825 results about "CLOCK" patented technology

A system for acquiring, and displaying, data such as physiological data, from a plurality of data connection devices, each of which monitor one or more different parameters and output data at different sampling frequencies based on their own system clocks. The system receives the data signals at different sampling frequencies and associates each sample of each signal with a time stamp derived from a single master clock. Low rate and high rate data are treated differently. Low rate data is associated with the current value of the master clock, where as high rate data is time stamped by giving the first sample a time stamp equal to the current value of the current master clock, subsequent samples being given an estimated time stamp based on the expected interval between samples derived from the sampling frequency of the data collection device, and the timescale given to the first example. The estimated time stamp may be periodically corrected, and the estimation calculation can be improved by correcting the value used for the interval between samples. The different signals can be displayed together on a display aligned with respect to a time axis. The system can display, the data in two different timescales, one showing a few seconds of data and one showing a few hours of data. The data traces are scrolled across the time axis, new data being added to one end of the trace.

A neural prosthesis includes a centralized device that can provide power, data, and clock signals to one or more individual neural prosthesis subsystems. Each subsystem may include a number of individually addressable, programmable modules that can be dynamically allocated or shared among neural prosthetic networks to achieve complex, coordinated functions or to operate in autonomous groups.

A physiological parameter measurement and motion tracking system including a control system, a sensing system, and a stimulation system is disclosed. The sensing system includes one or more physiological sensors including at least brain electrical activity sensors. The stimulation system includes one or more stimulation devices including at least a visual stimulation system. The control system includes an acquisition module configured to receive sensor signals from the sensing system, and a control module configured to process the signals from the acquisition module and control the generation of stimulation signals to one or more devices of the stimulation system. The control system further includes a clock module and the control system is configured to receive content code signals from the stimulation system and to time stamp the content code signals and the sensor signals with a clock signal from the clock module.

A method and system for monitoring and/or controlling a glycemic state of a subject, comprising a housing device having one or more chambers, extendable and retractable sensors, extendable and retractable catheters, insulin reservoir, neuroprotective agent reservoir, release mechanism for releasing insulin and neuroprotective agent into the subject, and a control mechanism with a processor for receiving and analyzing outputs from the sensors and for controlling the release mechanism, a clock mechanism for providing logging and/or circadian information to the processor, an internal analysis chamber, a byproduct storage chamber, a sampling mechanism, a transfer mechanism, a self-sealing membrane, a calibration chamber, a replacement sensor chamber, a prevention mechanism to prevent deposition of unwanted substances on a sensor or catheter, a removal mechanism to remove unwanted substances from a sensor or catheter, a warning mechanism, a real-time clock and non-volatile memory to store and log information processed by the processor, a failure detection mechanism, and wired and/or wireless communication linkages both internally and externally.

An implantable medical device, external unit, and method for establishing communication between them are disclosed. The external unit learns the frequencies of transmission and reception for the implant. The transmit frequency of the implant is learned by the external unit measuring a difference between the transmit frequency of the implant and the external unit's receive frequency. The receive frequency of the implant is learned by the measured difference between its transmit frequency and the receive frequency of the external unit when the implant has a fixed transmit and receive frequency difference. Otherwise, the receive frequency is learned by the implant measuring the difference between its receive frequency and the transmit frequency of the external unit and by sending an indication of the difference to the external unit through the return signal. The external unit may anticipate a beginning of the implant's preset communication period based on its internal clock.

