Abstract: In some embodiments, an insertion device for a robotic surgery apparatus can include a first portion with a plurality of instrument channels configured to removably house a plurality of surgical instruments and first and second camera channels positioned in an interior of the first portion and extending along substantially the entire length of the first portion. The first camera channel can removably house a primary camera tube, and the second camera channel can include a secondary camera. The device can include a second portion with an insertion channel terminating at a first end with a first opening permitting the primary camera tube to pass through and terminating at a second end opposite the first end with a second opening aligned with the first camera channel of the first portion. The insertion channel can permit the primary camera tube to pass through the insertion channel and enter the first camera channel.

Abstract: A method and apparatus for processing gastrointestinal (GI) images are disclosed. According to this method, a regular image is received, where the regular image is captured using an imaging apparatus by projecting non-structured light onto a body lumen when the imaging apparatus is in the body lumen. One or more structured-light images captured using the imaging apparatus by projecting the body lumen with structured light are received. A target distance for a target region in the regular image is derived based on said one or more structured-light images. A filter is determined based on the target distance and camera parameters associated with the imaging apparatus. A first processed target region is generated by applying the filter to the target region to improve sharpness of the target region. A first processed regular image comprising the first processed target region is provided.

Abstract: A light source device includes a primary light source that emits primary light, a light guide that guides the primary light, an optical conversion unit that converts the primary light emitted from the light guide and having a first light distribution angle into secondary light having a second light distribution angle and emits the secondary light, and a light distribution adjustment unit that adjusts the secondary light to illumination light having a third light distribution angle and emits the illumination light. The light distribution adjustment unit and the optical conversion unit slide each other. The light distribution adjustment unit allows a light distribution adjustment amount for adjusting the second light distribution angle of the secondary light to adjust to the third light distribution angle of the illumination light.

Abstract: An endoscope apparatus includes: a light-emitting element; a rolling shutter-type image pickup device allowing an exposure period in which the plurality of lines are simultaneously exposed and a reading period in which image pickup signals of the respective lines are sequentially read to be alternately switched to each other; and a control section. The control section controls an intensity of the light emitted by the light-emitting element. The control section can perform switching between a first illumination mode in which the light is applied from the light-emitting element in the exposure period and the reading period and a second illumination mode in which the light is applied from the light-emitting element only in the exposure period, and if the intensity of the light is controlled so as to have a predetermined value, performs control to switch one of the first mode and the second mode to the other.

Abstract: A virtual reality-based ophthalmic inspection system includes a wearable unit, an electronic unit, and at least one detector; the wearable unit is available for an inspected object to wear the wearable unit on head; the electronic unit is assembled with the wearable unit and has a left-eye display zone and a right-eye display zone, wherein the left-eye display zone is used for displaying at least one left-eye sight-targets, and the right-eye display zone is used for displaying at least one right-eye sight-targets; the detector is disposed on the electronic unit. A sight-target with at least one distinguishing feature are shown on one of the left-eye display zone and the right-eye display zone, the left-eye display zone displays the sight-target while the right-eye display zone is filled with black, and the right-eye display zone displays the sight-target while the left-eye display zone is filled with black.

Abstract: Provided is a snapshot spectral domain optical coherence tomographer comprising a light source providing a plurality of beamlets; a beam splitter, splitting the plurality of beamlets into a reference arm and a sample arm; a first optical system that projects the sample arm onto multiple locations of a sample; a second optical system for collection of a plurality of reflected sample beamlets; a third optical system projecting the reference arm to a reflecting surface and receiving a plurality of reflected reference beamlets; a parallel interferometer that provides a plurality of interferograms from each of the plurality of sample beamlets with each of the plurality of reference beamlets; an optical image mapper configured to spatially separate the plurality of interferograms; a spectrometer configured to disperse each of the interferograms into its respective spectral components and project each interferogram in parallel; and a photodetector providing photon quantification.

