Abstract: A method for quantifying, during pacemapping, a comparison of a BSPM of interest to a pace site BSPM. The method may include receiving at a computing device a plurality of ECG signals from an acquisition system. The pace site BSPM may be calculated using the plurality of ECG signals. The BSPM of interest may be compared to the pace site BSPM, by: retrieving the BSPM of interest from memory accessible by the computing device; and, calculating one or more comparison metrics for the BSPM of interest as compared to the pace site BSPM. An indication of similarity between the BSPM of interest and the pace site BSPM based on the comparison metric calculated may be displayed on a user interface in communication with the computing device.

Abstract: A device for testing for the presence of neuropathy by applying a thermal stimulus to a test area of skin includes a temperature sensing arrangement for determining a reference temperature being a reference skin temperature or room temperature, a thermal stimulus application arrangement and a temperature controlling arrangement for controlling temperature of the thermal stimulus. The reference temperature is used in controlling the temperature of the applied thermal stimulus. The device may include a blood flow sensing arrangement which provides a measurement of blood flow in an area of the skin which may be considered to be indicative of a blood flow in response to an applied stimulus.

Abstract: A system comprises an external medical device configured to communicate with a first implantable medical device (IMD). The external medical device includes a communication circuit and a display. The communication circuit is configured to receive information associated with cardiovascular pressure from the IMD. The external medical device is configured to annotate a waveform on the display to indicate one or more events associated with cardiovascular pressure.

Abstract: The physiological detection device is for equipping on a user, and contains a physiological signal module, an impact module, and a tracking module. The impact module, the physiological signal module, and the tracking module are data-linked to each other. The physiological signal module and the tracking module are also data-linked to at least an alarm module. When the physiological signal module detects some abnormality, an alarm is automatically generated from the alarm module. When the impact module detects some abnormality, an alarm will not be generated immediately. Instead the tracking module monitors the physiological signal module for a period of time. In this way, the false alarm due to that the impact module detects abnormality whereas the user is actually all right. The present invention as such achieves automatic detection and avoids false alarm.

Abstract: A telepresence device may autonomously check patients. The telepresence device may determine the frequency of checking based on whether the patient has a risk factor. The telepresence device may include an image sensor, a thermal camera, a depth sensor, one or more systems for interacting with patients, or the like. The telepresence device may be configured to evaluate the patient's condition using the one or more sensors. The telepresence device may measure physiological characteristics using Eulerian video magnification, may detect pallor, fluid level, or fluid color, may detect thermal asymmetry, may determine a psychological state from body position or movement, or the like. The telepresence device may determine whether the patient is experiencing a potentially harmful condition, such as sepsis or stroke, and may trigger an alarm if so. To overcome alarm fatigue, the telepresence device may annoy a care provider until the care provider responds to an alarm.

Abstract: Implantable systems, and methods for use therewith, are provided for monitoring for an impending myocardial infarction. A signal indicative of changes in arterial blood volume is obtained. Such a signal can be a photoplethysmography signal or an impedance plethysmography signal. For each of a plurality of periods of time, a metric indicative of the areas under the curve of the signal or number of inflections in the signal is determined. An impending myocardial infarction is monitored for based on changes in the metric indicative of the area under the curve of the signal or number of inflections in the signal, and an alert and/or therapy is triggered in response to an impending myocardial infarction being predicted.

Abstract: A system and method for evaluating a patient status from sampled physiometry for use in heart failure assessment is presented. Physiological measures, including at least one of direct measures regularly recorded on a substantially continuous basis by a medical device and measures derived from the direct measures are stored. At least one of those of the physiological measures, which relate to a same type of physiometry, and those of the physiological measures, which relate to a different type of physiometry are sampled. A status is determined for a patient through analysis of those sampled measures assembled from a plurality of recordation points. The sampled measures are evaluated. Trends that are indicated by the patient status, including one of a status quo and a change, which might affect cardiac performance of the patient, are identified. Each trend is compared to worsening heart failure indications to generate a notification of parameter violations.

