A wearable device configured to measure one or more physiological parameters of a user is described. In some embodiments, the wearable device includes: a top frame, a bottom frame connected to the top frame, and an interior between the top and bottom frames; a circuit board positioned within the interior; a first temperature sensor coupled to the circuit board and configured to generate one or more signals responsive to thermal energy of the user; and a second temperature sensor coupled to the circuit board and configured to generate one or more signals responsive to at least one of temperature within said interior and temperature outside said interior. In some embodiments, the circuit board is positioned between the first and second temperature sensors and no air gap is present between either of the first and second temperatures and the circuit board.

An embodiment of the present disclosure seeks to select characteristics of incoming intensity data that cause comparisons of selected characteristics to produce defined probe off space having reduced crossover with defined probe on space. Once defined, the present disclosure compares characteristics of incoming intensity data with the now defined probe off space, and in some embodiments, defined probe on space, to determine whether a probe off condition exists. When a processor determines a probe off condition exists, the processor may output or trigger an output signal that audibly and/or visually indicates to a user that the optical sensor should be adjusted for a proper application to a measurement site.

The present disclosure generally relates to a physiological device (100) for an animal The physiological device (100) comprises: a housing (120) comprising a channel (122) therethrough; an attachment layer (140) disposed on the housing (120) for attaching the physiological device (100) to an integument portion (50) of the animal; and a sensor unit (160) comprising a set of physiological sensors (162) for measuring physiological signals from the animal integument portion (50), the sensor unit (160) engageable with the channel (122) for axial displacement within the channel (122), wherein when the device (100) is attached to the animal integument portion (50), the sensor unit (160) is axially displaceable within the channel (122) for adjusting contact with the animal integument portion (50) for measuring the physiological signals.

Devices, systems and methods are disclosed that allow a patient to self-treat a medical condition, such as migraine headache, by electrical noninvasive stimulation of a vagus nerve. The system comprises a stimulator that is applied to the surface of the patient's neck. The device housing transmits data to a patient interface device such as a mobile phone or computer relating to the status of a stimulation session. The interface device in turn may communicate with a database contained within other computers, via a network or the internet. The system is designed to address problems that arise particularly during self-treatment, when a medical professional is not present.

At least one of at least one data-dependent scale factor or at least one data-dependent detection threshold is determined responsive to at least one block of time-series data of an auscultatory-sound signal generated by an auscultatory-sound sensor operatively coupled to a portion of the skin of a test-subject, wherein the at least one data-dependent scale factor or at least one data-dependent detection threshold provides a measure of a range of values of the at least one block of time-series data in relation to a predetermined metric, and is used to determine whether or not the auscultatory-sound sensor is either debonded or detached from the skin of the test-subject.

A control system controls an endoscope probe in manual mode or robot mode. The system comprises a handle attached to the probe; a portable display controller connectable to the handle; a robotic controller in communication with the handle and/or the portable display controller; and a support platform to which the probe and the portable device controller are attachable according to control mode. In manual mode, the handle is detached from the platform and connected to the portable display controller such that the probe is manually navigated to a first position inside a lumen. In robot mode, the handle is attached to the platform such that the robotic controller cooperates with the handle to robotically navigate the probe to a second position inside the lumen. The portable display controller includes a control section for manipulating the probe and a display section for displaying images of the lumen acquired in both modes.

A motion analytics system has a therapy boot, a camera for capturing motion of the therapy boot, and an external computing device communicatively coupled to the camera and the therapy boot. The therapy boot includes a foot portion, a shank portion, and a sole portion. The shank portion is disposed adjacently above the foot portion. The sole portion is disposed under the foot portion and includes sensors configured to detect motion of a user's foot. The external computing device receives motion data from the sensors and performs a data analytics method. The method includes organizing the received data; filtering at least a portion of the organized data through a frequency-based signal processing filter to remove background noise and interference therefrom; determining analytical data associated with one or more foot factors based on the filtered data; and categorizing the determined analytical data to provide context and insight about the user's motion.

A patient-monitoring device includes an adapter with a flexible printed circuit, the flexible printed circuit includes a rigid portion with a rigid stiffener and a flexible portion with a trace, and with a connector that is connected to one end of the trace, that is movable in two or three dimensions independent of the rigid portion, and that is connectible to an electrode assembly.

Disclosed herein is a waste detection system. The waste detection system includes a pad configured to acquire a fluid sample excreted from a patient. The pad includes one or more layers and at least one microfluidic channel configured to receive therein the fluid sample. The waste detection system further includes an intake manifold in fluid communication with the at least one microfluidic channel, the intake manifold configured to receive the fluid sample, the intake manifold having one or more reagents configured to detect the presence of waste within the fluid sample excreted from the patient.

A patch for a therapeutic electrical stimulation device includes a shoe connected to the first side of the patch, the shoe including a body extending in a longitudinal direction from a first end to a second end, and having first and second surfaces, the first end of the shoe defining at least two ports, and the first surface of the shoe defining a connection member. The patch also includes at least one conductor positioned in the ports of the first end of the shoe. The shoe is configured for sliding insertion into a receptacle defined by a controller so that the conductor is connected to the controller to deliver electrical current from the controller, through the conductor, and to the electrodes, and the connection member is at least partially captured by a detent defined by the controller in the receptacle to retain the shoe within the receptacle.