Abstract: An eyelid detection device includes a face feature point detecting unit for detecting outer and inner eye corners as face feature points from a captured image, an eye region detecting unit for detecting an eye region including both an upper eyelid area and an eye area from the captured image on the basis of the face feature points, and an upper eyelid detecting unit for, for each of a plurality of divided areas into which the eye region is divided, detecting the boundary between the upper eyelid area and the eye area on the basis of the pattern of arrangement of the intensity values of pixels aligned in the divided region, and for connecting the boundary detected for each of the divided regions, to determine an upper eyelid.

Abstract: The present invention relates generally to systems and methods for measuring an analyte in a host. More particularly, the present invention relates to systems and methods for transcutaneous measurement of glucose in a host.

Abstract: An operating microscope including an optical unit for forming an image of an object plane in oculars of the microscope, an optoelectronic image receiver coupled to the microscope and optics to form images, of objects placed in a region between a front objective of the microscope and an object plane of the microscope, on the optoelectronic image receiver. The microscope has a magnification factor of the optics to form images, and a system to detect optical markings forming a markings pattern placed on a surgical instrument or an object placed in the region between the front objective of the microscope and the object plane of the microscope. The system calculates a geometrical position and orientation of the markings pattern in relation to the optoelectronic image receiver, relative to the microscope.

Abstract: An optical measuring device including a light source, a light beam path adjuster, a light detector and a controller is provided. The light source may emit light toward an object in a predetermined progress direction. The light beam path adjuster may be disposed between the light source and the object and may change a progress path of the light emitted from the light source. The light detector may receive the light that is reflected from the object after passing through the light beam path adjuster. The controller may compare a first effective beam path length of the reflected light that the light detector receives with a predetermined target beam path length and control a refractive angle of the light beam path adjuster based on a beam path length difference between the first effective beam path length and the predetermined target beam path length.

Abstract: Some embodiments relate to a device, method, and/or computer-readable medium storing processor-executable process steps to remove a component of a signal corresponding to ambient light in a photoplethysmographic sensor device, including capturing a first detected light signal representing an ambient light at a first time, causing a light emitter to generate a source light signal driven at a first level, capturing a second detected light signal representing the source light signal after interacting with a user's tissue plus the first detected light signal, generating a first output signal based on the second detected light signal adjusted by the first detected light signal, causing the light emitter to generate a source light signal driven at a second level, capturing a third detected light signal representing the source light signal driven at the second level after interacting with the user's skin plus the first detected light signal, and generating a second output signal based on the third detected light sig

Abstract: A photo-acoustic sensing apparatus (100) for non-invasive measurement of blood parameters of a subject (102) comprises a photo-acoustic sensor (104) for sensing photo-acoustic signals (106) induced when a region of the subject is illuminated by a light source (108). A first sensor processing module (112) may derive blood oxygen saturation using sensed photo-acoustic signals (114). A second sensor processing module (116) may derive blood core temperature using sensed photo-acoustic signals. A third sensor processing module (118) may derive blood glucose using sensed photo-acoustic signals. The sensing apparatus is configured to derive at least one of: a de-correlated value (120) of blood oxygen saturation of the subject; a de-correlated value (122) of blood core temperature of the subject; and a de-correlated value (124) of blood glucose of the subject.

Abstract: An apparatus and method of assessing a narrowing in a fluid filled tube having a fluid flow pressure wave having a backward-originating pressure component and a forward-originating pressure component without taking a flow velocity measurement, comprising: taking pressure measurements in the tube; separating the pressure components into the backward-originating pressure component and the forward-originating pressure component; identifying a time window when the differential of flow velocity (dU) is minimal or absent; and deriving the backward and forward pressure components for pressure measurements taken in at least the time window.

Abstract: A biological information monitor includes: a measuring section which is configured to measure biological information having a periodically changing value; a sound outputting section which is configured to output a sound including a first sound and a second sound, in synchronization with a period of the biological information; and a sound controlling section which is configured to cause the second sound to be output in succession to the first sound, and which is configured to change the second sound in accordance with a value of the biological information.