A user's personal biometric information such as age, sex, weight, height as well as the user's lifestyle information, such as daily caloric input, job description, smoker status and physical fitness, is uploaded onto a host computer. Target heart rate, energy and/or caloric consumption levels related to desired fitness and weight loss goals for a particular individual are then selected having regard to fitness levels for an individual of comparable age, and consuming similar calories are then downloaded to a caloric monitoring unit. The caloric monitoring unit is provided for measuring the user's heart rate and dynamic energy and/or caloric expenditure over one to four weeks. The caloric monitoring unit includes a heart rate monitor, a unit accelerometer, a global positioning system (GPS), and an audio and/or video output. The audio/video output is operable to provide information and/or motivational prompts to the user in the event the heart rate, energy expenditure and/or caloric expenditure falls below or exceeds pre-selected target expenditures over a particular time segment of the selected time period having regard to the calories which are consumed. A display provides a continuously updated visual indication of whether or not the use has achieved the pre-selected optimum caloric burn or energy expenditure for that particular time segment. An internal calendar/clock, a processor and/or memory in the caloric monitoring unit compares measured heart rate and energy expenditures for multiple time segments against target levels stored as the user-specific fitness programme tailored to achieve the desired weight loss. The comparison is then used to generate compliance output data to either the user and/or a nutritionist.

Efficient and effective mechanisms for collecting electroencephalography (EEG) data are provided to synchronize neuro-response data collection with stimulus material presentation for in situ engagement monitoring and tracking. An EEG headset includes multiple point electrodes individually isolated and amplified. In some examples, a stimulus material presentation mechanism includes a clock source and a clock transmitter. The clock transmitter sends clock signals to a neuro-response data collection mechanism to allow synchronization of neuro-response data collected with stimulus presentation events. The EEG headset can be configured to perform processing while supporting both continuous input and output.

The invention discloses a continuous Doppler US imaging system orthogonal intrinsic signal generation device, which comprise a field programmable gate array (FPGA), a crystal oscillator, a first digital-analog converter and a second digital-analog converter. The output end of the field programmable gate array (FPGA) is connected with the input ends of the first digital-analog converter and the second digital-analog converter; the crystal oscillator is respectively connected with the field programmable gate array (FPGA), the first digital-analog converter and the second digital-analog converter; the crystal oscillator is used for supplying synchronizing clock signals to the field programmable gate array (FPGA), the first digital-analog converter and the second digital-analog converter; the field programmable gate array (FPGA) is used for outputting the sine value corresponding to the phase value to the first digital-analog converter according to the input phase value and outputting the cosine value corresponding to the phase value to the second digital-analog converter; the first digital-analog converter is used for converting the sine value into the corresponding analog signals; the second digital-analog converter is used for converting the cosine value into the corresponding analog signals.

A medication-taking confirmation support device includes a pill case having a pill housing section, an electronic clock equipped with a memory, a notification unit and a controller, a pill case open/close sensor, and a reconfirmation signal input device. The controller makes the notification unit notify a medication-taking confirmation time on the basis of a detection signal from the pill case open/close sensor and also makes the memory store the medication-taking confirmation time at the time of taking medication. The controller further makes the notification unit re-notify the medication-taking confirmation time read out from the memory on the basis of a signal from the reconfirmation signal input device after having taken medication.

A cyclic redundancy code (CRC) and optionally a syndrome value calculation of one or more implantable medical device (IMD) data block is conducted by block mover/reader hardware of the IMD when the data block(s) are moved and/or read. In the block read operation, each data byte or word in the block mover data register is read in a first clock cycle. In the block move operation, each data byte is read in the first clock cycle in this way and then moved to a destination register in a second clock cycle. The data CRC and optionally the syndrome value accumulate in the CRC and syndrome registers as all data bytes of the data block(s) are read in the first clock cycle. When the last data byte or word of the data block(s) is sequentially read (and moved in the block move operation), the accumulated data CRC and syndrome value are either stored as the associated data CRC and optional syndrome value or are used for comparison with a previously stored data CRC and optional syndrome value associated with the data block(s) in the comparison operation to determine if the data block(s) is corrupted.

Systems, devices, and methods for more accurately determining a radiopharmaceutical dose administered to a patient by relying on a time factor. Particularly, broadly contemplated herein is the administration of a dose on the basis of an elapsed time from when a dose was last accurately measured in the past to when it is injected into the patient. As such, when a dose is first measured, that timepoint is preferably recorded whereupon the time of injection or administration into a patient is also recorded. Based on the original measured dose, the radionuclide (and thus its known decay rate) and the time elapsed, the dose is calculated and not directly measured on injection. The clocks on the filling station and the transport cart are synchronized to each other or to a known and accepted time standard. In this manner, there is temporal continuity and no inaccuracies of time or loss of time occurs between measurement and injection.

