Abstract: Present invention provide a system and a method for recording, evaluating, screening and monitoring life style associated Non-communicable diseases related data of a subject via an Integrated Medical Device (IMD) in real time, and sharing the same on a server, either local or cloud based, for fast, active sharing of data by remote users anytime anywhere.

Abstract: A guidewire system includes an elongated wire configured for insertion into a luminal space, such as the vasculature, of a body. The wire is conductive and configured to conduct electrical signals. One or more sensors are coupled to a distal section of the wire and configured to send and receive the electrical signals via the wire. The wire through which the one or more sensors are coupled is the only wire through which the one or more sensors send and receive the electrical signals.

Abstract: Disclosed is a physiologic monitoring system comprising a central hub in communication with a management portal for communicating physiologic measurements taken from a plurality of peripheral devices on a patient. At least one non-invasive peripheral device may measure physiologic data from a patient and be in communication with said central hub. A system including an invasive peripheral device may be associated with said patient and be in communication with said central hub. The central hub may be scalable to collect and communicate measurements from the non-invasive peripheral device and the invasive peripheral device. The at least one non-invasive peripheral device may include a blood pressure cuff, an oxygen sensor, a weight scale, and an ECG monitor. The invasive peripheral device may include a wireless sensor reader that may be adapted to measure physiologic data from a sensor implant placed within the cardiovascular system of said patient.

Abstract: Disclosed are system, method, and computer program product embodiments for determining a digital marker. An embodiment operates by determining one or more oculometric parameters associated with an eye of a user using a video stream. The video stream comprises at least one image of a face of the user. The embodiment then determines a pupillary response function of brightness or a gaze response function by performing a deconvolution process based on at least the one or more oculometric parameters. The pupillary response function of brightness or the gaze response function is indicative of a response of the eye of the user to an external factor. The embodiment determines one or more digital markers of the user based on the pupillary response function of brightness or the gaze response function. The one or more digital markers are indicative of a neurological condition or a mental health condition of the user.

Abstract: The present invention relates to a customized stretchable wearable device and a manufacturing method therefor, enabling the manufacturing of a customized stretchable wearable device which fits the body characteristics of a wearing subject who is wearing the wearable device, thereby enabling good wear comfort and sense of operation, and also a beautiful exterior.

Abstract: Implementations relate to role change requests that can be delayed and/or implemented according to circumstances associated with an interaction between a user and an automated assistant. A role change request can cause a designation of auxiliary devices (e.g., earbuds and/or any other peripheral devices) to be changed, and at least cause a different auxiliary device to be tasked with directly communicating with a principal device (e.g., a cellular phone). For instance, when an auxiliary device is requesting a role change request during an assistant interaction, an operating system of the principal device can identify factors that form the basis for determining whether to immediately implement the role change request or, instead, to delay or refuse implementation of the role change request. When the factors indicate that the role change request is not particularly urgent, the operating system can cause the role change request to be delayed until the assistant interaction is complete.

Abstract: An intraoral device wearable by a patient may include an intraoral device body, a first advancement structure configured to be coupled to a first jaw of the patient. and a second advancement structure configured to be coupled to a second jaw of the patient. The device may also include an intraoral actuator coupled to the first advancement structure to displace a lower jaw of the patient from a first position to a second position. The first position may be a habitual jaw position and the second position may be a modified jaw position. Displacing the lower jaw of the patient may include moving the lower jaw from the habitual jaw position to the modified jaw position based at least in part on data from at least one sensor.

Abstract: Provided is a system capable of determining a stress coping style of a test subject in a non-contact state. The system includes a biological information acquiring part which acquires biological information of a test subject in a non-contact state, and a determining part which determines a stress coping style of the test subject based on the biological information and a response pattern specified in advance. The response pattern is specified by a hemodynamic parameter.

Abstract: An autonomous working system includes an autonomous working apparatus and a second apparatus independent of the autonomous working apparatus. The autonomous working system includes a control circuit, wherein the control circuit includes a rain sensor, including a first electrode and a second electrode; a switching circuit, connected to the first electrode and the second electrode, and configured to operatively exchange the polarities of the first electrode and the second electrode; a detection module, configured to obtain an electrical signal of the rain sensor; a judgement module, configured to determine whether the electrical signal and a first threshold satisfy a first relationship; and a behavior control module, configured to control the autonomous working apparatus to change the behavior status when it is determined that the electrical signal and the first threshold satisfy the first relationship.

