Abstract: The present invention generally relates to systems and methods for monitoring and/or providing feedback for drugs or other pharmaceuticals taken by a subject. In one aspect, the present invention is directed to devices and methods for determining a species within the skin of a subject; and producing feedback to a subject based on the determination of the species. The feedback may be, for example, visual, audible, tactile, a change in temperature, etc. In some cases, information regarding the determination of the species may be transmitted to another entity, e.g., a health care provider, a computer, a relative, etc., which may then provide feedback to the subject in some fashion. In some cases, the feedback may be directly indicative of the species. However, the feedback may also be indirect in some embodiments.

Abstract: Methods, systems, and computer program products are provided for measuring and analyzing muscle flexibility to infer a change in gait. Muscle flexibility measurements are obtained using at least one sensor of a device attached to a body of a user. A flexibility quotient is calculated based on the obtained muscle flexibility measurements, user information, a type of activity, a workout duration and baseline data. A change in flexibility based on the calculated flexibility quotient and a baseline flexibility quotient is determined. A change in gait is inferred based on the determined change in flexibility and is reported to the user.

Abstract: A sensor bed pad has a plurality of layers including an outermost layer made of a flexible material and a pair of inner layers, wherein each inner layer has an electrically conductive material thereon. A central layer is positioned between the pair of inner layers, wherein the inner layers are made of cloth, and wherein the central layer has a plurality of openings extending therethrough. The electrical conductive material of one of the inner layers contacts the electrical conductive material of the other inner layer through the openings in the central layer when a force is applied to the sensor bed pad to complete an electrical circuit between the inner layers.

Abstract: Embodiments of the invention are directed to systems, methods, and computer program products for collection of and utilization of electroencephalography (EEG) data for user experience and interaction management. The invention interconnects with a network for real-time user experience modification based on user identification via EEG data. In this way, upon recognition and analysis of EEG data, the invention forms and modify a user specific experience via integration within third party systems. EEG readings are segmented, sorted, and matched to a user baseline EEG reading to identify the user and modify the user experience based on quantifiable points.

Abstract: A disposable lancet assembly includes: a spring aligned along a linear axis; a lancet aligned along the linear axis adjacent to the spring; a needle cup aligned along the linear axis adjacent to the lancet; and a housing including a channel that accepts an actuator interface such that the needle cup and lancet are able to be moved along the linear axis via the actuator interface. A medical test cartridge includes: a bottom plate; a microfluidic chip; and a top plate, wherein the top plate is coupled to the bottom plate such that the microfluidic chip is retained between the top plate and the bottom plate. A sample collection and testing device includes: a lancet assembly; a lancet actuator coupled to the lancet assembly; and a microfluidic test chip.

Abstract: A system (100) for assessing a subject at risk of a soft tissue abnormality such as deep vein thrombosis (DVT), comprises a motion sensor (108) which is adapted to be fixed, in use, to a muscle (106) of the subject. The motion sensor includes a transmitter (206) configured to transmit a signal (400) representing motion of the sensor. A receiver (118) is configured to receive the signal from the transmitter of the motion sensor. A signal processor (112) is coupled to the receiver and configured to analyse first and second data sets received via the receiver from the motion sensor. The first and second data sets represent respective first and second oscillatory mechanical responses of first and second muscles of the subject resulting from mechanical stimuli. The analysis comprises determining first and second parameter sets characterising the first and second oscillatory mechanical responses, and comparing the first parameter set with the second parameter set to assess a possible presence of DVT in the subject.

Abstract: A system and method for collecting motion data using a fitness tracking device located on an arm of a user, detecting that the arm is constrained based on the motion data, estimating a stride length of the user based on the motion data and historical step cadence-to-stride length data, calculating fitness data using the estimated stride length, and outputting the fitness data to the user.

Abstract: A method for monitoring breathing air of a person breathing via a face mask (8). In the method pressure of inhaled air and partial pressure of oxygen before oxygen enters in the face mask (8) are measured. A partial pressure of oxygen in lungs of the person is estimated on the basis of the measured pressure of inhaled air and the measured partial pressure of oxygen. Also at least one physical characteristics of lungs is taken into account. The estimated partial pressure of oxygen in lungs is compared with a threshold. An indication of impending hypoxia is provided to the person, if the comparison indicates that the estimated partial pressure of oxygen in lungs is at a level lower than the threshold. The present disclosure also relates to an apparatus (6) for implementing the method.

Abstract: A method and system is provided for finding and analyzing gait parameters and postural balance of a person using a Kinect system. The system is easy to use and can be installed at home as well as in clinic. The system includes a Kinect sensor, a software development kit (SDK) and a processor. The temporal skeleton information obtained from the Kinect sensor to evaluate gait parameters includes stride length, stride time, stance time and swing time. Eigenvector based curvature detection is used to analyze the gait pattern with different speeds. In another embodiment, Eigenvector based curvature detection is employed to detect static single limb stance (SLS) duration along with gait variables for evaluating body balance.

Abstract: A flow rate control apparatus includes a flow rate detection unit that detects the flow rate of a fluid flowing through a solenoid valve, a correlation storage unit that stores a correlation between a flow start point voltage at which the fluid starts to flow through a sample solenoid valve, which has substantially the same characteristic as the solenoid valve, and a limit voltage at which the sample solenoid valve is fully open, and a control unit that, when starting control of the flow rate of the fluid, changes the driving voltage of the solenoid valve, obtains the driving voltage at a time when the start of flowing of the fluid is detected as the flow start point voltage, and uses the correlation for the sample solenoid valve to set the driving voltage of the solenoid valve within a range between the flow start point voltage and the limit voltage.

