A conventional flow tube for a metabolic cart is usually a straight length of pipe whose inner diameter is fixed by the respiratory burden imposed by the flow tube on the user, with a smaller diameter imposing a higher respiratory burden. The ratio of the straight flow tube's length to diameter is fixed by fluid dynamics, so increasing the flow tube's diameter causes the flow tube's length to increase. As the flow tube gets longer, it exerts more torque on the user's neck and jaw, creating discomfort. Reducing the flow tube's length causes an undesired increase in the respiratory burden but increasing the flow tube's diameter to reduce the respiratory burden makes the flow tube less comfortable, making the flow tube unconformable, hard to breathe through, or both. Bending the flow tube makes it possible to increase the flow tube's propagation length without increasing the flow tube's lever arm length.

The disclosed wearable may include (1) a plurality of electrodes dimensioned to interface with a skin surface of a user of an artificial reality system, wherein the electrodes are spaced a known distance from one another, (2) a signal generator communicatively coupled to one of the electrodes, wherein the signal generator injects a test signal into the skin surface of the user via the one of the electrodes, (3) at least one sensor communicatively coupled to another one of the electrodes, wherein the sensor measures the test signal as received by the another one of the electrodes, and (4) at least one processing device communicatively coupled to the sensor, wherein the processing device determines a current impedance of the skin surface based at least in part on the known distance and the measurement of the test signal. Various other systems and methods are also disclosed.

An electronic device is provided. The electronic device includes a biometric sensor for detecting biometric data, a situation sensing module, memory, and a processor operatively coupled to the biometric sensor, the situation sensing module, and the memory. The processor can check whether a user is in an inactive state using the situation sensing module, check reference biometric data corresponding to the inactive state if the user is in the inactive state, extract biometric data of the user using the biometric sensor, and measure the blood pressure of the user on the basis of the extracted biometric data and the reference biometric data.

A method for creating calibration data for processing accelerated measurement data of an object to be examined using a magnetic resonance system. The method includes recording measurement data sets using an acquisition acceleration method, recording calibration data sets, and determining processed measurement data sets from the accelerated measurement data sets using the calibration data sets so that effects of the acquisition acceleration method used are eliminated in the processed measurement data sets. The recording of the calibration data sets includes an application of at least one attenuation method for attenuating signals causing phase errors.

Methods and systems for determining the blood pressure of a patient. The system may include a first device configured to collect a first plurality of blood pressure measurements of the patient, a second device configured to collect a second plurality of blood pressure measurements of the patient, and a processor configured to identify a divergence between the first plurality and the second plurality, retrieve, from a memory, a clinical event, compare the first plurality and the second plurality to the clinical event, and determine that the first plurality is more accurate than the second plurality based on the comparison.

A method includes receiving, from a first sensor, first physiological data associated with a first sleep session of a user. The method also includes receiving, from a sensor, second physiological data associated with a first sleep session of a user. The method also includes determining a first set of sleep-related parameters associated with the first sleep session of the user based at least in part on the first physiological data. The method also includes determining a second set of sleep-related parameters associated with the first sleep session of the user based at least in part on the second physiological data. The method also includes calibrating the second sensor based at least in part on a comparison between the first set of sleep-related parameters and the second set of sleep-related parameters.

A method for performing an eye test includes the steps of: receiving a request from a user to perform the eye test; acquiring predetermined user identification data from the user; presenting or providing at least one test image to the user, the at least one test image including at least one test target contained therein; instructing the user to identify at least one of the at least one test target(s) contained within the at least one test image; acquiring response data associated with the user's attempt(s) to identify the at least one test target(s) contained within the at least one test image; aggregating and/or analysing the acquired user identification data and/or the response data utilising a test algorithm which determines result data; and, presenting or providing the result data to the user.

An optical analyte sensor and diabetes management system is provided. The sensor preferably includes a hydrogel matrix for receiving a sample containing an analyte at unknown concentration, a light emitter for emitting light at a stimulation frequency, a light receiver for receiving a fluorescence signal at a first isosbestic frequency, and at a second frequency, for measuring an intensity of the fluorescence signal and the first and second frequencies. A processor determines a concentration of the analyte based on the respective intensities.

An optical fiber blood pressure continuous detection wristband, comprising: an optical fiber sensing assembly module, the optical fiber sensing assembly module includes a sensing band and an optical fiber configured to extend along the sensing band and form a sensing area to sense a pulse wave; the sensing band includes an inner layer configured to be placed adjacent to the wrist to be detected, and the outer surface of the inner layer is abutted against the optical fiber; an outer layer, the inner surface of the outer layer is provided with a first concave-convex structure with a corrugate shaped, the first concave-convex structure being abutted against the optical fiber; wherein a active space is formed between the sensing band and the inner watchband and configured for the radial artery to beat; a calibration assembly configured to continuously calibrate blood pressure values; and a signal process assembly.

In accordance with a method for characterization of particles in a fluid-filled hollow structure, an ultrasound signal with a frequency spectrum, which exhibits a local maximum at a variable measurement frequency, is emitted in the direction of a part area of the hollow structure and reflected components are detected. The measurement frequency is tuned in a predetermined measurement interval, and depending on the detected reflected components, a spectral response curve is acquired as a function of the measurement frequency. Depending on the response curve, at least one characteristic property for a part of the particles located in the part area of the hollow structure is determined. The characteristic property includes a measure for an adhesion of the particles of the part of the particles located in the part area of the hollow structure.