Abstract: A system and method for evaluating a patient status from sampled physiometry for use in heart failure assessment is presented. Physiological measures, including at least one of direct measures regularly recorded on a substantially continuous basis by a medical device and measures derived from the direct measures are stored. At least one of those of the physiological measures, which relate to a same type of physiometry, and those of the physiological measures, which relate to a different type of physiometry are sampled. A status is determined for a patient through analysis of those sampled measures assembled from a plurality of recordation points. The sampled measures are evaluated. Trends that are indicated by the patient status, including one of a status quo and a change, which might affect cardiac performance of the patient, are identified. Each trend is compared to worsening heart failure indications to generate a notification of parameter violations.

Abstract: Methods, systems and related apparatus are provided for controlling an electronic device to operate an external sensor connectable to an audio interface of the electronic device by applying a first harmonic driving signal to a first contact and a second harmonic driving signal to a second contact of the audio interface for driving the external sensor, receiving a response signal at a third contact of the audio interface, adjusting at least one of the first and second harmonic driving signals, determining one or more physiological parameters based on characteristics of the first and second harmonic driving signals and the response signal, and outputting the determined one or more physiological parameters.

Abstract: The subject invention is a Patient Care Monitoring System which employs a novel method and system for monitoring the care provided to a patient at a health care facility. In one embodiment, the subject invention includes a central processor in communication with a health care facility's computer systems, receiving data therefrom. This data is arranged and correlated to enable the subject invention to filter through the data and detect if a particular treatment, diagnostic test, or course of action has been or is in danger of being overlooked.

Abstract: A dive computer system that utilizes a direct skin temperature measurement is provided. The dive computer system includes a measurement device that includes a temperature sensor and is attached to a strap. The strap is placed around a diver's chest and configured to measure the diver's skin temperature. The skin temperature is wirelessly transmitted to a dive computer that utilizes a dive algorithm to determine compartment inert gas saturation and desaturation. The dive algorithm determines an updated skin perfusion factor that is in turn utilized to determine an updated half time for the skin compartment for inert gas desaturation and a pressure tolerance for the skin compartment for inert gas saturation.

Abstract: A biometric monitoring device measuring various biometric information is provided that allows the person to take and/or display a heart rate reading by a simple user interaction with the device, e.g., by simply touching a heart rate sensor surface area or moving the device in a defined motion pattern. Some embodiments of this disclosure provide biometric monitoring devices that allow a person to get a quick heart rate reading without removing the device or interrupting their other activities. Some embodiments provide heart rate monitoring with other desirable features such as feedback on data acquisition status.

Abstract: Characteristics of a user's heart are detected. In accordance with an example embodiment, a ballistocardiogram (BCG) sensor is used to detect heart characteristics of a user, and provide a BCG output indicative of the detected heart characteristics. The BCG output is further processed using data from one or more additional sensors, such as to reduce noise and/or otherwise process the BCG signal to characterize the user's heart function.

Abstract: A cognitive function evaluation method and system involves prompting a test subject (person) to engage in movement, such as whole-body movement, for example sports-specific movement, while tracking movement of the person. Data can be gathered from the tracking of the person's movement. This data can be compared with baseline data from an earlier test (or with data gathered from other subjects), to make a determination of cognitive function of the test subject, or to evaluate progress in rehabilitation and/or aid in making a determination whether a person is ready to resume specified activities, such as an athlete returning to a sport. Such a determination can be made under realistic activity-specific conditions (for example using increased metabolic rate and/or activity-specific movements that may test/challenge the test subjects cognition, vestibular, and/or visual performance/abilities), to allow a for determination of the person's cognitive function.

Abstract: An apparatus for estimating an anaerobic threshold may include a heart rate detector configured to detect a heart rate from a signal sensed from a user, and an anaerobic threshold estimator configured to estimate an anaerobic threshold of the user based on a change in the detected heart rate.

Abstract: A sensor assembly which includes a first physiological parameter sensor configured to sense a physiological parameter and a first reactance sensor connected to the first physiological parameter sensor. The first reactance sensor provides a signal corresponding to a position of a tissue relative to the first reactance sensor and corresponding to the first physiological parameter sensor.

Abstract: A method is provided of systematically evaluating and treating dynamic autonomic dysregulation in a subject. The method includes having the subject sequentially assume a plurality of distinct postures that may include, for example, walking, standing, sitting or supine. In each posture of the subject, the subject is subjected to sensory stimulation while measuring at least one autonomic physiological response of the subject. The autonomic physiological response may include, for example, oxygen saturation, heart rate, pupillary response, blood pressure, sweat production, pseudomotor activity or respiration. The physiological responses in each of the distinct postures are evaluated to identify a posture wherein the subject exhibits a least amount of dysfunction.