Abstract: A system and method for creating small data size representations of images, created on the image detection device, over wireless connections when there is insufficient bandwidth to support detailed images is disclosed. Image data size is often too large to send over low-powered long-distance wireless connections. Image data must be dramatically reduced to enable use of the lowest-power longest-distance wireless platforms including LoRa with LoRaWAN. Common image compression algorithms include jpeg and mpeg that provide only moderate reductions in data size. The described invention reduces data size beyond jpeg compression by reducing targeted image objects to simple outlines, contours or vectors. Monitoring security, wildlife, agricultural and other natural events require images of objects including insects, crops, livestock, wildlife or intruders. Contours, outlines or vectors of targeted objects are often sufficiently recognizable to provide useful information.

Abstract: System and methods are provided for augmented reality displays for medical and physiological monitoring. Augmented reality user interfaces are virtually pinned to a physical device, a location, or to a patient. An augmented reality position determination process determines the presentation of user interfaces relative to reference positions and reference objects. Detection of gestures causes the augmented reality users interfaces to be updated, such as pinning a user interface to a device, location, or patient. Looking away from an augmented reality user interface causes the user interface to minimize or disappear in an augmented reality display. An augmented reality gesture detection process determines gestures based on captured image data and computer vision techniques performed on the image data.

Abstract: This disclosure is related to methods of objectively detecting and measuring neuropathic pain in a subject.

Abstract: A method includes obtaining prescribing drug information and published guidelines for each of a plurality of ADMs available for managing glucose levels, and receiving patient information associated with a patient. The method also includes ordering total demerit values from lowest to highest, selecting a predetermined number of recommended ADMs associated with the lowest total demerit values, and determining a recommended dosage for each recommended ADM. The method also includes transmitting a therapy regimen to a patient device associated with the patient. The therapy regimen includes the recommended ADMs and the recommended dosage for each recommended ADM.

Abstract: A first collection of biometric data of a user on a mattress of the bed system is sensed via a sensor of the bed system. The user is instructed to perform an exercise activity. The user is instructed to return to and lay on the mattress after performing the exercise activity. A second collection of biometric data of the user on the mattress of the bed system is sensed via the sensor of the bed system again after the user has performed the exercise activity. A stress test output is generated based on the sensed first biometric data and the sensed second biometric data. The stress test output is displayed to the user.

Abstract: Embodiments disclosed herein utilize biometric verification from wearable devices to approve access for shared spaces. Requests to occupy the shared spaces are received and conditional reservations are made pending health checks of the requesters. Prior to occupation, fresh biometric measurements are captured via the user's wearable device, which include physiological signals validating both ongoing good health as well as identity match to the original requester. When recent biometric verification indicates both healthy status and unchanged identity, access to the reserved space is approved. These embodiments securely manage reservations while protecting the health of other occupants through conditional access related to the requester's current health condition.

Abstract: The present disclosure generally relates to user interfaces for health applications. In some embodiments, exemplary user interfaces for managing health and safety features on an electronic device are described. In some embodiments, exemplary user interfaces for managing the setup of a health feature on an electronic device are described. In some embodiments, exemplary user interfaces for managing background health measurements on an electronic device are described. In some embodiments, exemplary user interfaces for managing a biometric measurement taken using an electronic device are described. In some embodiments, exemplary user interfaces for providing results for captured health information on an electronic device are described. In some embodiments, exemplary user interfaces for managing background health measurements on an electronic device are described.

Abstract: An apparatus for estimating a core body temperature of an object is provided. According to one embodiment, the apparatus includes a plurality of sensors configured to obtain data from an object and a processor configured to obtain a surface temperature, a heat flux, a skin blood flow rate, and a blood flow velocity by using the data obtained from the plurality of sensors, obtain a skin thermal conductivity based on the skin blood flow rate, and estimate a core body temperature of the object based on the surface temperature, the heat flux, the skin thermal conductivity, and the blood flow velocity of the object.

