Abstract: An on-body sensing system (30) comprises a plurality of skin interface elements for coupling electrical signals to and from the body. The system is adapted to derive an indication of a position of at least one positionable interface unit (32) based on transmission of signals between the positionable unit and a set of spatially separated reference units (34), the reference units being positioned at a set of known locations on the body. Transmitted signals are sensed at multiple pairs (52) of electrodes on each reference unit and signal characteristics derived for each pair, and based on this a direction of arrival of the signal determined. By collating all of the measured arrival angles, and by reference to a reference dataset containing information indicative of known signal arrival angles when signals are transmitted internally between the reference units themselves, an indication of position of the positionable unit is derived.

Abstract: Provided are a temperature measurement apparatus, a biometric detection assembly, and a wearable device. The temperature measurement apparatus comprises a housing, a temperature measurement component and an elastic component. The temperature measurement component is used for measuring the temperature of a measured object. The temperature measurement component can move relative to the housing, and the elastic component is arranged between the housing and the temperature measurement component.

Abstract: A system comprises a first sensor for generating a swelling signal based on the user pressing on the first sensor with a body part, a second sensor for generating a blood signal which is indicative of the volume of blood in the body part when the user presses on the first sensor and a force sensor for measuring the force applied by the body part to the first sensor when the user presses on the first sensor. The system also comprises a processor configured to determine an indication of swelling for the body part based on the swelling signal when the force sensor measures a first pre-determined value, determine an indication of blood pressure at the body part based on a force value measured by the force sensor when the blood signal reaches a second pre-determined value.

Abstract: A sensing system and method uses a sense electrode arrangement for coupling to a surface of a body such that the sense electrode arrangement and the body (and the spacing between them) define a coupling capacitance. First and second sensing circuits have different transfer functions and generate first and second outputs. These outputs are processed to determine the coupling capacitance. The electrophysiological signal being monitored is also acquired by one or both of the sensing circuits. In this way, the quality of the electrode coupling can be determined in a simple and passive manner.

Abstract: A method for determining a health status of a system of interest is proposed. The method comprises acquiring (S1) a time series, extracting (S2) subsequences, selecting (S3) a set of subsequences, classifying (S4) the subsequences of the set into several groups on the basis of at least one criterion of resemblance to at least one reference subsequence, and constructing (S5) a normal operating model of the system of interest. The construction includes, for each group, a modeling (S51) of a representative subsequence and a determination (S52) of an associated weight. The normal model is defined by the modeled subsequences and the associated weights. The method further includes an attribution (S6) of a normality score to each subsequence extracted by comparison with the normal model, an identification (S7) of at least one abnormal subsequence, and a determination (S8) of the health status of the system of interest.

Abstract: An on-body sensor system (30) comprises at least two skin interface units (32, 34) for coupling signals into and out of the body, with one of the units being for placement at a known location. One unit applies electrical signals to the body and the other senses them at a remote location. By analyzing the sensed signals using a set of pre-determined body-transmission parameters, a position of one of the skin interface units can be determined. This allows accurate placement of one or the units, for instance to allow more accurate monitoring of physiological parameters using the unit. The body transmission parameters can change over time, whereas once the interface units are put in position, their position is stable. Hence the system also includes functionality to re-calibrate the transmission parameters using at least one known stable set of initial positions of the interface units. The re-calibration comprises a process of re-calculating the parameters based on the known positions.

Abstract: An on/in-body communication system (10) is described that may include a peripheral, (such as, for example portable, unit (12)) and body-mountable unit (20). The peripheral unit and body-mountable unit may communicate via body-coupled acoustic signals. This may facilitate secure transmission of a secure key from the peripheral unit to the body-mountable unit. The body-mountable unit may include an array (28) of acoustic sensor elements (30) disposed at a body-coupling surface (32) of the body-mountable unit for receiving a transmitted acoustic signals, the array formation facilitating multi- or omni-directional sensing. A key may be transferred in an initialization procedure which may include establishing communications with an external device (42) via an off-body communication medium, acquiring from the external device a secure key, and/or driving acoustic transmission of the secure key to the body-mountable device via an acoustic signal generator (14).

Abstract: A method for determining a health status of a system of interest is proposed. The method comprises acquiring (S1) a time series, extracting (S2) subsequences, selecting (S3) a set of subsequences, classifying (S4) the subsequences of the set into several groups on the basis of at least one criterion of resemblance to at least one reference subsequence, and constructing (S5) a normal operating model of the system of interest. The construction includes, for each group, a modeling (S51) of a representative subsequence and a determination (S52) of an associated weight. The normal model is defined by the modeled subsequences and the associated weights. The method further includes an attribution (S6) of a normality score to each subsequence extracted by comparison with the normal model, an identification (S7) of at least one abnormal subsequence, and a determination (S8) of the health status of the system of interest.

Abstract: Disclosed is a vital sign monitoring system. The system comprises a segmented electrode forming an in-plane electrode array, wherein the electrode comprise a skin contacting skin adhering contact layer mounted on an electrode backing material, a deformation sensor arranged for identifying deformation information of the electrode, a signal processor arranged to receive a vital sign signal from the electrode and process the deformation information to remove artefacts from the vital sign signal, wherein the electrode comprises multiple electrode segments and wherein the signal processor is arranged to select that electrode segment that has a lowest deformation of all electrode segments of the electrode.