Abstract: A wearable device is disclosed configured to provide and transmit user information. Health-related information that is associated with a user information is received and output to a user. The wearable device can include a display configured to provide a user interface and a sensor senses information associated with biological features, physiological features and/or physical activity of the user, while the device is being worn. A communications subsystem is provided that is configured to communicate with the remote computing device. The wearable device includes a processing subsystem is provided and configured to process the sensed information to provide processed user information. The processed user information is transmitted via the communication subsystem, to the remote computing device, and health-related information associated with the processed user information is received from the remote computing device. The health-related information is provided, via the user interface, on the display.

Abstract: A multifunctional invasive cardiovascular diagnostic measurement host is disclosed that interfaces a variety of sensor devices, such as guide wire-mounted pressure sensors, flow sensors, temperature sensors, etc, and provides a multi-mode graphical user interface providing a plurality of displays in accordance with the various types of sensors and measurements rendered by the sensors.

Abstract: A system and method for evaluating a patient status from sampled physiometry for use in heart failure assessment is presented. Physiological measures are stored, including at least one of direct measures regularly recorded on a substantially continuous basis by an implantable medical device for a patient and measures derived from the direct measures. At least one of those of the physiological measures, which each relate to a same type of physiometry, and those of the physiological measures, which each relate to a different type of physiometry are sampled. A status for the patient is determined through analysis of the sampled physiological measures assembled from a plurality of recordation points. The sampled physiological measures are evaluated. Trends that are indicated by the patient status, which might affect cardiac performance of the patient, are identified. Each trend is compared to worsening heart failure indications to generate a notification of parameter violations.

Abstract: A heart monitoring system for a person includes one or more wireless nodes; and a wearable appliance in communication with the one or more wireless nodes, the appliance monitoring vital signs.

Abstract: Contact pressure sensing apparatus for use with exercise equipment sensors are described. An example apparatus includes a sensor to detect a physiological condition of a user of an exercise device through physical contact with the user and a pressure sensor to detect a contact pressure applied by the user to the sensor.

Abstract: Risk determination for a near fatal ventricular arrhythmia of a patient. An electrocardiogram of a heart of the patient is obtained. A parameter is measured, using an electrocardiogram of a heart of the patient, indicative of an autonomic nervous system of the patient. A numeric score is assigned for the parameter indicative of the conduction system of the heart. A numeric score is assigned for the parameter indicative of the autonomic nervous system. A ratio of the numeric score of the parameter indicative of the conduction system of the heart of the patient and the numeric score of the parameter indicative of the autonomic nervous system of the patient is calculated. The risk of the potentially near fatal ventricular arrhythmia of the patient is determined to be significant if the ratio is greater than a predetermined threshold. An action responsive to the determining step is taken.

Abstract: A method and system for measuring psychological stress disclosed. In a first aspect, the method comprises determining R-R intervals from an electrocardiogram (ECG) to calculate a standard deviation of the R-R intervals (SDNN) and determining a stress feature (SF) using the SDNN. In response to reaching a threshold, the method includes performing adaptation to update a probability mass function (PMF). The method includes determining a stress level (SL) using the SF and the updated PMF to continuously measure the psychological stress. In a second aspect, the system comprises a wireless sensor device coupled to a user via at least one electrode, wherein the wireless sensor device includes a processor and a memory device coupled to the processor, wherein the memory device stores an application which, when executed by the processor, causes the processor to carry out the steps of the method.

Abstract: One disclosed method involves using at least one device supported by a user while the user is in locomotion on foot during an outing to automatically measure amounts of time taken by the user to complete respective distance intervals. During the outing, data representing the automatically measured amounts of time may be automatically stored in memory of the least one device. Another disclosed method involves using at least one device supported by a user while the user is in locomotion on foot during an outing to automatically identify occasions on which a user completes respective distance intervals. During the outing, the at least one device may display at least one of an average pace of the user since a most recently completed distance interval, an average speed of the user since the most recently completed distance interval, and a projected time to complete a current distance interval based on monitored performance since the most recently completed distance interval.

Abstract: A composite manual and automated fetal strip analysis system is disclosed. A computer is configured to receive at least one of a signal indicative of said physiological parameter of a fetus and a signal indicative of uterine activity and automatically detect a pre-determined pattern. A user interface allows a user to manually alter results of the automatic detection.