Abstract: A hemodynamic parameter (Hdp) monitoring system for diagnosing a health condition of a patient and for establishing Hdp marker values or Hdp surrogate marker values for purposes of comparison with Hdp values of a patient is provided. An Hdp monitor senses, measures, and records Hdp values exhibited by the patient during a basal or non-exposure period and furthermore Hdp values exhibited by the patient during or after an exposure period during which the patient is exposed to low-energy electromagnetic output signals. An electrically-powered generator is adapted to be actuated to generate said low-energy electromagnetic carrier output signals for exposing or applying to the patient such output signals during said exposure period.

Abstract: Devices and systems described herein relate to a sensing device that includes an output area and an electrode area. The output area includes an output circuit comprising an integrator adapted to integrate a received current so as to generate an output voltage corresponding to the received current. The electrode area includes an electrode comprising an exposed, electrically conductive, surface area and electrode circuitry connected to the exposed surface area. The electrode circuitry comprises a voltage-to-current transducer adapted to produce a wire current corresponding to a voltage present at the exposed surface area. The sensing device also includes a connecting wire electrically connecting the electrode circuitry to the output circuit, wherein the current received by the output circuit is the wire current.

Abstract: An electrode assembly includes a needle and a conductive thread electrode carried in a slot on the surface of the needle. The needle pushes the thread electrode into the body and leaves it in place when the needle is removed. The needle is secured in a housing in a retracted position and moved to an extended position by a latch. In the extended position, one end of the needle remains in the housing and the other end extends from the housing. The needle is attached to a spring inside the housing and is moved by the latch against the urging of the spring to the extended position and locked in place. A protective cover is applied over the needle while extended and removed to insert the needle into the body of a patient.

Abstract: A handheld electrocardiographic measurement device includes a substantially spheroidal body, a stopper projecting along an axial direction of the body to restrict a position of a thumb of one hand by abutting on a side surface of the thumb when a user grips the body with the one hand, a plate-shaped flange projecting from a side surface of the body in a direction orthogonal or substantially orthogonal to a projecting direction of the stopper, a first electrocardiographic electrode disposed on a back side of the body to touch a finger of the one hand when the body is gripped with the one hand, and a second electrocardiographic electrode disposed on a surface of the flange to touch a finger of the other hand when the flange is pinched by the other hand.

Abstract: The present disclosure generally relates to user interfaces for health monitoring. Exemplary user interfaces for initial setup of health monitoring using a first electronic device and a second electronic device is described. Exemplary user interfaces for recording biometric information for use in health monitoring is described. Exemplary user interfaces for using an input device while recording biometric information for health monitoring is described. Exemplary user interfaces for viewing and managing aspects of health monitoring is described.

Abstract: Long-term electrocardiographic and physiological monitoring over a period lasting up to several years in duration can be provided through a continuously-recording subcutaneous insertable cardiac monitor (ICM). The sensing circuitry and the physical layout of the electrodes are specifically optimized to capture electrical signals from the propagation of low amplitude, relatively low frequency content cardiac action potentials, particularly the P-waves that are generated during atrial activation and storing samples of captured signals. In general, the ICM is intended to be implanted centrally and positioned axially and either over the sternum or slightly to either the left or right of the sternal midline in the parasternal region of the chest.

Abstract: A method for constructing physiological electrode assembly with integrated flexile wire components is provided. A flexible backing is formed from a stretchable woven textile material, the flexible backing having a proximal flexible backing end and a distal flexible backing end. A set of flexile wires is integrated into the proximal flexible backing end to form a set of electrical contact surfaces shaped to interface with a monitor recorder on a side of proximal electrical backing end opposite the contact side of the proximal flexible backing end. An electrocardiographic electrode is positioned on the contact side of the distal flexible backing end. A further electrocardiographic electrode is positioned on the contact side of the proximal flexible backing end. One of the electrical contact surface of the set of electrical surfaces is connected to the electrocardiographic electrode.