Abstract: An on-body sensing system (30) comprises a plurality of skin interface elements for coupling electrical signals to and from the body. The system is adapted to derive an indication of a position of at least one positionable interface unit (32) based on transmission of signals between the positionable unit and a set of spatially separated reference units (34), the reference units being positioned at a set of known locations on the body. Transmitted signals are sensed at multiple pairs (52) of electrodes on each reference unit and signal characteristics derived for each pair, and based on this a direction of arrival of the signal determined. By collating all of the measured arrival angles, and by reference to a reference dataset containing information indicative of known signal arrival angles when signals are transmitted internally between the reference units themselves, an indication of position of the positionable unit is derived.

Abstract: There is provided a method and apparatus for determining at least one of a position and an orientation of a wearable device on a subject. At least one physiological characteristic signal is acquired from a subject (402). The acquired at least one physiological characteristic signal from the subject has one or more characteristics indicative of at least one of a position and an orientation of a wearable device on the subject. The at least one of the position and orientation of the wearable device on the subject is determined based on the one or more characteristics indicative of the at least one of the position and orientation of the wearable device on the subject (404).

Abstract: A system is provided for determining the position of an implanted device (10) in a human or animal body relative to a probe (12). In one device, a reference signal is generated and it is received in the other device. A phase angle or an amplitude attenuation or difference between the reference signal and the received signal is used to determine the proximity the probe to the implanted device. The approach makes use of body channel sensing by which the frequencies at which the body behaves as a waveguide are employed.

Abstract: A wearable device for continuous health monitoring, the device comprising: a band for conforming to a first body part of a subject; an imaging unit, the imaging unit being connected in the band, wherein the imaging unit is configured to acquire a sequence of images from the subject's body, wherein the device is operable in a contact mode and in a non-contact mode, i.

Abstract: Disclosed is a vital sign monitoring system. The system comprises a segmented electrode forming an in-plane electrode array, wherein the electrode comprise a skin contacting skin adhering contact layer mounted on an electrode backing material, a deformation sensor arranged for identifying deformation information of the electrode, a signal processor arranged to receive a vital sign signal from the electrode and process the deformation information to remove artefacts from the vital sign signal, wherein the electrode comprises multiple electrode segments and wherein the signal processor is arranged to select that electrode segment that has a lowest deformation of all electrode segments of the electrode.

Abstract: There is provided a wearable device operable to determine an orientation of the wearable device, when placed on a body. The wearable device comprises a plurality of electrode pairs located at different positions. At least two of the plurality of electrode pairs are configured to receive a signal transmitted from a reference device using the body as a transmission medium. The wearable device also comprises a processor configured to determine a property associated with the signal received at the at least two electrode pairs, compare the determined property to a corresponding reference property and determine, from the comparison, whether the wearable device is in the predetermined orientation on the body. The determined property is indicative of an orientation of the wearable device with respect to the reference device and the corresponding reference property is indicative of a predetermined orientation for the wearable device on the body.

Abstract: There is provided a method and apparatus comprising a processor to provide guidance for placement of a wearable device. At least one image of the body of a subject is acquired from one or more cameras (502). The at least one acquired image is analysed to recognise body parts of the subject and to identify a body part of the subject at which to place the wearable device (504). Guidance to place the wearable device at the identified body part of the subject is provided (506).

Abstract: Various methods and apparatus for a wearable or insertable device (100, 200, 400, 600) with microneedles (106, 206, 306, 406, 606) that may be simultaneously used for radio frequency (RF) energy harvesting, communication, and transdermal fluid delivery and collection are disclosed. Such a device may comprise a substrate (102, 202, 302, 402, 602) that may be affixable/insertable into tissue (107, 607) of a patient, radio frequency circuitry (120, 220, 420, 620) disposed on the substrate, that may generate/process a signal with a frequency that may be modulated to carry information, and microneedles (106, 206, 306, 406, 606) extending from at least one surface of the substrate, where one or more microneedles define a micro-fluidic channel (130, 230, 430, 630) that fluidly couples the tissue with a conduit (132) of the substrate, and where one or more microneedles may be electrically coupled with the radio frequency circuitry and radiate/process electromagnetic waves based on the signal.

Abstract: There is provided a method and apparatus for determining at least one of a position and an orientation of a wearable device on a subject. At least one physiological characteristic signal is acquired from a subject (402). The acquired at least one physiological characteristic signal from the subject has one or more characteristics indicative of at least one of a position and an orientation of a wearable device on the subject. The at least one of the position and orientation of the wearable device on the subject is determined based on the one or more characteristics indicative of the at least one of the position and orientation of the wearable device on the subject (404).

Abstract: A method of preventing or suppressing a false alarm during administration of food or medicine to a human or animal through a feeding tube having one or more sensors that generate a signal, comprises analyzing the signals to determine whether food or medicine is being administered and, if it is determined that food or medicine is present, preventing or suppressing an alarm. In a further step, the time and length of administration of food or medicine is recorded. When the feeding tube has at least two temperature sensors, differences in the temperatures recorded for the different temperature sensors indicate that food or medicine was administered. In a case where there is only one temperature sensor, the rate and extent of any temperature change of temperatures recorded from that temperature sensor are compared to an algorithm to determine whether feeding occurred.

Abstract: A wearable device for continuous health monitoring, the device comprising: a band for conforming to a first body part of a subject; an imaging unit, the imaging unit being connected in the band, wherein the imaging unit is configured to acquire a sequence of images from the subject's body, wherein the device is operable in a contact mode and in a non-contact mode, i.