A detection apparatus and a method are provided for detecting a respiratory movement of a patient. The detection apparatus includes at least two metallic U-shaped signal coupling elements that are interleaved so that between the signal coupling elements arises at least one coupling point at which a signal may be transferred between the two signal coupling elements. Analysis electronics are configured to detect a change in a receive signal produced in a second of the signal coupling elements that is acting as a receiver in the near-field region of the first signal coupling elements as a result of a signal given for one of the signal coupling elements that is acting as a transmitter being coupled into the second of the signal coupling elements, which change indicates the respiratory movement.

Disclosed herein are methods, systems, apparatuses, and media for sensing neuromuscular signals. In one example, a device for sensing neuromuscular signals comprises a wearable structure. The device includes a plurality of signal electrodes aligned along an interior portion of the wearable structure, each signal electrode configured to detect neuromuscular signals. The device further includes a plurality of amplifiers corresponding to the plurality of signal electrodes, wherein an amplifier has: a first input operatively coupled to a corresponding signal electrode; a second input; and an output corresponding to a neuromuscular signal channel. The device further includes circuitry configured to generate a common mode reference signal directly or indirectly based on signals from one or more electrodes, wherein the second input of each amplifier of the plurality of amplifiers is configured to receive the common mode reference signal or a signal based on the common mode reference signal.

Embodiments are directed to devices, systems and methods for determining a perspiration metric of a user. In some embodiments, a device may include a perspiration sensor having first and second electrodes positioned on a skin-facing exterior surface of the device. Capacitance circuitry may measure a capacitance between the electrodes, which may be used to calculate the perspiration metric. In some embodiments, the device defines a cavity such that one or both of the electrodes extend at least partially into the cavity. Other embodiments include a second perspiration sensor, and measurements from the second perspiration sensor may be used in calculating the perspiration metric.

Embodiments are directed to devices, systems and methods for determining a perspiration metric of a user. In some embodiments, a device may include a perspiration sensor having first and second electrodes positioned on a skin-facing exterior surface of the device. Capacitance circuitry may measure a capacitance between the electrodes, which may be used to calculate the perspiration metric. In some embodiments, the device defines a cavity such that one or both of the electrodes extend at least partially into the cavity. Other embodiments include a second perspiration sensor, and measurements from the second perspiration sensor may be used in calculating the perspiration metric.

A sensor device comprises at least two sensors at the end of a shaft (such as a guidewire or catheter). One sensor uses signals in a first frequency range and a first voltage range and the other sensor uses signals in a second frequency range different to the first frequency range and a second voltage range different to the first voltage range. The first sensor is shorted based on frequency analysis, thereby to prevent the first sensor being exposed to signals associated with the second sensor. This enables the two sensors to be driven by the same shared pair of wires along the shaft, with automatic selection of the suitable sensor.

A sensor device comprises at least two sensors at the end of a shaft (such as a guidewire or catheter). One sensor uses signals in a first frequency range and a first voltage range and the other sensor uses signals in a second frequency range different to the first frequency range and a second voltage range different to the first voltage range. The first sensor is shorted based on frequency analysis, thereby to prevent the first sensor being exposed to signals associated with the second sensor. This enables the two sensors to be driven by the same shared pair of wires along the shaft, with automatic selection of the suitable sensor.

An embodiment includes a bioelectrode including a hydrogel film, a conductive film, and a protective film. The conductive film is formed on one surface of the hydrogel film, and the protective film is formed on the other surface of the hydrogel film. The hydrogel film is comprises a mixture of a first material and a second material and is compatible with a living body, the first material configured to cause a sol-gel change at a temperature within a predetermined range around a body temperature of the living body and being compatible with the living body, the second material configured to not cause a sol-gel change at the temperature and being compatible with the living body. The protective film is provided to suppress the infiltration of water into the hydrogel film. The protective film can be made of a waterproof material or a water-repellent material.

An embodiment includes a bioelectrode including a hydrogel film, a conductive film, and a protective film. The conductive film is formed on one surface of the hydrogel film, and the protective film is formed on the other surface of the hydrogel film. The hydrogel film is comprises a mixture of a first material and a second material and is compatible with a living body, the first material configured to cause a sol-gel change at a temperature within a predetermined range around a body temperature of the living body and being compatible with the living body, the second material configured to not cause a sol-gel change at the temperature and being compatible with the living body. The protective film is provided to suppress the infiltration of water into the hydrogel film. The protective film can be made of a waterproof material or a water-repellent material.

An electrocardiogram measurement unit comprises: a pair of positive and negative electrode bodies and constituting capacitive coupling electrodes and arranged in a non-contact state with a human body; a signal amplification unit that amplifies an electric signal from both the electrode bodies and outputs the amplified electric signal as an electrocardiographic signal; and an inverting output unit that inverts an in-phase signal of the electric signal from both the electrode bodies and outputs an inverted signal. The electrocardiographic signal measurement device comprises simultaneously both channels and when the electrocardiogram measurement unit to which the inverted signal from the inverting output unit is input to the positive electrode body is defined as a first channel, and the electrocardiogram measurement unit to which the inverted signal from the inverting output unit is input to the negative electrode body is defined as a second channel.

An electrocardiogram measurement unit comprises: a pair of positive and negative electrode bodies and constituting capacitive coupling electrodes and arranged in a non-contact state with a human body; a signal amplification unit that amplifies an electric signal from both the electrode bodies and outputs the amplified electric signal as an electrocardiographic signal; and an inverting output unit that inverts an in-phase signal of the electric signal from both the electrode bodies and outputs an inverted signal. The electrocardiographic signal measurement device comprises simultaneously both channels and when the electrocardiogram measurement unit to which the inverted signal from the inverting output unit is input to the positive electrode body is defined as a first channel, and the electrocardiogram measurement unit to which the inverted signal from the inverting output unit is input to the negative electrode body is defined as a second channel.