An electrochemical sensor for humoral detection and a detection device. The electrochemical sensor for humoral detection includes a material layer including at least one hydrophilic region; and at least one detection unit, located in the hydrophilic region. The hydrophilic region includes a sampling port configured to be in contact with a liquid sample (for example, saliva) to be detected, the detection unit includes a working electrode and an opposed electrode disposed apart from each other, the working electrode comprises a reaction surface containing a substance configured to have a reaction with an analyte in the liquid sample, and the working electrode and the opposed electrode are configured to detect an electrical signal generated by the reaction so as to detect the analyte.

A health monitoring device is provided, and may be used in population health monitoring and disease tracing, as well as for individual subject health purposes. The health monitoring device comprises a triboelectric nanogenerator (TENG) for generating and storing electrical energy from mechanical activity of a user. The device provides a continuous and uninterrupted stream of physiological data received at a surface of the device in contact with a surface of the user. The triboelectric nanogenerator is a paper-based device comprising a paper-based material layer and a polydimethylsiloxane/polytetrafluoroethylene (PDMS/PTFE) material layer, each on a copper film. The device has enhanced sensitivity to motion, providing an improved device capable of converting small amounts of movement into electrical energy, and of recording and transmitting data of small physiological changes of a user to a receiver. The device is lithium free, and eliminates the necessity of recharging.

A method of monitoring eye strain includes detecting the blink status, the vergence status and the pupil status of a user, and then determining whether the user encounters eye strain according to at least one of the blink status, the vergence status and the pupil status of the user. The method further includes facilitating the user to blink or informing the user of eye strain.

A computer-implemented method for indicating a long-term stress level of a person by means of a data processing unit, including the steps of acquiring stressor data having a set of stressor data items; analyzing stressor data values of the stressor data items by means of an artificial neural network to generate data representing a stress level, wherein the artificial neural network (ANN) is trained to provide output representing the stress level based on the stressor data values and an indication of previous stress state; and signaling the stress level.

An intelligent defecation device for living creature includes a device body, a supporting portion, an image module, and a first analysis module. The supporting portion is formed within the inner side of the device body for accommodating a moisture absorption member so as to allow the living creature to leave over its excrement therein. The image module is also arranged at the device body for dynamically capturing the images of the excrement in the supporting portion and outputting the image. The first analysis module is arranged in the device body and connected with the image module to analyze and calculate the defecation mode with the image based on preset or accumulated data, so as to generate a signal when an abnormal defecation mode is diagnosed.

A wireless patient monitoring system includes a host device configured to pair with one or more wireless physiological sensors to receive physiological data therefrom. The host device includes a nearfield communication (NFC) transmitter emitting an electromagnetic field. The system includes at least one wireless physiological sensor having a sensing element that senses physiological parameter information from a patient, a battery, and a field detection circuit configured to detect NFC field and to generate an activation signal thereupon. A sensor controller is configured to operate in a sleep state that maximizes battery power consumption by the wireless physiological sensor and to receive the activation signal from the field detection circuit when the NFC field is detected. After receipt of the activation signal, the sensor controller operates the wireless physiological sensor in an activated mode that enables full power consumption by the wireless physiological sensor.

On-body analyte sensors may be designed for extended wear to provide ongoing measurement of physiological analyte levels. However, on-body analyte sensors may be susceptible to damage or dislodgment during wear due to routine interactions that occur with one's surroundings. Guard rings may be adapted to protect on-body analyte sensors from such interactions. Guard rings may comprise an annular body comprising an inner perimeter face, an outer perimeter face, a top edge, and a bottom face adapted for contacting a tissue surface. The inner perimeter face is shaped to circumferentially surround a sensor housing of an on-body analyte sensor. At least a portion of the outer perimeter face defines a chamfered surface extending between the top face and the bottom face. Adhesive pads or strips may further be engaged with the guard rings and aid in securing the guard rings to a surface, such as skin.

A method for optimizing sleep for a user of a respiratory therapy system is described herein. The method includes receiving therapy instructions to be implemented using the respiratory therapy system for a sleep session. The therapy instructions include a plurality of prescribed control parameters, each of the plurality of prescribed control parameters having a value or a range of values. The method further includes receiving a desired sleep comfort level for the sleep session, and adjusting one or more of the values or the range of values of the plurality of prescribed control parameters, to one or more adjusted values or range of values based on the desired sleep comfort level. The adjustments to the adjusted values are implemented to aid the user in achieving the desired sleep comfort level.

A method may include generating a frequency-agnostic signal using an adjustable oscillator, and applying the frequency-agnostic signal to a user. The method may also include determining a reflecting value based on the frequency-agnostic signal as reflected by the user. The method may additionally include identifying a peak in the reflecting value by at least repeatedly comparing the determined reflecting value to a previously stored highest reflecting value, and adjusting the adjustable oscillator based on the comparison. The method may also include, after identifying the peak, determining a frequency of the oscillator corresponding to the peak, and outputting the frequency of the oscillator.

The invention provides a system (1) comprising a sensor (100) for measuring a skin parameter, the sensor (100) comprising (i) a plurality of spatially separated light sources (110) configured to provide light source light (111), and (ii) a detector (120) configured at a first distance (d1) from each of the light sources (110), wherein the first distance (d1) is selected from the range of 5-80 mm, wherein the sensor (100) is configured to provide the light source light (111) with optical axes (OL) under an angle (α) relative to an optical axis (O2) of the detector (120) selected from the range of 10-80°, wherein the sensor (100) comprises at least three light sources (110), wherein the light sources (110) are configured to provide unpolarized light source light (111), wherein the sensor (100) further comprises (iii) a sensor opening (107) downstream of the light sources (110) and upstream of the detector (120) for propagation of the light source light (111) out of the sensor (100) and for entrance of reflected sensor light (111) into the sensor (100), and (iv) a sensor window (150), of a material (151) transmissive for the light source light (111), configured downstream of the light sources (110), configured upstream of the sensor opening (107), and configured upstream of the detector (120) with a second distance (d2) to the sensor opening (107) of at least 3 mm.