The invention relates to a measurement device 1 comprising a rotatable magnetic object 4 which can oscillate with a resonant frequency if excited by an external magnetic torque. The measurement device 1 is adapted such that the resonant frequency depends on the temperature or on another physical or chemical quantity like pressure, in order to allow for a wireless temperature measurement or measurement of the other physical or chemical quantity via an external magnetic field providing the external magnetic torque. This measurement device can be relatively small, can be read-out over a relatively larger distance and allows for a very accurate measurement.

Disclosed herein are devices, systems, and methods for updating alarm limits applied in monitoring one or more medical parameters of a subject. The devices, systems, and methods obtain a measurement of ambient pressure at a defined time point (‘t.sub.1’) and compare the measurement of ambient pressure at the defined time point (‘t.sub.1’) to a reference ambient pressure. If a difference between the measured ambient pressure values at t.sub.1 and the reference ambient pressure is at or above a predetermined threshold, the alarm limits are updated to correspond with the ambient pressure at t.sub.1 or a user is alerted to update the alarm limits.

Introduced are a bed device system and methods for: gathering human biological signals, such as heart rate, breathing rate, or temperature; analyzing the gathered human biological signals; and controlling the bed device system, e.g., a temperature of the bed device, based on the analysis.

A monitoring and/or therapy apparatus can include a contact layer having a stretchable or substantially stretchable substrate, at least one strain sensor coupled with the contact layer, and electronic circuitry electronically coupled with the at least one strain sensor configured to determine an amount of an elongation of the at least one strain sensor based on a change in a resistance or capacitance of the at least one strain sensor. The at least one strain sensor can include a plurality of stretchable tracks positioned on the substrate, and can be configured such that the resistance of the at least one strain sensor increases as the contact layer is elongated and/ or curved. In some arrangements, the apparatus and/or the substrate can be attached to or adjacent to a user’s joint, and/or a wound, and can be configured to have reduced pressure applied to the space under the contact layer..

A wearable blood pressure meter includes a semi-conformable bladder, serving as a reservoir for an incompressible fluid, and a pressure sensor. The semi-conformable bladder includes a rigid housing defining a cavity within which the incompressible fluid is rigidly constrained and an elastic membrane for elastically constraining the incompressible fluid. The elastic membrane extends across an aperture into the cavity through the rigid housing. The elastic membrane conforms to a body part at the aperture when pressed against the body part. The pressure sensor mechanically couples to the incompressible fluid to measure pressure signals emanating from an artery within the body part and which propagate through the conformable membrane and the incompressible fluid to the pressure sensor.

A wearable sensor device includes a temperature and humidity sensor that measures ambient environmental information around a living body, a snap button connected to a bioelectrode, a biological information measurement unit that measures biological information, an inertial sensor that measures inertial information, a calculation unit that calculates a biological feature amount based on the biological information and calculates an inertial feature amount based on the inertial information, and a wireless communication unit that transmits the biological information, the inertial information, the biological feature amount, the inertial feature amount, and the environmental information to the outside.

A trained model running on a wearable device can be used to analyze PPG inputs and error/confidence levels, internal and/or external temperature inputs, and motion sensor data to determine whether the wearable device can be more tightly secured to the body of a user to improve PPG or other health sensor signals. A clustering model can be used to analyze data in real time or close to real time, and provide a notification to the user. The notifications can indicate steps to be taken to improve the signal quality from the wearable device, such as tightening the device.

A garment with safety features is described. The garment includes a covering configured to cover at least a portion of a wearer. The covering extends between a first location and a second location spaced apart from the first location. The garment includes a flexible panel with the covering overlaying the flexible panel. The flexible panel is attached to the covering at the first location and the second location. The covering comprises excess material between the first location and the second location, the excess material being configured to accommodate stretching of the flexible panel.

An apparatus for energy expenditure estimation includes a heart rate sensor for producing a heart rate value indicative of a heart rate of an individual, a heat-flux sensor for producing a heat-flux value indicative of a heat-flux flowing through a measurement area on the skin of the individual, and a processing system communicatively connected to the heart rate sensor and the heat-flux sensor. The processing system is configured to produce an estimate of the energy expenditure based on the heart rate value and the heat-flux value. The use of the heat-flux value improves the accuracy of the estimation especially during low-intensity exercise and rest, when both heart rate and acceleration values often fail to provide information meaningful enough for energy expenditure estimation.

Disclosed is a breath sampling device comprising a buffer tube, sensor module and breath sampling port. The buffer tube has a proximal end into which a user exhales and a distal end opposite the proximal end, the sensor module is at the distal end and used for measuring parameters of a breath exhaled by the user into the buffer tube, and the breath sampling port is disposed between the proximal end and distal end. The used exhales into the distal end and a portion of the exhaled breath can be diverted into the sampling port substantially without contacting the sensor module.