The circuit may include bio-stimulating signal generating circuit which generates a bio-stimulating signal in a bio-stimulating mode, a bio-signal electrode which delivers the bio-stimulating signal generated in the bio-stimulating mode and receives a bio-signal in a bio-signal measuring mode, a switch block which is turned on when a voltage of the bio-stimulating signal is greater than a first reference voltage which is greater than a second reference voltage or lower than the second reference voltage, first and second resistors, and a bio-signal measuring circuit which measures voltage signals divided by the first and second resistors or measures a signal of the bio-signal electrode according to whether the switch block is turned on. The first and second resistors may be serially connected between the bio-signal electrode and the switch block, and divide a voltage of a signal of the bio-signal electrode when the switch block is turned on.

A smart phone includes photoelectric pulse wave sensing units that obtain photoelectric pulse wave signals from hands holding the smart phone, a touch screen on which a plurality of operation switches that accept operations performed by thumbs are displayed, and a switch arrangement changing unit that changes the arrangement of the displayed plurality of operation switches. The switch arrangement changing unit, when photoelectric pulse wave signals are obtained by the photoelectric pulse wave sensing units, changes the arrangement of the operation switches displayed on the touch screen in such a manner that the operation switches are arranged along a circular arc of a virtual circle whose center is located at a carpometacarpal joint of the thumb of a right hand performing operations and whose radius is the distance from the carpometacarpal joint to the tip of the thumb.

A medical device provides stimulation therapy to a patient based on a set of therapy parameters. One or more therapy parameters may be automatically adjusted based on acceleration forces detected by a sensor, the acceleration forces being applied to the patient. In some examples, adjustments to one or more therapy parameter may be made based on an algorithm. The algorithm may be defined by acceleration and therapy parameter value pairs associated with opposite patient positions.

Described herein are apparatuses (e.g., garments, including but not limited to shirts, pants, and the like) for detecting and monitoring physiological parameters, such as respiration, cardiac parameters, and the like. Also described herein are methods of forming garments having one or more stretchable conductive ink patterns and methods of making garments having one or more highly stretchable conductive ink pattern formed of a composite of an insulative adhesive, a conductive ink, and an intermediate gradient zone between the adhesive and conductive ink. The conductive ink typically includes between about 40-60% conductive particles, between about 30-50% binder; between about 3-7% solvent; and between about 3-7% thickener. The stretchable conductive ink patterns may be stretched more than twice their length without breaking or rupturing.

An electrode lead may comprise a flexible circuit that includes a planar dielectric substrate including an elongated lead substrate portion having opposing ends, an electrode carrying substrate portion disposed on one end of the lead substrate portion, and a connector substrate portion disposed on the other end of the lead substrate portion, wherein the lead substrate portion is pre-shaped into a three-dimensional structure. The flexible circuit may further include an electrically conductive trace extending from the connector substrate portion to the electrode carrying substrate portion, a first window formed in the connector substrate portion to expose the electrically conductive trace to form a connector pad, and a second window formed in the electrode carrying substrate portion to expose the electrically conductive trace to form an electrode pad. The electrode lead may further comprise a lead connector that incorporates the connector substrate portion.

Wearable electronic devices that employ techniques for routing signals between components are described. An exemplary wearable electronic device includes a set of pod structures with each pod structure positioned adjacent and physically coupled to at least one other pod structure. The set of pod structures includes multiple sensor pods and at least one processor pod. Each sensor pod includes an on-board sensor to in use detect user-effected inputs and provide signals in response to the user-effected inputs. The signals are serially routed via successive ones of adjacent pod structures by respective communicative pathways until the signals are routed from the sensor pods to the processor pod. A processor on-board the processor pod processes the signals. Systems, articles, and methods for routing electrical signals and/or optical signals, including analog signals and/or digital signals, between pod structures are described.

Wearable electronic devices that employ techniques for routing signals between components are described. An exemplary wearable electronic device includes a set of pod structures with each pod structure positioned adjacent and physically coupled to at least one other pod structure. The set of pod structures includes multiple sensor pods and at least one processor pod. Each sensor pod includes an on-board sensor to in use detect user-effected inputs and provide signals in response to the user-effected inputs. The signals are serially routed via successive ones of adjacent pod structures by respective communicative pathways until the signals are routed from the sensor pods to the processor pod. A processor on-board the processor pod processes the signals. Systems, articles, and methods for routing electrical signals and/or optical signals, including analog signals and/or digital signals, between pod structures are described.

Methods, systems, and devices for assessing breathing disorders such as apneas and hypopneas are provided. An airflow monitoring device can be positioned in thermal communication with respiratory airflow (nasal and/or oral airflow). The airflow monitoring device can include a thermistor configured to measure heating and cooling cycles of respiratory airflow and determine respiratory airflow velocity from analysis of thermistor cooling. This velocity, alone or in combination with other physiological parameters, such as blood oxygen saturation, respiration effort, heart rate, body movement, etc. can be employed to assess sleep disorders.

Methods, systems, and devices for assessing breathing disorders such as apneas and hypopneas are provided. An airflow monitoring device can be positioned in thermal communication with respiratory airflow (nasal and/or oral airflow). The airflow monitoring device can include a thermistor configured to measure heating and cooling cycles of respiratory airflow and determine respiratory airflow velocity from analysis of thermistor cooling. This velocity, alone or in combination with other physiological parameters, such as blood oxygen saturation, respiration effort, heart rate, body movement, etc. can be employed to assess sleep disorders.

The present application relates to the field of wearable devices and provides a dominant limb identification method and device. The method may comprise acquiring first somatosensory information of a first limb of a user and determining whether the first limb is a dominant limb according to the first somatosensory information and reference information. The method and device enable a device worn by the user to perform automatic setting according to the identification result, thereby improving user experience.