A tamper monitor circuit detects voltage, temperature, and/or clock variations that may be associated with a circuit tampering technique, and triggers an appropriate tamper response. The tamper monitor circuit includes a reference oscillator, a detection oscillator, and a comparison circuit. The reference oscillator supplies a reference signal having a reference frequency. The detection oscillator operates at a circuit temperature and is energized with a supply voltage, and supplies a detection signal having a frequency that varies with variations in the circuit temperature, variations in the supply voltage, or both. The comparison circuit receives the reference signal and the detection signal and, in response to the reference signal, selectively determines the frequency of the detection signal, determines a frequency difference between two or more of the determined frequencies, and supplies a tamper detect signal if the determined frequency difference exceeds a predetermined difference threshold.

A toothbrush for setting and communicating brushing time and for providing instructional and encouragement messages during brushing includes a handle with a hollow interior, a controller capable, upon activation, of generating such messages, a power source electrically connected to the controller, a speaker for emitting such messages and a switch for activating the controller and enabling the speaker to emit the messages. A timer is provided to terminate operation of the speaker after a predetermined amount of time. A digital or a conventional clock is disposed on the surface of the handle and cooperates with the timer for visual communication of the elapsed brushing time.

An automated pet food dispenser is described that comprises a rotatable food chamber with multiple cavities to hold food for different meals, a base unit for supporting the food chamber, a rotary mechanism to rotate the food chamber relative to the base, and a timing mechanism that indicates feeding times. At feeding times, the rotary mechanism rotates the food chamber to position a selected cavity such that food stored in the cavity may drop out of an opening in the cavity, preferably through a chute or channel, and into a feeding station positioned below. A control unit in the automated pet food dispenser may be configured to initiate anti-jamming procedures if food becomes jammed and obstructs the rotation of the food chamber. In various embodiments, feeding times may be set to occur at fixed time intervals or may be set to occur at times set on a programmable clock on the base unit. In some embodiments, a recording mechanism in the automated pet food dispenser allows a user to record an audio clip such as a voice message, music, or other selected sound for calling a pet to eat at feeding times.

A device external to an implantable medical device (IMD) is provided with an accurate reference clock. The programmer receives time data from the IMD and compares that data to time data from the reference clock. Based on this comparison, the programmer determines how much a clock within the IMD is drifting per unit of time. A correction factor is generated so that data received from the IMD can then be correlated to the correct reference time.

A drug infusion assembly comprises a drug delivery device arranged to adhere to a patient's skin and includes a reservoir that holds the drug, a cannula that delivers the drug to the patient, and a pump that causes the drug to flow to the cannula. The assembly further includes a monitor device for providing information about the operation of a drug delivery device. The monitor device includes a housing arranged to be attached to and detached from the drug delivery device, a sensor that senses the operation of the drug delivery device and generates an activation signal, a clock mechanism that generates a time signal, a memory that receives and stores the activation signal and the time signal and creates an information packet coordinating the time signal and the activation signal, an interrogator that interrogates the memory such that the memory generates a memory signal in response thereto, and a responder that receives the memory signal and generates a response.

The invention discloses a bracelet capable of collecting multi-parameter health indexes. The bracelet comprises a body and a wrist strap. The body comprises a shell body, a displaying screen, a power supply, a clock part and a main control system. The displaying screen, the power supply, the clock part and the main control system are arranged in the shell body. The main control system comprises a main printed board, a microprocessor, a storage, an analogue signal processing chip and a Bluetooth transmission device. The microprocessor, the storage, the analogue signal processing chip and the Bluetooth transmission device are arranged on the main printed board. An infrared temperature sensor, an alarming device, a gravitational acceleration sensor for step counting and a charging connector are arranged on the main printed board. A flexible connecting wire cable, a measuring printed board, a body surface temperature sensor, a photosensitive sensor and a light source are arranged on the wrist strap. The body surface temperature sensor, the photosensitive sensor and the light source are integrated on the measuring printed board. A tensioning device is arranged on the wrist strap. The bracelet is small and light, wearing and using are convenient, various health parameters can be monitored accurately, human body parameters are collected near the Neiguan point under a wrist of a palm side, the number of blood vessels under the wrist is large, pulsation is obvious, and accordingly the accuracy of data testing and obtaining through the bracelet is greatly improved.