Abstract: In part, the invention relates to methods, apparatus, and systems suitable for determining a fractional flow reserve (FFR) and variations of modifications thereof One embodiment relates to a method and apparatus for obtaining a corrected FFR in a vessel having a stenosis. In one aspect, the invention relates to an apparatus for measuring corrected FFR of a vessel having a stenosis. In one embodiment, the apparatus includes a probe comprising an optical coherence tomography assembly and a pressure assembly; and a processor in communication with the optical coherence tomography assembly and the pressure assembly. In one embodiment, the pressure assembly measures values of pressure in predetermined locations the vessel and communicates them to the processor. In one embodiment, a dual guidewire is used to reduce the interference in the pressure measurement.

Abstract: An illumination system for eye tracking is described herein. The illumination system may include a laser light source and an ultra-fast scanning micro-electromechanical system (MEMS) operating at a frequency range from about 10 kHz to about 100 kHz to reflect laser light to the eye and generating a desired fringe pattern controlling intensity and timing. A surface of the MEMS may include diffractive optical element (DOE) to reflect the laser light as a concentrated optical beam. The light may also be projected by grating-based illuminators on a photonic integrated circuit (PIC) controlled through adiabatic couplers projecting multiple binary/grayscale images onto the eye. On the detection side, a 2D single-photon avalanche diode (SPAD) sensor or a SPAD array detector and an active MEMS shutter array may be used. Compressive sensing techniques may be applied on the detection side.

Abstract: Techniques for prioritizing similarities and differences during responses to incidents based on incident context are provided. Video and audio of an initial response to a first incident at an incident location is monitored. A context for the initial response is created. Video and audio of a subsequent response to a second incident at the incident location is monitored. The video and audio of the initial response and the subsequent response is compared. A machine learning model prioritizes the similarities and differences between the video and audio based on the context. The similarities and differences between the video and audio are provided to a subsequent responder based on the prioritization.

Abstract: A system and method of displaying neonatal health information are disclosed. In one aspect, the method includes receiving data characterizing a start of an APGAR timer; receiving a time value associated with a current time of the APGAR timer; receiving and displaying on an electronic display a plurality of time windows and a corresponding plurality of target values, each of the plurality of target values representing a predetermined blood oxygen threshold value in connection with a corresponding one of the plurality of time windows; receiving and displaying on an electronic display a measured blood oxygen level value; and highlighting, on the electronic display, a first of the plurality of target values and a corresponding first of the plurality of time windows when the time value associated with the current time of the APGAR timer reaches a first time value.

Abstract: A method to measure sound-producing behaviors of a subject with a power- and bandwidth-limited electronic device that includes a processor includes measuring, by a microphone communicatively coupled to the processor, sound in a vicinity of the subject to generate an audio data signal that represents the sound. The method also includes measuring, by at least one second sensor communicatively coupled to the processor, at least one parameter other than sound to generate at least a second data signal that represents the at least one parameter other than sound. The method also includes detecting one or more sound-producing behaviors of the subject based on: both the audio data signal and the second data signal; or information derived from both the audio data signal and the second data signal.

Abstract: Wearable sensors and uses thereof are disclosed. Preferred sensors include surface EMG electrodes for measuring electrical muscle activity, by which muscle contraction is measured. Such muscle contraction can be used to determine a person's posture, especially when the contraction being measured is that of core muscles. An alert preferably is provided to a person in real time when an incorrect posture is detected. By providing such biofeedback, a person is trained in maintaining a good posture. Such posture training is believed to heal alleviate or even present lower back pain. Wearable sensors of the invention also can be used to measure contraction in muscles during exercise, including running and strength training, to gain information for use in improving such activities.

Abstract: Methods and systems are provided for measuring anatomical dimensions from a single two-dimensional (2D) digital image. The digital image is taken from the front/anterior view using a mobile, handheld communication device. The linear measurements are used to estimate the body volume of the individual. Total body density is calculated from estimated body volume and body weight. Body composition (fat mass and fat-free mass) of the individual is derived from density using known mathematical conversion formulas. A method for estimating body composition analysis is provided. Systems and methods are provided that determine an individual's fitness by determining body composition of the individual using a picture of the individual, determining the individual's VO2 max based on the individual's movement (e.g., walking and/or running a measured distance over a measured amount of time), and determining the individual's fitness based on the body composition and the determined VO2 max.

Abstract: A method for monitoring intoxication of a user, the method including: receiving a set of samples from a body region of a user; generating an intoxication metric based on the set of samples; and providing a notification to the user based on the intoxication metric. The method can additionally or alternatively include: modifying operation of the transdermal alcohol sensing device based on the intoxication metric; determining contextual data; maintaining a hydration level of the transdermal alcohol sensing device; and any other suitable processes. A system for monitoring intoxication of a user including a sensor and a housing. The system can additionally or alternatively include any or all of: an inlet, a fastener, an electronics subsystem, a user device, and/or any other suitable component.