Abstract: A medical device communication system is described. The system includes a plurality of medical devices, a message listener programmed to wirelessly receive a plurality of messages from the plurality of medical devices, a storage device in communication with the message listener for storing the messages, a message distribution device for delivering the messages to a plurality of locations including a system database, an analytics database, and an integration engine. The system is configured such that the system database performs extract, transform, and load operations to generate system specific message objects configured to include the received message used to generate the system specific message object, the analytics database computes and displays a real time analytic information stored in each system specific message objects, and the integration engine is programmed to transmit the system specific message objects and receive a plurality of feedback from a central information system.

Abstract: This document discusses, among other things, a system comprising a sensor signal processor configured to receive a plurality of electrical sensor signals produced by a plurality of sensors and at least one sensor signal produced by an implantable sensor, a memory that includes information indicating a co-morbidity of a subject, a sensor signal selection circuit that selects a sensor signal to monitor from among the plurality of sensor signals, according to an indicated co-morbidity, a threshold adjustment circuit that adjusts a detection threshold of the selected sensor signal according to the indicated co-morbidity, and a decision circuit that applies the adjusted detection threshold to the selected sensor signal to determine whether an event associated with worsening heart failure (HF) occurred in the subject and outputs an indication of whether the event associated with worsening HF occurred to a user or process.

Abstract: Systems, methods and devices for reducing noise in cardiac monitoring including wearable monitoring devices having at least one electrode for cardiac monitoring; in some implementations, the wearable device using a composite adhesive having at least one conductive portion applied adjacent the electrode; and, in some implementations, including circuitry adaptations for the at least one electrode to act as a proxy driven right leg electrode.

Abstract: A method and system for continually monitoring oxygenation levels in real-time in compartments of an animal limb, such as in a human leg or a human thigh or a forearm, can be used to assist in the diagnosis of a compartment syndrome. The method and system can include one or more near infrared compartment sensors in which each sensor can be provided with a compartment alignment mechanism and a central scan depth marker so that each sensor may be precisely positioned over a compartment of a living organism. The method and system can include a device for displaying oxygenation levels corresponding to respective compartment sensors that are measuring oxygenation levels of a compartment of interest. The method and system can also monitor the relationship between blood pressure and oxygenation levels and activate alarms based on predetermined conditions relating to the oxygenation levels or blood pressure or both.

Abstract: The present specification discloses methods and systems for synthesizing electrocardiographic (ECG) signals. In one method, a first group of electrodes are attached to predetermined locations on the human body. A posture sensor is attached to the human body and generates data indicative of the human body's posture. The system receives signals from the first group of electrodes connected to the predetermined locations on a human body and acquires a first set of ECG signals. The system then derives at least one further ECG signal by applying transformation(s) on the first set of ECG signals, or a subset thereof, to form a desired set of signals, where the applied transformations are selected based on the human body's posture.

Abstract: A biological condition evaluation apparatus determines a symptom of a heart abnormality based on at least one index calculated from a heartbeat interval and/or a pulse interval. The apparatus determines whether it is in a referential period where an amount of change in the index is comparatively small. The apparatus determines whether a plurality of conditions are satisfied or not in an evaluation period set after the referential period. One condition is that an amount of change in the index in the evaluation period is greater than that observed during the referential period. Another condition is that a rate of change in the index is equal to or greater than a predetermined threshold value. The apparatus determines that there is a symptom of a heart abnormality, when both the conditions are satisfied.

Abstract: A medical monitoring device for monitoring electrical signals from the body of a subject is described. The medical monitoring device monitors electrical signals originating from a cardiac cycle of the subject and associates each cardiac cycle with a time index. The medical monitoring device applies a forward computational procedure to generate a risk score indicative of hyperkalemia, hypokalemia or arrhythmia of the subject. The medical monitoring device can adjust the forward computational procedure based upon clinical data obtained from the subject.

Abstract: The invention relates to a fever detection apparatus for detecting fever of a living being. A heart rate providing unit (3) provides a heart rate value and a peripheral physiological value providing unit (3) provides a peripheral physiological value, wherein a heart rate characteristics determination unit (4) determines heart rate characteristics from the heart rate value and a peripheral characteristics determination unit (5) determines peripheral characteristics from the peripheral physiological value. A fever detection unit (6) detects fever depending on the heart rate characteristics and the peripheral characteristics. Since the heart rate characteristics and the peripheral characteristics are influenced by fever, the fever detection apparatus can be used to reliably and preferentially unobtrusively detect fever.