A blink detection algorithm and associated circuitry for an ophthalmic lens comprising an electronic system is described herein. The blink detection algorithm is implemented in the system controller which is part of an electronic system incorporated into the ophthalmic lens. The electronic system includes one or more batteries or other power sources, power management circuitry, one or more sensors, clock generation circuitry, control algorithms and circuitry, and lens driver circuitry. The blink detection algorithm implements the steps of sampling, at a predetermined rate, light incident on an eye of an individual and at least temporarily saving collected samples, determining when an eyelid is open or closed in order to divine the number, time period and pulse width of the blinks from the collected samples, calculating a number of blinks and the duration of the blinks in a given time period, and comparing the number of blinks, the durations of the blinks in the given time period, and the time between blinks in the given time period to a stored set of samples to determine patterns in blinking.

The invention discloses a method for grabbing a moving target by a vision-based hand-eye type low-servo precision robot, which is performed by the following: step 10, capturing the characteristic parameter of an image of a target object, and estimating the relative position between the target object and a camera; step 20, predicating the position of the target object in the next clock cycle ; and step 30, generating a track layout for grabbing of the moving target object, so that a controller of the robot can control a robot arm to approach the target object to realize grabbing. The method can generate a layout for the grabbing track of the moving object, thereby improving grabbing precision to finally realize grabbing of the moving object, and solving the technical difficulty of breaking through low-precision robot arm based on visual servo.

A patient monitoring device includes a microprocessor controller having a clock circuit and memory coupled to one or more sensors physically carried by a medical appliance such that as the medical appliance is properly fitted to and worn by the patient, the sensors provide an electrical signal confirming that which may be then timed to provide data which confirms a patient's compliance with a recommended protocol. By combining and correlating the sensor data with the clock or timer provided as part of the controller, a time chart of data may be created indicating when and for how long the patient actually wears the device. Additionally, other sensors may be used to collect data relating to various operational parameters of the device including the amount of negative pressure presented under a vacuum dome or other parameters related to the operation of the medical appliance itself, as desired.

A “medication communicator” chart is used as a teaching tool to educate patients and to schedule events corresponding to a prescribed medication regimen. The “medication communicator” chart includes a scheduling graph having the shape of a 12-hour or 24-hour analog clock. The scheduling graph is divided into regions corresponding to each hour of a day for scheduling event information. Fields, on the “medication communicator” chart, are receptive to labels communicating information corresponding to numerous medications in the medication regimen. Timing indicators may be applied to the regions of the scheduling graph to indicate consumption or application times of each of the medications.

The invention discloses a multiparameter biological information testing platform and a testing method, which adopts a movement human body as a testing object, acquires kinematic parameters, macroscopic action force of a human body and a supporting surface, distribution characteristics of sole pressure, bioelectric information of muscle groups of the human body and the like of all sections synchronously, monitors dynamic change characteristics of cardiopulmonary functions of the human body and provides theory and platform support for relevant studies and applications. The multiparameter biological information testing platform comprises a biological testing channel and integrated analysis software, wherein the testing channel comprises a synchronous clock server, a gait tactile information testing unit, a surface myoelectric acquisition unit, a high-speed image acquisition unit, an acceleration/angle testing unit and a heart rate/pulse testing unit. Under the uniform control of a center computer, all subfunction instruments are interconnected by an Ethernet interface, and realize accurate synchronization of time domains of all parameters by a clock synchronous server to form a comprehensive testing platform; each unit equipment also can be equipped with self-analysis software and a man-machine interface to form an independent instrument. The invention provides a multiparameter biological information acquiring integrated testing device and a testing method for the aspects of gait analysis, sports science research, movement function and health evaluation, basic tests and the like.