Abstract: A system and a method of performing screening tests for diagnosing a developmental condition of a human subject may include: receiving one or more profile data elements pertaining to the human subject; receiving one or more first behavioral data elements that may include information that is indicative of a behavior of a human subject from one or more data sources; analyzing the one or more first behavioral data elements in view of the one or more profile data elements to obtain a suspected impediment of development of the human subject; and presenting to the human subject a personalized test, adapted to diagnose the developmental condition of the human subject in view of the suspected impediment, to perform on a UI of a computing device according to the suspected impediment.

Abstract: Wireless systems and methods are provided for protecting vital organs from blood flow loss, and for physiological monitoring of a subject in various settings. The systems and methods permit the coordinated delivery of various treatment protocols involving inflation or deflation of cuffs to multiple limbs of the subject.

Abstract: A device for implantation in a left atrial appendage of the heart comprises docking station comprising a radially expansible element that is adjustable between a contracted orientation suitable for transluminal delivery and a deployed orientation configured to anchor within the left atrial appendage and fluidically isolate the left atrial appendage from the left atrium, the docking station also includes a recessed socket accessible from the left atrium through an opening, and a closure coving the opening. A modular active element is configured for detachable engagement within the recessed socket of the docking station. The modular active element comprises a treatment element configured to electrically stimulate heart tissue, thermally stimulate heart tissue, electroporate heart tissue, or deliver a substance into heart tissue or a chamber of the heart, or a sensing element configured to detect a parameter selected from temperature, pressure, electrical signal, heart rate, or respiratory rate.

Abstract: Disclosed are devices, systems and methods for implantable a biofuel cells. In some aspects, a biofuel cell device for extracting energy from a biological fluid includes a substrate including two compartments each with one or more openings; an anode assembly disposed in the substrate and including an anode electrode and functionalization material to facilitate an oxidative process that releases electrons captured at the anode electrode; and a cathode assembly disposed in the substrate separated from the anode assembly and including a catalytic material facilitate a chemical reduction process such that the biofuel cell device extracts electrical energy from the substance in the biological fluid.

Abstract: A method of monitoring hydration including obtaining biological data for a given period of time, wherein the biological data includes measurements of one or more biological indicators; converting the biological data into a baseline value; obtaining real-time biological data from one or more biological sensors; performing a pre-processing analysis of the real-time biological data; comparing the real-time biological data with baseline value to create a hydration index.

Abstract: An apparatus for estimating a core body temperature of an object is provided. According to one embodiment, the apparatus includes a plurality of sensors configured to obtain data from an object and a processor configured to obtain a surface temperature, a heat flux, a skin blood flow rate, and a blood flow velocity by using the data obtained from the plurality of sensors, obtain a skin thermal conductivity based on the skin blood flow rate, and estimate a core body temperature of the object based on the surface temperature, the heat flux, the skin thermal conductivity, and the blood flow velocity of the object.

Abstract: A technology for obtaining a respiratory rate from a photoplethysmogram (PPG) signal. In one example, an artificial neural network model can be trained to predict a respiratory rate using a training dataset containing PPG data. The artificial neural network model can include a first series of convolutional layers to remove artifacts from a PPG signal, a fast Fourier transform (FFT) layer to convert the PPG signal to PPG frequency representations, and a dense layer to decode the PPG frequency representations to respiratory rate predictions. After training the artificial neural network model, PPG data generated by a pulse oximeter monitor can be obtained, and the PPG data can be input to the artificial neural network model. The artificial neural network model outputs a respiratory rate prediction, wherein the respiratory rate prediction represents the respiratory rate obtained from the PPG signal.

Abstract: In a sensor system (12), output signals of at least one PPG sensor (14) are processed to derive a modified pulse amplitude variation (PAV) value, being modified to take account of a baseline variation of the PPG sensor output signal. In particular, the modified PAV is derived through performing a modification step (42) in which either: a baseline variation of the PPG sensor output is derived and combined with a previously derived PAV, or, a PPG sensor output is first processed to perform baseline variation compensation, in advance of then deriving a PAV from the compensated signal.