Abstract: A method of predicting an onset of apnea is described. Motion of a subject, including at least breathing-related motion, is sensed, and a signal corresponding to the sensed motion is generated. A breathing-related signal is extracted from the sensed motion signal, and the onset of apnea is predicted at least partially in response to analyzing the breathing-related signal. Other applications are also described.

Abstract: Methods and apparatus provide a wireless electrode having energy conservation. In one embodiment, a wireless electrode includes a radio module coupled to the sensor to wirelessly transmit the cardiac information, an energy source to power the radio module, and an activation mechanism coupled to the energy source, the activation mechanism having an activated state in which power from the energy source is delivered to the radio module and a non-activated state in which power from the energy source is not delivered to the radio module.

Abstract: An apparatus and a method for determining the volume amount of a physiological volume (EVLW) from the system response to two successive system disturbances, taking into account that an intrinsic physical property of the physiological volume is influenced by the first (or previous, respectively) system disturbance, is described. By introducing a cold bolus to the central venous blood stream, a flowed-by volume, such as extravascular lung water, is cooled down. The driving temperature gradient for heat transfer is reduced when a second cold bolus is introduced. From the difference of the system response to the first bolus injection and the second bolus injection EVLW can be determined.

Abstract: An exercise information detecting apparatus of the present invention includes a heartbeat sensor which detects heartbeat data of a human body including a waveform signal, an exercise status detecting section which detects exercise data regarding an exercise status of the human body, an exercise status judging section which judges a change of the exercise status of the human body based on the exercise data detected by the exercise status detecting section, and a heart rate calculating section which removes, as a noise component, an invalid peak from among a plurality of peaks included in the waveform signal of the heartbeat data based on the change of the exercise status of the human body judged by the exercise status judging section.

Abstract: Non-invasive sensor apparatus and method for assessing cardiac performance. A wide variety of different sensor components can capture sensor readings relating to patient attributes. Those sensor readings can then be compared by a processor component to derive a cardiac performance indicator relating to the patient.

Abstract: Apparatus is provided, including a sensor, adapted to generate a sensor signal indicative of biorhythmic activity of a user of the apparatus, the sensor signal having a first characteristic, indicative of a voluntary action of the user, and a second characteristic, indicative of a benefit-related variable of the user. The apparatus also includes a control unit, adapted to receive the sensor signal, and, responsive to the second characteristic, generate an output signal which directs the user to modify a parameter of the voluntary action indicated by the first characteristic.

Abstract: Pressure sensing devices for use with an inflatable bladder and monitoring apparatus for an at rest subject are disclosed herein. The device can comprise a housing comprising a recess and configured to be welded in a seam of the inflatable bladder. A pressure sensor can be located within the recess with a sensing side configured to be exposed to the cavity of the inflatable bladder and a reference side configured to be exposed to ambient air. A printed circuit board can be located within the recess and coupled to the pressure sensor. The pressure sensor is operable to detect a pressure change within the cavity due to a force exerted by a subject on the inflatable bladder.

Abstract: An example system and method of processing cardiac activation information are disclosed. The method includes accessing a first cardiac signal and a second cardiac signal obtained from a patient. The first cardiac signal and the second cardiac signal are processed to determine whether there is a point of change in the first cardiac signal at which a derivative of the first cardiac signal diverges with respect to a derivative of the second cardiac signal above a threshold. An activation onset time is assigned in the first cardiac signal at the point of change to define a cardiac activation if the point of change is in the first cardiac signal.

Abstract: A data collection module receives signals generated using at least one of an electromyography (EMG) sensor connected to a user, an electroencephalography (EEG) sensor connected to the user, an electrocardiogram (ECG) sensor connected to the user, and an oxygen saturation (SPO2) sensor connected to the user. A mobile computing device is implemented independently of the data collection module and communicates with the data collection module. The mobile computing device includes a processor and a tangible computer readable medium including a sleep study application embodied as code for: selectively prompting the data collection module to store data samples generated based on the signals; receiving the data samples from the data collection module; and transmitting sleep study data including the data samples to a first data server. The mobile computing device further includes a communications module that wirelessly downloads the sleep study application from a second data server.