Abstract: A method of mapping includes receiving inputs measured by a probe at respective locations inside a body cavity of a subject. At each of the respective locations, a respective contact quality between the probe and a tissue in the body cavity is measured. The inputs for which the respective contact quality is outside a defined range are rejected, and a map of the body cavity is created using the inputs that are not rejected.

Abstract: A catheter may be adapted to map a chamber of the heart. The catheter may include a magnetic and/or ultrasound sensor for navigation. The body of the catheter may be pliable and configured to form a predetermined shape upon exiting a catheter sheath. Upon exiting the catheter sheath, the catheter body may be configured to form one or more loops, and the loops may be non-overlapping loops. In some examples, the non-overlapping loops may be concentric loops. Alternatively, the catheter body may be configured to form one or more splines. The catheter body may include an embedded electrode assembly. The electrodes of the electrode assembly may be may be arranged in one or more rows and configured to detect a wave front. The electrode assembly may also be configured to generate and activation sequence and determine a direction of an activation source.

Abstract: A myocardial excitation complementation/visualization apparatus includes an acquiring section that acquires intracardiac electrocardiograms of a subject, the intracardiac electrocardiograms being recorded by a recording unit having a plurality of electrodes, a processing section that performs a computation for completing and visualizing a state of excitation in a myocardium of the subject based on the intracardiac electrocardiograms, and a displaying section that displays the state of excitation in the myocardium of the subject based on an output of the processing section. The processing section includes a first generating section, a correcting section, a second generating section, and a third generating section. The displaying section displays a change of the state of excitation in the myocardium of the subject based on the visualized data.

Abstract: A medical imaging system and method is described. The system comprises: a microwave antenna array comprising a transmitting antenna and a plurality of receiving antennae, wherein the transmitting antenna is configured to transmit microwave signals so as to illuminate a body part of a patient and the receiving antennae are configured to receive the microwave signals following scattering within the body part; a marker configured to be applied to the surface of the skin of the body part and to scatter the microwave signals; a processor configured to process the scattered microwave signals and generate an image of the internal structure of the body part and the marker so as to identify a region of interest within the body part relative to the position of the marker.

Abstract: An electrophysiology map, for example a map of arrhythmic substrate, can be generated by acquiring both geometry information and electrophysiology information pertaining to an anatomical region, and associating the acquired geometry and electrophysiology information as a plurality of electrophysiology data points. A user can select two (or more) electrophysiological characteristics for display, and can further elect to apply various filters to the selected electrophysiological characteristics. The user can also define various relationships (e.g., Boolean ANDS, ORs, and the like) between the selected and/or filtered characteristics. The user-selected filtering criteria can be applied to the electrophysiology data points to output various subsets thereof. These subsets can then be graphically rendered using various combinations of colorscale, monochrome scale, and iconography, for example as a three-dimensional cardiac electrophysiology model.

Abstract: Systems and methods are provided for generating a protocol independent image. A deep learning generative framework learns to recognize the boundaries and classification of tissues in an MRI image. The deep learning generative framework includes an encoder, a decoder, and a discriminator network. The encoder is trained using the discriminator network to generate a latent space that is invariant to protocol and the decoder is trained to generate the best output possible for brain and/or tissue extraction.

Abstract: Various embodiments of a fall prediction system and method of using such system are disclosed. The system includes a hearing device for a wearer, a sensor operatively connected to the hearing device and adapted to detect a characteristic of the wearer and generate a sensor signal based on the characteristic, and a controller operatively connected to the hearing device. The controller is adapted to determine a fall risk value based on the sensor signal, compare the fall risk value to a fall risk threshold, and generate a fall prevention output if the fall risk value exceeds the fall risk threshold.

