The invention refers to a system for delivering a machine-learning based behavioral intervention for the care of withdraw symptoms such as Neonatal Abstinence Syndrome in neonates. The system obtains biosensor or behavioral information about a patient from a wearable device on the patient and makes a determinative recommendation or takes appropriate action based on its evaluation. The biosensor and behavioral information is collected by way of a wearable device over progressive periods of time. When the data is indicative of a need for treatment because the patient is exhibiting symptoms or indicating relapse traits, this information is sent to the system for evaluation. When the data is indicative of a need for treatment, action is taken in the form of a recommendation or when the device is configured to support direct treatment, direct action can be taken to modify alleviate the patient.

The invention refers to a system for delivering a machine-learning based behavioral intervention for the care of withdraw symptoms such as Neonatal Abstinence Syndrome in neonates. The system obtains biosensor or behavioral information about a patient from a wearable device on the patient and makes a determinative recommendation or takes appropriate action based on its evaluation. The biosensor and behavioral information is collected by way of a wearable device over progressive periods of time. When the data is indicative of a need for treatment because the patient is exhibiting symptoms or indicating relapse traits, this information is sent to the system for evaluation. When the data is indicative of a need for treatment, action is taken in the form of a recommendation or when the device is configured to support direct treatment, direct action can be taken to modify alleviate the patient.

The present invention relates to a stimulation electrode comprising an ionically conductive pressure sensitive adhesive composition comprising a) a (meth)acrylate resin comprising at least 10% of a (meth)acrylate monomer comprising OH-group by weight of the total weight of the (meth)acrylate resin; and b) an ionic liquid. The stimulation electrode according to the present invention is used in skin applications transferring an electrical signal to the body via skin.

The present invention relates to a stimulation electrode comprising an ionically conductive pressure sensitive adhesive composition comprising a) a (meth)acrylate resin comprising at least 10% of a (meth)acrylate monomer comprising OH-group by weight of the total weight of the (meth)acrylate resin; and b) an ionic liquid. The stimulation electrode according to the present invention is used in skin applications transferring an electrical signal to the body via skin.

A composite wiring includes: elastic wiring comprising an elastic tube, a conductor wire disposed inside the tube, and fixing portions that fix the conductor wire and the tube together at both ends of the tube in the lengthwise direction thereof, the length of the conductor wire between the fixing portions when the tube is in an unextended state being longer than the length of the tube between the fixing portions; other wiring separate from the elastic wiring; and a connection member that connects the conductor wire of the elastic wiring and a conductor wire of the other wiring by caulking in a state of being brought into contact with each other, the connection member having an interior section sealed in a watertight manner with a sealing material.

A method includes receiving acoustic inputs; generating signal channels from the acoustic inputs; pre-processing data in the signal channels; extracting S1-S2 peaks from the pre-processed data; removing artifacts and outliers from the S1-S2 peaks; generating S1-S2 signal channels based on the S1-S2 peaks in the pre-processed signal channels; selecting two or more of the S1-S2 signal channels; and combining the selected two or more S1-S2 signal channels to produce an acoustic uterine monitoring signal.

Provided is a bio-signal detection and stimulation device. The bio-signal detection and stimulation device includes a flexible substrate, a stimulation part on the flexible substrate, and a detection electrode part on the flexible substrate. The stimulation part and the detection electrode part vertically overlap each other, the stimulation part includes an organic light emitting diode (OLED), the stimulation part emits an optical signal, and the detection electrode part detects a bio-signal.

Provided is a bio-signal detection and stimulation device. The bio-signal detection and stimulation device includes a flexible substrate, a stimulation part on the flexible substrate, and a detection electrode part on the flexible substrate. The stimulation part and the detection electrode part vertically overlap each other, the stimulation part includes an organic light emitting diode (OLED), the stimulation part emits an optical signal, and the detection electrode part detects a bio-signal.

The present application relates to an electrophysiologically based Spectro-Temporal Modulation (STM) test unit. The STM test unit comprises an STM stimulus generating unit, an output unit, wherein the STM stimulus generating unit is configured to provide STM test stimuli comprising at least one STM probe stimulus to a user via the output unit according to a predetermined STM test protocol. The STM test unit further comprises one or more electrodes for measuring electrophysiological responses of the user, and an analysis unit configured to analyse the recorded electrophysiological responses of the user measured in response to the provided stimuli. The present application further relates to a method of electrophysiologically based STM testing of a user.

The present application relates to an electrophysiologically based Spectro-Temporal Modulation (STM) test unit. The STM test unit comprises an STM stimulus generating unit, an output unit, wherein the STM stimulus generating unit is configured to provide STM test stimuli comprising at least one STM probe stimulus to a user via the output unit according to a predetermined STM test protocol. The STM test unit further comprises one or more electrodes for measuring electrophysiological responses of the user, and an analysis unit configured to analyse the recorded electrophysiological responses of the user measured in response to the provided stimuli. The present application further relates to a method of electrophysiologically based STM testing of a user.