Abstract: A method of detecting the likelihood of a seizure event in a patient includes at successive expirations of a first time interval, determining a first likelihood that the patient is experiencing a seizure based on electrodermal activity and a movement of a limb of the patient. The method also includes at successive expirations of a second time interval, determining whether the patient experienced a seizure in a second time period preceding the determining based on a heart rate of the patient. In response to determining that the third comparison result satisfies at least a third detection criterion, the method compares electrodermal activity and the movement of a limb of the patient to determine a second likelihood. In response to determining that the second likelihood satisfies a second detection criterion, the method triggers presentation of a second alert regarding a potential seizure.

Abstract: A component measurement device for measuring a given component contained in a sample. The component measurement device includes an excitation light source to emit excitation light onto the optical medium portion, a probe light source to emit probe light onto the optical medium portion, an intensity modulation unit to perform intensity modulation on the excitation light emitted by the excitation light source based on stratum corneum information about stratum corneum of the sample to generate intensity-modulated excitation light and emit the generated intensity-modulated excitation light onto the optical medium portion, and a measurement unit to measure the given component based on a difference between the probe light emitted from the optical medium portion in a first state where the excitation light is emitted and the probe light emitted from the optical medium portion in a second state where the intensity-modulated excitation light is emitted.

Abstract: A method for augmenting a real-world scene viewed through augmented reality (AR) glasses includes determining that an overlay should be processed for a real-world person being viewed via the AR glasses, with the determining using artificial intelligence (AI) to identify a trigger scenario. The AI is configured to process a video stream of images captured of the real-world person using a camera of the AR glasses to identify the trigger scenario, which is associated with an intensity level exhibited by the real-world person. The method also includes identifying the overlay to replace a portion of the real-world person in the video stream of images, and generating an augmented video stream that includes the video stream composited with the overlay. The augmented video stream being presented via the AR glasses is configured to adjust the intensity level exhibited by the real-world person when viewed via the AR glasses.

Abstract: An eyewear device, method for use with an eyewear device, and a non-transient computer readable medium for detecting blood sugar levels are disclosed. The eyewear device has a frame including a first rim configured to support a first lens, a second rim configured to support a second lens, and a bridge connecting the first rim to the second rim. The bridge is configured to receive a nose of a user when the eyewear device is worn by the user. Blood sugar levels are detected by monitoring behavior of a pupil of an eye of the user with a sensor, comparing the monitored behavior with known blood sugar level behaviors, identifying a match responsive to the comparison between the monitored behavior and one of the known blood sugar level behaviors corresponding to a particular blood sugar level, and selecting the particular blood sugar level as a blood sugar level of the user.

Abstract: Systems and methods for assisting user with hearing by amplifying sound using an amplifier with gain and amplitude controls for a plurality of frequencies; and applying a learning machine to identify an aural environment and adjust the amplifiers for optimum hearing.

Abstract: Systems and methods to determine a risk factor related to dehydration and thermal stress of a subject are disclosed. Exemplary implementations may: generate output signals, by one or more sensors worn on a body of a subject, conveying information related to one or more of location of the subject, motion of the subject, temperature of the subject, cardiovascular parameters of the subject; store information related to the subject; obtain the output signals; determine in an ongoing manner, from the output signals, values of a water loss metric that correlates with estimated percentage of bodyweight of the subject lost in water; obtain heat index information for a contextual environment surrounding the subject; determine in an ongoing manner, from the output signals, values of an exertion metric that correlates with exertion of the subject due to work; and determine in an ongoing manner values for an aggregated risk factor of the subject.

Abstract: A mobile device includes a connector, an audio generator, a biological signal processor, a switch element, and a controller. The switch element has a first terminal and a second terminal. The first terminal of the switch element is coupled to the connector, and the second terminal of the switch element is selectively coupled to either the audio generator or the biological signal processor according to a control signal. The controller is coupled to the audio generator and the biological signal processor, and is configured to generate the control signal.

Abstract: A method to analyze an eye with a mobile device includes capturing an eye image using a mobile device camera coupled to a processor; capturing gyroscope or accelerometer readings as image metadata to aid in orientation normalization and image registration by the processor; extracting features of the eye using the image corrected with image metadata; and applying the extracted features to a deep learning neural network to detect eye focus data or eye gaze data.