Abstract: An electronic device (1) includes: a positional information obtaining section (21) for obtaining positional information; a boarding determining section (12) for determining whether or not a user has boarded or exited a vehicle; and a frequency switching section (14) for switching a frequency, at which the positional information is obtained, from a first frequency to a second frequency in a case where it is determined that the user has boarded or exited the vehicle.

Abstract: Techniques for user identification by a biometric monitoring device are disclosed. In one aspect, a method of operating a biometric monitoring device may involve measuring a weight of a user in response to detecting that the user is standing on a platform, determining, based on sensor data generated by a sensor, a user parameter indicative of the user's identification, identifying one of a plurality of user profiles as corresponding to the user based on a comparison of the user parameter to parameter values and a comparison of the measured weight of the user to weight values, and updating the identified user profile based on at least one of the measured weight and the user parameter.

Abstract: Certain embodiments provide a hearing testing probe apparatus. The hearing testing probe apparatus includes a probe tube detachably coupled at a first end to a probe body and extending through a center hole in an eartip to align proximate a face of the eartip at a second end. The probe tube includes a plurality of stimulus lumens for receiving and carrying stimulus from the first end of the probe tube for output at the second end of the probe tube. The probe tube includes one or more microphone lumens for receiving and carrying one or more measured responses from the second end of the probe tube to one or more microphones at the first end of the probe tube.

Abstract: The present disclosure relates to noninvasive methods, devices, and systems for measuring various blood constituents or analytes, such as glucose. In an embodiment, a light source comprises LEDs and super-luminescent LEDs. The light source emits light at at least wavelengths of about 1610 nm, about 1640 nm, and about 1665 nm. In an embodiment, the detector comprises a plurality of photodetectors arranged in a special geometry comprising one of a substantially linear substantially equal spaced geometry, a substantially linear substantially non-equal spaced geometry, and a substantially grid geometry.

Abstract: The present disclosure relates to noninvasive methods, devices, and systems for measuring various blood constituents or analytes, such as glucose. In an embodiment, a light source comprises LEDs and super-luminescent LEDs. The light source emits light at at least wavelengths of about 1610 nm, about 1640 nm, and about 1665 nm. In an embodiment, the detector comprises a plurality of photodetectors arranged in a special geometry comprising one of a substantially linear substantially equal spaced geometry, a substantially linear substantially non-equal spaced geometry, and a substantially grid geometry.

Abstract: An oximeter probe includes sensor head with a probe face having one or more sensor structures to make measurements, a handle, and an elastic member connected between the handle and the base. A user can hold the handle while measurements are made and the elastic member permits the handle to flex relative to the sensor head with one or more sensor structures.

Abstract: 3D microscale metamaterial structures and methods of making. The metamaterial structure includes a polygonal structure having a plurality of panels connected to one another at structure corners. A metal resonator pattern is provided on each of the panels. The resonator patterns of neighboring panels are electromagnetically coupled to one another across a gap between the resonator patterns at the corresponding structure corner. The panels can be a polymer material, layers of graphene oxide, etc. The metamaterial structure can be a 3D octagram split-ring resonator, and is completely isotropic. The 3D metamaterial structure can be made by a self-folding process.

Abstract: Provided are dermal sensors and dermal sensor applicator sets to insert at least a portion of a dermal sensor into a dermal layer of a subject, as well as methods of making and using the same.

Abstract: Systems and methods for processing sensor data and self-calibration are provided. In some embodiments, systems and methods are provided which are capable of calibrating a continuous analyte sensor based on an initial sensitivity, and then continuously performing self-calibration without using, or with reduced use of, reference measurements. In certain embodiments, a sensitivity of the analyte sensor is determined by applying an estimative algorithm that is a function of certain parameters. Also described herein are systems and methods for determining a property of an analyte sensor using a stimulus signal. The sensor property can be used to compensate sensor data for sensitivity drift, or determine another property associated with the sensor, such as temperature, sensor membrane damage, moisture ingress in sensor electronics, and scaling factors.