Abstract: An object is to provide programs for reliable predictions of the day of ovulation. A process is executed in a program for predicting a day of ovulation on a computer, the process including calculating a predicted ovulation day data corresponding to a particular menstrual cycle by applying the particular menstrual cycle to a relationship between a period between a menstrual day and a day of ovulation and an average length of a menstrual cycle, the relationship being estimated based on data of a plurality of persons which have been previously obtained.

Abstract: In various embodiments of the invention, a manipulator attaches to and allows a sheath to be positioned inside the cervix and a catheter to thereby be inserted through the sheath and be positioned in a desired location in the uterus. In various embodiments of the invention, the manipulator may be attached or permanently connected to the sheath. In various embodiments of the invention, the sheath is fenestrated to allow the catheter to be detached from the sheath. In various embodiments of the invention, the manipulator allows the sheath to be positioned through the cervix canal to allow for catheter transmitted intrauterine pressure monitoring or balloon catheter assisted ripening of the cervix.

Abstract: A medical sensor assembly comprises a flexible plaster adapted for adhesion on the skin of a patient and a sensor configured for transdermal measuring a physiological parameter, wherein the sensor has a measuring part insertable into the skin and a contact part for providing a signal connection to a measuring unit. It is proposed that the plaster has a flap which is adhered to an intermediate section of the sensor between the measuring part and the contact part.

Abstract: A biopsy needle has a cylindrical shell outer cannula and a stylet consisting of an inner stylet and outer stylet, both of which are inserted into the cylindrical cannula. The outer stylet has a series of strain relieved slits which provide bending over a deflection region in one direction, and the outer stylet is formed from a material such as a shape memory alloy (SMA) having a superelastic phase. The deflection is generated by an SMA wire spanning a deflection extent and attached to the outer stylet on either side of the deflection extent. The inner stylet, when positioned inside the outer stylet, has one or more actuation fibers which couple optical energy into the SMA wire or hollow SMA tube, causing a deflection of the outer stylet over the deflection extent, with the optical energy provided to the actuation fibers for control of the deflection. Additional fibers may be placed in the inner stylet to measure temperature and to measure deflection.

Abstract: Systems, methods, and devices for determining a temporal duration of a rest period using motion data are described herein. In one exemplary embodiment, one or more data filters are applied to received motion data to generate one or more data sets of the motion data. The motion data represents an amount of activity experienced by an individual over the course of a period of time, such as one day. An iterative process is performed to identify a starting point and an ending point of a rest period using the generated data set(s). After the starting and ending points are identified, a temporal difference between the starting and ending points is calculated, and a total temporal duration of the rest period is determined.

Abstract: An inventive medical device includes an implantable device, such as an electrochemical sensor. The implantable device has an implantable portion configured for insertion into a patient, a contact portion configured for connection to another device, and an interconnecting portion connecting the implantable portion and the contact portion. A housing is provided that has a first part that is removably connectable with a second part to form a sterile packaging to seal the implantable portion against a surrounding environment. The first part comprises a first sealing surface and the second part comprises a second sealing surface and the first and second sealing surfaces interact to form a sealing area. The interconnecting portion of the implantable device extends through the sealing area. An inventive method of producing the medical device is also disclosed.

Abstract: The invention relates to a device for posturography having a measuring platform, which comprises a standing surface for a test person having a base element on which the measuring platform is tiltably supported by means of a tilting apparatus, and having an air cushion means with which an air cushion bearing the base element is formed, wherein a damping member having a damping material is arranged between the measuring platform and the base element, by which damping member a tilting movement of the measuring platform is damped.

Abstract: A system for measuring and monitoring physiologically relevant motion of a subject includes at least a motion sensor to measure movement of the subject and produce a series of movement data representing the movement of the subject over a period of time. The system also includes at least a biometric sensor to simultaneously measure biometrics of the subject and produce a series of biometric values of the subject over the period of time. The system is configured to determine a noise-to-signal ratio for the series of movement data as a function of biometric intervals in the series of biometric values and identify at least a portion of the series of movement data as corresponding to a physiologically relevant biorhythm. The system can be used to diagnose and monitor a disease or disorder, including a neurological disorder or a traumatic brain injury.

Abstract: A method and device for identifying a human movement state that includes: determining according to acceleration signals that are collected by a three-axis acceleration sensor that a human is in a walking state, calculating a walking step number of the human, and calculating a walking step frequency according to the number; calculating a corresponding physical sign frequency during the walking process according to a physical sign signal that is collected; and comparing the walking step frequency and the physical sign frequency that are obtained by calculating respectively with a step frequency threshold and a physical sign frequency threshold, and if the walking step frequency is greater than the step frequency threshold, and the physical sign frequency is greater than the physical sign frequency threshold, determining that the human movement state is a running state, and recording the calculated walking step number to be a running step number.

Abstract: A needle assembly for sampling fluid from a patient including a needle guard, an insertion needle, and a needle housing. The distal end of the needle guard includes a nose portion and a flexible nose extension defining a fluid collection reservoir. The proximal end of the needle guard includes a push feature. The insertion needle has a sharpened distal tip, a proximal needle end and a shaft defining a lumen extending therebetween. The needle housing is operably coupled to the proximal needle end and is slideably coupled to the needle guard. The needle housing includes a flash chamber including a wall defining a cavity. The cavity is in fluid communication with the lumen of the insertion needle and is sealed at one end by a gas permeable flash plug. The push feature selectively engages the flash plug to divert captured bodily fluids to the fluid collection reservoir for sampling.