Systems and methods for tracking performance are provided. A method includes monitoring a first amplitude of a first muscle activity for a plurality of time. The method includes generating a plurality of measures of neuromuscular work for the plurality of time points using the first amplitude. The method includes determining a plurality of muscle activation quotients for the plurality of time points, using the plurality of measures of neuromuscular work. The method includes defining a plurality of muscle activation zones using the plurality of muscle activation quotients, wherein individual muscle activation zones correspond to ranges of values of the plurality of muscle activation quotients. The method includes generating a visualization of the plurality of muscle activation quotients and the plurality of muscle activation zones for the plurality of time-points. The method also includes outputting the visualization to a display.

One or more insertion mechanisms may be configured to insert and retract one or more needles associated with a component configured to implantable component into the tissue of a patient. For example, a component or implantable component may include a cannula for delivery of medication to a patient or an analyte sensor. An insertion mechanism may be configured to be part of or enclosed within a structure of the Disease Management System. For example, an insertion mechanism may be configured to operate within the structure of the Disease Management System and not require outside components or devices to apply one or more needles or implantable components to the patient.

One or more insertion mechanisms may be configured to insert and retract one or more needles associated with a component configured to implantable component into the tissue of a patient. For example, a component or implantable component may include a cannula for delivery of medication to a patient or an analyte sensor. An insertion mechanism may be configured to be part of or enclosed within a structure of the Disease Management System. For example, an insertion mechanism may be configured to operate within the structure of the Disease Management System and not require outside components or devices to apply one or more needles or implantable components to the patient.

A modular sensing assembly may be used to detect user inputs at an electronic device. Example user inputs include touch inputs, fingerprint inputs, translational inputs, audio inputs, biometric inputs, and the like. Inputs received using the modular sensing assembly may be used to control a graphical output of a display of the electronic device. A modular sensing assembly may be configured, for example, as a power button, a key of a keyboard, a control button (e.g., volume control), a home button, a watch crown, and so on.

A cardiac activity measurement assembly for a sports equipment handle and the handle is disclosed, wherein the assembly includes an optical cardiac activity sensor configured to measure cardiac activity of a user, and an attachment element for floatingly attaching the optical cardiac activity sensor to a handle of sports equipment in order to reduce pressure on a measuring head of the sensor caused by a skin contact between the measuring head and at least one finger or a palm of the user when gripping the handle.

An implantable vagus nerve stimulation (VNS) system includes a sensor configured to measure ECG data for a patient, a stimulation subsystem configured to deliver VNS to the patient, and a control system configured to perform a heart rate variability analysis with the ECG data. In some aspects, performing the heart rate variability analysis includes measuring R-R intervals between successive R-waves for the ECG data measured during a stimulation period and a baseline period, plotting each R-R interval against an immediately preceding R-R interval for each of the stimulation period and the baseline period, and determining at least one of a standard deviation from an axis of a line perpendicular to an identity line for each of the stimulation period plot and the baseline period plot or a centroid of each of the stimulation period plot and the baseline period plot.

An electronic device for identifying occurrence of hypotension and a method therefor are provided. The electronic device includes a housing, a user interface, a photoplethysmogram (PPG) sensor exposed through at least part of the housing, a motion sensor disposed in the housing, at least one processor operatively coupled with the user interface, the PPG sensor, and the motion sensor, and a memory operatively coupled with the at least one processor. The memory may store instructions which, when executed by the at least one processor, cause the at least one processor to, based on first data from the motion sensor indicating a change of a selected pattern, identify a blood pressure value based at least in part on second data from the PPG sensor, and based on the identified blood pressure value being lower than a first threshold, provide a notification through the user interface.

An apparatus for measuring blood pressure includes: a pulse wave measurer including a first light source configured to emit a first light, a second light source configured to emit a second light, and a photodetector configured to measure a pulse wave signal of an object based on the first light emitted by the first light source onto the object and returning from the object; a force measurer configured to measure a contact force between the object and the pulse wave measurer; and a processor configured to control emission of the second light from the second light source based on the measured contact force, and configured to estimate blood pressure of the object based on the measured pulse wave signal and the measured contact force.

Systems and methods are provided to combine multiple stimulation modalities to significantly increase the effectiveness of non-invasive stimulation. Multiple sensor and stimulation devices and modalities can be combined into a single, compact unit that minimizes the need for additional sensors or stimulation devices. The system features several subunits, referred to as sensory and stimulation devices (SSD), that are integrated into a headphone setup. The system is controlled by a centralized controller that communicates with all of the SSDs and with an external computer system that delivers learning material synchronized with the delivery of stimulations and the collection of user responses based on physiological signals.

Systems and methods are provided to combine multiple stimulation modalities to significantly increase the effectiveness of non-invasive stimulation. Multiple sensor and stimulation devices and modalities can be combined into a single, compact unit that minimizes the need for additional sensors or stimulation devices. The system features several subunits, referred to as sensory and stimulation devices (SSD), that are integrated into a headphone setup. The system is controlled by a centralized controller that communicates with all of the SSDs and with an external computer system that delivers learning material synchronized with the delivery of stimulations and the collection of user responses based on physiological signals.