Abstract: A blood glucose test strip includes a test strip, a blood test area formed on a first end of the test strip, an electrode formed on a second end of the test strip, a data barcode formed on the test strip, and a clock code formed on the test strip. The data barcode may include a plurality of first bars with spaces separating the first bars, each first bar having a width. The clock code may comprise a fixed pattern of second bars with spaces separating the second bars, a width of each second bar set according to the width of at least one of the first bars. The clock code can be used to calibrate the data barcode to compensate for insertion speed and/or moisture content.

Abstract: The disclosed embodiments include user fatigue level analysis components, real-time visual behavior measuring devices, and methods for determining the fatigue level of a user. In one embodiment, a user fatigue level analysis component includes a memory configured to store computer executable instructions and a processor for executing the computer executable instructions. The computer executable instructions comprise instructions for receiving at least a visual behavior parameter indicative of the real time visual behavior of the user, for providing at least one sleep quality history parameter indicative of the sleep quality history of the user, and for determining the fatigue level of the user based on the analysis of the combination of the at least one visual behavior parameter and the at least one sleep quality history parameter.

Abstract: A device to monitor penetration of an instrument in an anatomical structure including at least two electrodes, a source of current supplying the at least two electrodes, and means for measuring impedance between the electrodes, wherein the electrodes are located on the penetration instrument, wherein the first electrode has a contact surface coinciding with a distal surface of the penetration instrument and the second electrode has a contact surface coinciding with a lateral surface of the penetration instrument, and wherein the contact surfaces are dimensioned to have a coinciding and constant contact surface as a function of a degree of penetration of the penetration instrument in the anatomical structure.

Abstract: There is a sunscreen detection device for detecting a sunscreen product, the sunscreen detection device comprising: a substrate; a first light, disposed on the substrate and controllably coupled to a processor, controllable by the processor to emit light at a first light wavelength at the subject's skin when the sunscreen detection device is oriented to emit light on the subject's skin; a first light sensor circuit, disposed on the substrate and communicatively coupled to the processor, capable of sensing a percentage absorption of light by the subject's skin at the first light wavelength (% AbsAtWL1) and communicating the % AbsAtWL1 to the processor; a processor, configured to: cause the first light to emit light when the sunscreen detection device is oriented to emit light on the subject's skin; record the % AbsAtWL1 from the first light sensor; and assess a level of sunscreen protection based at least on the % AbsAtWL1.

Abstract: The present invention relates to a determination system, a corresponding determination method and a computer program for determining a sleep stage of a subject. The determination system comprises a cardiorespiratory signal providing unit (10), an actigraphy data providing unit (20), a first sleep stage determination unit (30) for determining the sleep stage based on a cardiorespiratory signal, and a second sleep stage determination unit (40) for determining the sleep stage based on actigraphy data. The first sleep stage determination unit (30) determines a sleep onset latency (SOL) of the subject. The sleep stage of the subject is determined using the first sleep stage determination unit (30) up to the SOL and the second sleep stage determination unit (40) after the SOL. The determination system and corresponding method allow for a more reliable determination of a sleep stage of subject, in particular improve the determination of the SOL of the subject.

Abstract: A method, a wearable device, and an apparatus for monitoring sleep of a user are provided. The method includes: determining an activity amount of a user based on multi-axial acceleration data received by the wearable device in a time period, in which the multi-axial acceleration data includes acceleration data in multiple axes; if the activity amount is smaller than a first threshold, determining a microactivity feature value using the multi-axial acceleration data and predetermined weights; and determining a microactivity state for the user in the time period based on the microactivity feature value, in which the activity amount of the user is substantially zero in the microactivity state.

Abstract: A device for use in the medical and hospital sector for the diagnosis, induced regeneration of tissue by means of therapeutic percutaneous electrolysis and targeted electro-stimulation based on the use of at least one bipolar needle that includes within a very small area of two electrodes located at the exterior and interior conductor of said bipolar needle, limiting the tissue to be treated within the bevel area of the needle without affecting the surrounding healthy tissue in which said bipolar needle is applied the necessary electrical signals for diagnosing the degree of degeneration and to calculate the necessary electrical charge for treating the damaged tissue while controlling said current in a manner that eliminates the contraindications that currently exist.