Abstract: An apparatus and method for obtaining one or more physiological measurements associated with a user using ear-located sensors is disclosed herein. One or more of different types of sensors are configured to engage a user's ear. In some cases, the sensors will be included in one or both of a pair of earphones to capture physiological parameters. A portable device is configured to be in communication with the earphones to receive physiological parameters from the sensor(s) therein, and to potentially provide control signals to the sensors or other components in the earphones. The portable device determines physiological measurements corresponding to the received physiological parameters. The portable device is also configured to provide a user interface to interact with the user regarding the physiological measurements.

Abstract: A mobile computing device for performing a sleep study includes a processor, a tangible computer readable medium, and a communications module. The tangible computer readable medium includes a sleep study application embodied as code for: selectively prompting a data collection module to store data samples generated based on signals generated using at least one of an electromyography (EMG) sensor connected to a user, an electroencephalography (EEG) sensor connected to the user, an electrocardiogram (ECG) sensor connected to the user, and an oxygen saturation (SPO2) sensor connected to the user; receiving the data samples from the data collection module; and transmitting sleep study data including the data samples to a first data server. The communications module wirelessly downloads the sleep study application from a second data server.

Abstract: A data collection module for performing a sleep study is described. The data collection module includes a first module, a second module, and a collection control module. The first module receives an electrocardiogram (ECG) signal from an ECG sensor connected to a user. The second module receives an electroencephalography (EEG) signal from an EEG sensor connected to the user. The collection control module: communicates with a mobile computing device; in response to a prompt from the mobile computing device, stores data samples generated based on the ECG and EEG signals in a tangible computer readable medium; and selectively transmits the data samples to the mobile computing device.

Abstract: An implant predicts decompensation of a patient's heart based on an acoustic pressure measurement. The implant includes first and second acoustic transducers, which are matched to each other and which rest in/on the patient's thorax. The first acoustic transducer emits an acoustic signal which has at least one first signal portion having a first frequency. The second acoustic transducer is designed to receive and re-emit the emitted acoustic signal, or to reflect it, such that the first acoustic transducer receives the emitted acoustic signal. A signal processing unit communicates with at least one of the two acoustic transducers and determines an attenuation value as a function of the attenuation of the received acoustic signal versus the originally emitted acoustic signal, and provides a prediction signal as a function of a comparison of the attenuation value to a threshold value, wherein the prediction signal indicates the development of decompensation.

Abstract: A method for measuring human vital signs and a portable terminal adopting the same provides accurate measurements without increasing the thickness of power usage of the portable terminal. The portable terminal includes: a surface acoustic wave (SAW) sensor module disposed on a predetermined position of a portable terminal main body to detect characteristic parameter of human body; a signal transceiving module used to perform communication with the SAW sensor module, to receive an echo signal of the SAW sensor module; and a data processing module used to process the echo signal from the SAW sensor module to obtain the human vital signs. The SAW sensor module includes a sensing unit that does not require receiving power from a power supply for operation when implemented as a passive element.

Abstract: This document discusses, among other things, a system comprising an implantable medical device (IMD) including an implantable heart sound sensor circuit configured to produce an electrical heart sound signal representative of a heart sound of a subject and a processor circuit. The processor circuit is coupled to the heart sound sensor circuit and includes a detection circuit, a heart sound feature circuit and a trending circuit. The detection circuit configured to detect a physiologic perturbation and the heart sound feature circuit is configured to identify a heart sound feature in the electrical signal. The processor circuit is configured to trigger the heart sound feature circuit in relation to a detected physiologic perturbation. The trending circuit is configured to trend the heart sound feature in relation to a recurrence of the physiologic perturbation. The processor circuit is configured to declare a change in a physiologic condition of the patient according to the trending.

Abstract: The present subject matter relates to a computer implemented method for real time determination of stress levels of an individual. The method includes receiving at least one stream of physiological data from at least one primary sensor for a predetermined duration, and preprocessing the at least one stream of physiological data to extract physiological parameters, where the preprocessing includes performing a preliminary analysis on the at least one stream of physiological data. The method further includes determining a stress level of the individual based on at least the physiological parameters, wherein the determining comprises performing a statistical analysis on the physiological parameters.