The invention relates to a system for body-condition-dependent stimulation by means of function modules, e. g. an action module (2, D/A module) for stimulating tissue and a capture module (3, A/D module) for deriving/measuring bio data or bio signals, characterized in that the two modules communicate via a communication link (5) that meets hard or at least firm real-time requirements. The communication link (5) preferably comprises a real-time-capable bus to which the two modules are connected, above all an EtherCAT bus.

Applicators for applying an on-skin assembly to skin of a host and methods of their use and/or manufacture are provided. An applicator includes an insertion assembly configured to insert at least a portion of the on-skin assembly into the skin of the host, a housing configured to house the insertion assembly, the housing comprising an aperture through which the on-skin assembly can pass, an actuation member configured to, upon activation, cause the insertion assembly to insert at least the portion of the on-skin assembly into the skin of the host, and a sealing element configured to provide a sterile barrier and a vapor barrier between an internal environment of the housing and an external environment of the housing.

The present invention relates to a sensor applicator assembly for a continuous glucose monitoring system and provides a sensor applicator assembly for a continuous glucose monitoring system, which is manufactured with a sensor module assembled inside an applicator, thereby minimizing additional work by a user for attaching the sensor module to the body and allowing the sensor module to be attached to the body simply by operating the applicator, and thus can be used more conveniently. A battery is built in the sensor module and a separate transmitter is connected to the sensor module so as to receive power supply from the sensor module and be continuously used semi-permanently, thereby making the assembly economical. The sensor module and the applicator are used as disposables, thereby allowing accurate and safe use and convenient maintenance.

A quantitative gait training and/or analysis system includes one or more footwear modules that may include a piezoresistive sensor, an inertial sensor and an independent logic unit. The footwear module functions to permit the extraction of gait kinematics and evaluation thereof in real time, or data may be stored for later reduction and analysis. Embodiments relating to calibration-based estimation of kinematic gait parameters are described.

A person support apparatus, such as a bed, stretcher, cot, recliner, or the like, includes an exit detection system having a plurality of force sensors that support the weight of an occupant positioned on a support surface and obstruction detection system having one or more obstruction sensors. The force sensors are part of an exit detection system that issues an alarm when the occupant exits, or is about to exit, the person support apparatus. The bed exit system can react to detection of an obstacle. The distribution of weight applied to the force sensors is used to determine if the occupant is about to exit the person support apparatus. Compensation is made to the exit detection system for changes in the weight distribution that are not caused by movement of the occupant. Such changes may be due to not only movement of the person support apparatus or components thereof, but obstacles encountered by the person support apparatus or components thereof.

A monitoring system includes a first acquisition unit that acquires identification information unique to a user, a second acquisition unit that acquires position information of the user, an action history calculation unit that obtains an action history of the user from the identification information of the user acquired by the first acquisition unit and the position information acquired by the second acquisition unit, and a presentation unit that presents the action history of the user calculated by the action history calculation unit, wherein the action history includes at least one of a period for which and a frequency at which the user stayed at a position indicated by the position information.

Systems and methods for prompting a user to perform an exercise and monitoring the exercise are provided. Multiple independent sensors or sensor systems may be used to calculate energy expenditure. Various criteria may be used to manually or automatically select the independent sensor or sensor system or combination that will be used with the energy expenditure calculations.

The present disclosure relates in general to a device and a method for providing a measure of a circumference of a body part. More specifically, the present disclosure relates to how to provide a measure of a circumference of a body part, wherein the body part may have swelled, such that it for example can be observed whether the body part swells further or less. Most specifically, the swelled body part may be swelled due to oedema and/or lymphoedema.

A biological information measuring apparatus includes a detector, a measuring unit, a calculator, and a determining unit. The detector detects pulse waves continuously. The measuring unit measures first biological information. The calculator calculates second biological information from the pulse waves based on the first biological information. The measuring unit suspends the measurement and resumes the measurement after a lapse of a period in a case where the determining unit does not determine that the result of measurement is normal, and the measuring unit continues the measurement in other cases where the body motion is not generated, the pulse waves are not irregular or the blood pressure value fails to vary.

Systems include an invasive sensor and a non-invasive sensor for detection of analytes. The invasive sensor detects one or more non-invasively detected analytes, and the non-invasive sensor detects one or more invasively detected analytes. The one or more non-invasively detected analytes and the one or more invasively detected analytes can include at least one analyte in common, or do not include any analytes in common. The detection of the one or more non-invasively detected analytes and the detection of the one or more invasively detected analytes can be used to