period. Further, the output device includes a display that presents or logs the one of the plurality of levels of the likelihood of tissue damage for each of the plurality of sensors.

Abstract: A caliper type device is provided for identifying the cranial midline on a patient. The device includes a pair of arms have first ends for receipt in a patients ears, and opposite, pivotally connected second ends which allow the arms to open and close to fit to different sized heads of various patients. A housing at the second end of the arms holds a laser pointer or other tool for identifying the cranial midline after the device is positioned on the patients head.

Abstract: Accuracy enhancing systems, devices and methods are provided using data obtained from inertial measurement units (IMUs). IMUs are provided on one or more of a patient, surgical table, surgical instruments, imaging devices, navigation systems, and the like. Data from sensors in each IMU is collected and used to calculate absolute and relative positions of the patient, surgical table, surgical instruments, imaging devices, and navigation systems on which the IMUs are provided. The data generated by the IMUs can be coupled with medical images and camera vision, among other information, to generate and/or provide surgical navigation, alignment of imaging systems, pre-operative diagnoses and plans, intra-operative tool guidance and error correction, and post-operative assessments.

Abstract: An apparatus for producing information indicative of cardiac abnormality, for example Heart failure with preserved ejection fraction “HFpEF”, includes a signal interface for receiving a signal indicative of cardiac motion and a processing system coupled to the signal interface. The processing system is configured to extract, from the signal, temporal portions which belong to diastolic phases of a heart. The processing system is configured to set an output signal of the apparatus to express presence of cardiac abnormality based on a result of a comparison between the indicator quantity and a threshold value.

Abstract: A skeleton extraction unit (120) extracts skeleton information expressing in a time series a motion of a skeleton of a person from two-dimensional video data (161) obtained by capturing a walking movement of the person. A walk analysis unit (130) calculates walk analysis data (31) including arm swing information expressing an arm swing state of the person in walking and gait information expressing a gait state of the person in walking, using the video data (161). A determination unit (150) compares a determination threshold value (164) for determining a fatigue degree of the person with the walk analysis data (31) of the person, and determines the fatigue degree of the person using a comparison result. The determination threshold value (164) includes a threshold value of the arm swing information and a threshold value of the gait information.

Abstract: A system and method for human motion detection and tracking are disclosed. In one embodiment, a smart device having an optical sensing instrument monitors a stage. Memory is accessible to a processor and communicatively coupled to the optical sensing instrument. The system captures an image frame from the optical sensing instrument. The image frame is then converted into a designated image frame format, which is provided to a pose estimator. A two-dimensional dataset is received from the pose estimator. The system then converts, using inverse kinematics, the two-dimensional dataset into a three-dimensional dataset, which includes time-independent static joint positions, and then calculates, using the three-dimensional dataset, the position of each of the respective plurality of body parts in the image frame.

Abstract: A human body detection device including line-shaped piezoelectric substrates respectively provided in each of a plurality of regions in a plate material intersecting a direction of pressure received from a human body, and provided such that an axial direction of each of the piezoelectric substrates runs along the plate material so as to detect pressure applied in a radial direction of the piezoelectric substrate, memory, and a processor coupled to the memory. The processor is configured to be capable of detecting an output signal from each of the piezoelectric substrates.

Abstract: A mouth guard, or wearable device, senses impact forces, calculates risk factors for injury, and displays status of risk and potential injury. A mouth guard may be used to identify, treat and prevent exacerbating brain injury. A wearable device can be programmed with biometric data to better calculate and anticipate impact thresholds and more precisely predict and prevent injury.

Abstract: Devices for determining the likelihood that a user of a primary monitoring device (“PMD”) has developed a medical condition, generally comprising sensors coupled to the PMD, wherein the PMD detects changes to sensor readings over time, and wherein the changes indicate a change in the likelihood that a user of the PMD has developed a medical condition. In some embodiments, motion sensors are operably coupled to the PMD, and the PMD monitors and saves data relating to characteristics of motion detected, which are used to determine whether there has been a change in a likelihood that a user is undergoing a medical event. In further embodiments, the PMD comprises cameras, and the PMD monitors and saves data relating to movement of a user's eyes, which is utilized to determine whether there has been a change to a likelihood that the user is currently undergoing a medical event.