Abstract: Systems, methods and/or devices for treating diabetes mellitus by alleviating glucotoxicity and restoring pancreatic beta-cell function, comprising at least a first memory for storing data inputs corresponding at least to one or more components in a patient's present insulin dosage regimen, and data inputs corresponding at least to the patient's blood-glucose-level measurements determined at a plurality of times, and a processor operatively connected to the at least first memory. The processor is programmed at least to determine from the data inputs corresponding to the patient's blood-glucose-level measurements determined at a plurality of times whether and by how much to vary at least one of the components of the patient's present insulin dosage regimen.

Abstract: In embodiments, devices, methods and systems to analyze the different mediums of brain function in a mathematically uniform manner may be provided. These devices, methods and systems may manifest at several levels and ways relating to brain physiology, including neuronal activity, molecular chirality and frequency oscillations. For example, in an embodiment, a computer-implemented method for determining structure of living neural tissue may comprise receiving at least one signal from at least one read modality, the signal representing at least one physical condition of the living neural tissue, determining action potentials based on the signals received from the read modalities, determining frequency oscillations based on the signals received from the read modalities and the action potentials, and determining neuron network structures based on the signals received from the read modalities, the action potentials, and the frequency oscillations.

Abstract: A biofeedback system for monitoring patient-related signals of a patient having adolescent idiopathic scoliosis (AIS) is disclosed. The present invention provides a personalized biofeedback to the patient based on the patient-related signals for restoring balance in muscle activities and reducing displacement of both sides of the patient's spine as a treatment for AIS. The biofeedback system comprises clothing integrated with posture monitoring sensors, and one or more computational systems comprising a sensor-based sEMG posture training subsystem for providing posture training and a posture monitoring subsystem for providing progressive training through daily activities. The sensor-based sEMG posture training subsystem comprises a posture training device coupled to a plurality of sEMG sensors, a feedback device and a calibration system.

Abstract: A vital signs monitoring system comprises a processing unit (300) for estimating an activity energy expenditure (AEE), a first activity energy expenditure determining unit (320) for determining a first activity energy expenditure (AEEHR) based on heart rate data (HR), a second activity energy expenditure determining unit (330) for determining a second activity energy expenditure (AEEAC) based on motion data (AC), and a weighting unit (340) for determining a first and second weighting factor (wHR, wAC) based on a first and second probability relating to a high exertion (hH) and relating to a low exertion (hL), and activity energy expenditure calculating unit (350) for computing an overall activity energy expenditure (AEEO) based on the first activity energy expenditure (AEEHR) weighted by the first weighting factor (wHR) and on the second activity energy expenditure (AEEAC) weighted by the second weighting factor (wAC).

Abstract: A bio-information acquiring terminal for acquiring bio-information includes a bath device. The bath device is provided with a bio-information measuring unit configured to measure bio-information of a user taking a bath, and a fingerprint authentication unit configured to specify the user. According to the above configuration, it is possible to easily manage daily changes of the health condition of the user in his or her daily life.

Abstract: An electronic skin is manufactured by disposing an oxide thin film transistor (TFT), a pressure sensor, and a temperature sensor on a flexible substrate. The pressure sensor and the temperature sensor are respectively located on two sides of the flexible substrate. The oxide TFT includes a first TFT and a second TFT. The pressure sensor is configured to drive the first TFT, and the temperature sensor is configured to drive the second TFT. The method for preparing the electronic skin is to form an oxide TFT, a pressure sensor, and a temperature sensor by means of etching and deposition on a flexible substrate whose double sides are covered with conductive materials. The electronic skin provided in the present invention may simultaneously measure pressure and temperatures, and has a simple structure, a low working voltage, small power consumption, high sensitivity, and small interference between sensor signals.