Abstract: The present disclosure relates to systems and methods for processing signals from wearable motion sensors associated with gait activity of a subject. In some cases, a signal representative of the gait activity of the subject may be received from the wearable motion sensors. One or more directional components of the signal, which are independent of an orientation of the wearable motion sensors on the subject, may be identified. One or more gait features may be extracted from the signal based on the one or more directional components of the signal. At least one of a diagnosis, a progression, a treatment, and a treatment response for a neurological dysfunction may be determined based on the one or more gait features.

Abstract: A wearable motion monitoring device including: a housing sized and shaped to be positioned between a body region of a subject and a garment worn by the subject; a marker included in the housing, the marker including at least one light emitter, wherein the light emitter is positioned to emit light from an upper surface of the marker, such that the at least one light emitter is indicative of displacements of the body region; and at least one garment holder incorporated in the housing, wherein the holder serves as an anchoring point between the marker and the garment, the garment overlying the marker when anchored by the at least one garment holder.

Abstract: The present disclosure relates to a subtle cornea deformation identification method and device based on a pixel-level corneal biomechanical parameter, including the following steps: step 1, sampling and analyzing a dynamic video of corneal stress deformation in a historical database, and calculating pixel-level data; and step 2, configuring an ensemble classifier based on a sampling result and detecting a local change in corneal biomechanics, thus identifying a subtle cornea deformation. The present disclosure has high measurement accuracy and is capable of detecting a local subtle biomechanical change.

Abstract: Exemplary methods are provided for real-time assessment of a potential risk of an infectious disease, including receiving a predetermined acceptable range for an aspect of a human user's physiological measurement data, receiving a predetermined acceptable answer for a survey response question, securely receiving an aspect of the human user's physiological measurement data, determining if the aspect of the human user's physiological measurement data is within the predetermined acceptable range, if the aspect of the human user's physiological measurement data is within the predetermined acceptable range, transmitting to the human user a survey comprising a question, if the aspect of the human user's physiological measurement data is not within the predetermined acceptable range, transmitting an active alert and not providing the human user with the survey comprising a question, and if the human user fails to transmit an acceptable answer to the survey comprising the question, transmitting an active alert.

Abstract: Disclosed is an isolated interface circuit for a modular energy system. A comparator is configured to couple to a switch and a reference voltage, and an output. A duplicate comparator is configured to couple to the switch and the reference voltage. An expander circuit is coupled to the comparator and the duplicate comparator. An isolator circuit is coupled to the expander circuit. A controller is coupled to the isolator circuit. The controller is configured to compare the output of the comparator with the output of the duplicate comparator and determine activation or deactivation of a surgical instrument coupled to the controller based on the comparison.

Abstract: A WCD system is configured to monitor various characteristics of the WCD system including about the patient. The WCD system is further configured to transmit a notification of a notifiable event to responders that are outside a local area of the patient, and to silence the notification for any responder(s) that are inside the local area of the patient.

Abstract: A method and apparatus for monitoring a subject's autoregulation function state is provided. The method includes: a) continuously sensing a tissue region of the subject with a tissue oximeter, the sensing producing first signals, and determining frequency domain tissue oxygen parameter values; b) continuously measuring a blood pressure level of the subject using a blood pressure sensing device, the measuring producing second signals, and determining frequency domain blood pressure values; c) determining a coherence value indicative of the subject's autoregulation state in each of a plurality of different frequency bands; and d) determining a peak coherence value indicative of the subject's autoregulation state based on the determined coherence value from each of the plurality of different frequency bands.

Abstract: A medical information processing apparatus according to an embodiment includes a processing circuitry. The processing circuitry is configured to: obtain first nerve activity information indicating an activity of a nerve of a subject; estimate first feeling information indicating a feeling experienced by the subject on the basis of the first nerve activity information; and determine presentation information to enable an evaluator to experience the feeling of the subject, on the basis of the first feeling information.

Abstract: A user environment is controlled and altered based on one or more user conditions received from a biometric tracking services associated with a biometric device of a user. A user can set up a user profile that includes one or more user preferences including a biometric parameter, an asset parameter, a biometric service parameter and/or a location parameter. Based on the user preferences a user device and/or an access point device can control the user environment by altering one or more assets of one or more network devices specified by any one or more user preferences. The asset state of an asset can be altered based on one or more user conditions associated with a biometric parameter such that the user environment is automatically altered based on monitoring the one or more user conditions so as to provide the user an enhanced user environment experience.