Methods for calculating a MetaKG signal are provided. The method including illuminating a region of interest in a sample with a near-infrared (NIR) light source and/or a visible light source. The region of interest includes a sample portion and background portion, each having a different set of optical characteristics. Images of the region of interest are acquired and processed to obtain metadata associated with the acquired images. MetaKG signals are calculated for the region of interest and for the background. The MetaKG signal for the background is used to adjust the MetaKG signal for the region of interest to provide a final adjusted MetaKG signal for the region of interest.

A monitoring system a user activity sensor to determine patterns of activity based upon the user activity occurring over time.

A probe device includes an optical device including at least one of a photodetector or a first light source. A cover structure is included and is arranged in front of the optical device. The cover structure includes an electrode which contacts, in use, a body tissue.

Hearing aid system comprising at least one hearing aid is provided. The hearing aid system further comprising an input unit for receiving an input sound signal from an environment of the hearing aid user and providing at least one electric input signal representing said input sound signal, an output unit for providing at least one set of stimuli perceivable as sound to the hearing aid user based on processed versions of said at least one electric input signal, a processing unit connected to said input unit and to said output unit and comprising signal processing parameters to provide said processed versions of said at least one electric input signal, at least one photoplethysmogram (PPG) sensor configured to provide a PPG signal of the hearing aid user, and a listening effort determination unit configured to provide at least one PPG morphology parameter value based at least on the PPG signal, compare the at least one PPG morphology parameter value with at least one corresponding reference PPG morphology parameter value and determine a morphology comparison measure, and determine a listening effort of the hearing aid user. A hearing aid is further provided.

A consumer product that is a portable and, in some cases, a wearable electronic device. The wearable electronic device may have functionalities including: keeping time; monitoring a user's physiological signals and providing health-related information based on those signals; communicating with other electronic devices or services; visually depicting data on a display; gather data form one or more sensors that may be used to initiate, control, or modify operations of the device; determine a location of a touch on a surface of the device and/or an amount of force exerted on the device, and use either or both as input.

A system for monitoring medical conditions including pressure ulcers, pressure-induced ischemia and related medical conditions comprises at least one sensor adapted to detect one or more patient characteristic including at least position, orientation, temperature, acceleration, moisture, resistance, stress, heart rate, respiration rate, and blood oxygenation, a host for processing the data received from the sensors together with historical patient data to develop an assessment of patient condition and suggested course of treatment, including either suspending or adjusting turn schedule based on various types of patient movement. Compliance with Head-of-Bed protocols can also be performed based on actual patient position instead of being inferred from bed elevation angle. The sensor can include bi-axial or tri-axial accelerometers, as well as resistive, inductive, capacitive, magnetic and other sensing devices, depending on whether the sensor is located on the patient or the support surface, and for what purpose.

A method and apparatus for testing relating to the technical field of test. The method includes: in response to a situation that the two hands of a to-be-tested user are placed in a preset interaction area of the test apparatus, performing the following test steps: transmitting an electric signal to the two hands, and receiving a feedback signal of the two hands, wherein the feedback signal is used for generating electrical impedance information of the two hands; testing a bioelectric signal of the two hands, wherein the bioelectric signal is used for generating electrocardio information of said user; emitting light having a preset wavelength to the two hands, and receiving reflected light by using a photosensitive sensor in the test apparatus, wherein the reflected light is used for generating blood flow-related index information of said user.

A spectrally encoded flow cytometry (SEFC) technique for imaging blood in the microcirculation. Since the dependency of one of the axes of the image on time prevents effective quantification of essential clinical parameters, the optical path in an SEFC system is split into two parallel imaging lines, followed by data analysis for recovering the flow speed from the multiplexed data. The data analysis may be auto-correlation of a pair of images obtained from a sequence of images of the imaged blood vessel.

Disclosed is an optical coherence tomography (OCT) system according to an exemplary embodiment of the present disclosure. The OCT system may include: a light source unit generating light; an optical interferometer including an optical coupler splitting the light generated by the light source unit into first distribution light and second distribution light, a reference arm reflecting the first distribution light, a sample arm reflecting the second distribution light, and an optical detector detecting the light reflected by the reference arm and the sample arm; an OCT catheter including an optical fiber having a shape in which the optical fiber is insertable into at least a part of a human body and is rotatable and discharging the light to a tissue and collecting OCT data for the tissue; an OCT engine including a processor and a storage unit and processing the OCT data collected by the OCT catheter; and an OCT controller connected to a proximal end of the OCT catheter and controlling rotation of the OCT catheter.

A biological information detection device includes: a video capture unit, a blood flow analysis unit, a local pulse wave detection unit, a pulse wave propagation velocity calculation unit, and a blood pressure estimation unit. The video capture unit obtains video information on a face of a living body. The blood flow analysis unit analyzes video data of at least three skin areas in the video information, as blood flow information. The local pulse wave detection unit is provided for each skin area to calculate pulse information based on the blood flow information sequenced chronologically. The pulse wave propagation velocity calculation unit calculates a pulse wave propagation velocity based on a phase difference between pieces of the pulse information at each skin area calculated by the local pulse wave detection unit. The blood pressure estimation unit estimates blood pressure based on the pulse wave propagation velocity.