Dream stage enhancement uses a headband with EEG-EOG sensors, onboard processors, memory, coarse and fine time REM waveform detection modules, LEDs and an audio playback unit. After normalization to the user's EEG waveforms, the user's EEG-EOG signals are processed, REM and NREM stages detected and light, sound or AV stimuli are presented to the user based upon user-supplied light-sound-AV stimuli commands. To provide a reality check control (RCC), the head unit has a user actuatable RC interface whereby during sleep, RC stimuli are presented when the user depresses the RCC control which plays back the user supplied stimulus. In a learning mode, the user selects Recall or No Recall (NR) after the sleep period. If NR, then the system changes the color of light stimuli, light intensity, flash, audio sound type, audio intensity, and AV. If Recall the user supplied stimuli commands are carried out.

A method for controlling a scanner comprises: sensing an outer surface of a body of a subject to collect body surface data, using machine learning to predict a surface of an internal organ of the subject based on the body surface data, and controlling the scanner based on the predicted surface of the internal organ.

Human proximity detection techniques for wireless communication devices are described. In one embodiment, for example, an apparatus may comprise a memory and logic, at least a portion of the logic comprised in circuitry coupled to the memory, the logic to perform a connection establishment procedure to establish a wireless link with a human proximity reporting (HPR) device, identify heart rate information comprised in a human proximity report received from the HPR device via the wireless link, determine an initial HPR state based on the heart rate information, and select an initial operating mode for a feature of a human proximity monitoring (HPM) device based on the initial HPR state. Other embodiments are described and claimed.

An electronic device that can be worn on a user's body and an operating method thereof is disclosed. An electrode for charging and measuring is included in a front side of the electronic device. The electronic device includes a battery, a charging circuit for charging the battery, a bio-sensor, and a processor. The processor is configured to determine whether the battery is being charged through the charging circuit. If the battery is not being charged, the processor is configured to acquire biometric information by using a first method through the bio-sensor, and if the battery is being charged, the processor is configured to acquire the biometric information by using a second method through the bio-sensor.

Generally, methods, devices, and systems related to analyte monitoring and data logging are providede.g., as related to in vivo analyte monitoring devices and systems. In some aspects, methods, devices, and systems are provided that relate to enable related settings based on an expected use of an in vivo positioned sensor; logging or otherwise recording analyte levels acquired or derivede.g., sample analyte levels more frequently than they are logged or otherwise recorded in memory; dynamically adjust the data logging frequency; randomly determine times of acquiring or storing analyte levels from the in-vivo positioned analyte sensors; and enable recording related settings when the system is operable.

According to one embodiment, an information provision system including a biological sensor device including a sensor and an information transmitting terminal communicably connected to the biological sensor device is provided. The information transmitting terminal includes a detector. The detector detects an action of the user. The biological sensor device includes an obtaining module. The obtaining module obtains, when the action of the user is detected, biological data by driving the sensor during a measurement period included in a measurement information in association with the action.

A wearable electronic device (100) comprises a sensor (1) providing a sensor signal (s1), which sensor (1) is one of a temperature sensor and a humidity sensor. A control unit (3) determines, subject to at least the sensor signal (s1), if the wearable electronic device (100) is worn by a user, and provides an output signal (t1) indicative of a result of the determination.

A universal sensor pod provides a native sensing function during a first mode of operation and a secondary sensing function during a second mode of operation. The universal sensor pod may transition from the native sensing function to the secondary sensing function upon detecting that a sensor capable of the secondary sensing function is connected to the universal sensor pod via a smart connector. The universal sensor pod may continue one or more native sensing functions along with the secondary sensing function upon detecting that a sensor capable of the secondary sensing function is connected to the universal sensor pod via a smart connector. A code embedded within the smart connector is transmitted to a processor contained within the universal sensor pod and in response, the processor executes a firmware application that is tailored to the secondary sensing function code in response to receiving the code.

A device, system and method that communicate with at least one implantable medical device (IMD). The device includes a unit and a surface having at least one reception or transmission element that communicate with the at least one IMD. A minimum pressure required for the contact between transmission or reception elements and skin is provided by gravity or by patient interaction with the device. The system includes the at least one IMD, the unit that communicates with the at least one IMD and the device having the at least one reception or transmission element that communicate with the at least one IMD. The method includes the steps of providing a surface having at least one reception or transmission element that communicate with an IMD, and enabling communication upon detection of a minimum pressure on the surface. The communication with the IMD is acoustic or conductive.

Methods, devices, systems, and kits are provided that buffer the time spaced glucose signals in a memory, and when a request for real time glucose level information is detected, transmit the buffered glucose signals and real time monitored glucose level information to a remotely located device, process a subset of the received glucose signals to identify a predetermined number of consecutive glucose data points indicating an adverse condition such as an impending hypoglycemic condition, confirm the adverse condition based on comparison of the predetermined number of consecutive glucose data points to a stored glucose data profile associated with the adverse condition, where confirming the adverse condition includes generating a notification signal when the impending hypoglycemic condition is confirmed, and activate a radio frequency (RF) communication module to wirelessly transmit the generated notification signal to the remotely located device only when the notification signal is generated.