Abstract: A system includes a pulse generator including a can electrode and a lead couplable to the pulse generator, the lead including a distal coil electrode and a proximal coil electrode, wherein both of the coil electrodes are electrically uncoupled from the can electrode such that a unipolar sensing vector is provided between at least one of the coil electrodes and the can electrode.

Abstract: A holder for an implantable medical device (IMD) is disclosed. The holder is configured to hold the IMD in a single, operational orientation when the holder containing the IMD is implanted in a patient. The holder is designed to prevent the IMD from moving within the patient and shifting orientation. The holder may have an opening for receiving a connecting pin, for stimulating electrodes, for example, in a mating orientation with respect to a receptacle contained within the IMB. According to some embodiments, the IMB features a metal housing that can serve as an electrode and the holder is configured with a window to allow a portion of the housing to electrically contact flesh of a patient during operation. Holders for containing a single IMD and holders for containing multiple IMDs are disclosed. Holders for containing multiple IMDs are configured to maintain alignment of the IMDs with respect to each other, for example, a parallel alignment.

Abstract: A method and system for delivering a cardiac pacing therapy that includes a cardiac signal being sensed via electrodes of an atrial lead, and an occurrence of one of an intrinsic and a paced atrial depolarization event of a current cardiac cycle being determined in response to the sensed cardiac signal. A first pacing therapy is delivered during the current cardiac cycle in response to the determined occurrence of the depolarization event, and an amplitude of the cardiac signal within the current cardiac cycle subsequent to the delivered first pacing therapy is compared to a predetermined amplitude threshold. A second pacing therapy is delivered, via a left ventricular lead, within the same cardiac cycle and subsequent to the delivered first pacing therapy in response to the amplitude not being more negative than the predetermined amplitude threshold and is not delivered in response to the amplitude being more negative than the predetermined amplitude threshold.

Abstract: Embodiments describe herein generally pertain to implantable medical device (IMDs), and methods for use therewith, that can be used to automatically switch an IMD from its normal operational mode to an MRI safe mode, and vice versa, within increased specificity. In certain embodiments, a controller of the IMD uses a magnetic field sensor to determine whether a first magnetic field condition is detected, and uses an accelerometer to determine whether a positional condition is detected. In response to the first magnetic field condition being detected, and the positional condition being detected, the controller can use the magnetic field sensor to determine whether a second magnetic field condition is detected, which differs from the first magnetic field condition. The controller can then cause the IMD to enter the MRI safe mode based at least in part on the first and second magnetic field conditions and the positional condition being detected.

Abstract: A filter feedthrough for an AIMD includes an electrically conductive ferrule. An insulator hermetically seals a ferrule opening with either a first gold braze, a ceramic seal, a glass seal or a glass-ceramic seal. At least one conductive pathway is hermetically sealed to and disposed through the insulator body in non-conductive relationship with the ferrule. A feedthrough capacitor includes at least one active and ground electrode plate disposed within a capacitor dielectric and electrically connected to a capacitor active metallization and a capacitor ground metallization, respectively. At least a first edge of the feedthrough capacitor extends beyond a first outermost edge of the ferrule. At least a second edge of the feedthrough capacitor does not extend beyond a second outermost edge of the ferrule, or said differently, the second edge is either aligned with or setback from the second outermost edge of the ferrule.

Abstract: A filter feedthrough for an AIMD includes ferrule with an insulator hermetically sealing a ferrule opening, both cooperatively separating a body fluid side from a device side. A first conductive pathway is hermetically sealed to and disposed through the insulator. A feedthrough capacitor is disposed on the device side and includes at least one active electrode plate disposed parallel and spaced from at least one ground electrode plate within a capacitor dielectric. A capacitor active metallization is electrically connected to the active electrode plate and is in non-electrically conductive relation with the ground electrode plate. A capacitor ground metallization is electrically connected to the ground electrode plate and is in non-electrically conductive relation with the active electrode plate. An anisotropic conductive layer is disposed on the device side. The anisotropic conductive layer electrically connects the capacitor active metallization to the first conductive pathway.

Abstract: A stimulation system stimulates anatomical targets in a patient for treatment of dry eye. The system may include a controller and a microstimulator. The controller may be implemented externally to or internally within the microstimulator. The components of the controller and microstimulator may be implemented in a single unit or in separate devices. When implemented separately, the controller and microstimulator may communicate wirelessly or via a wired connection. The microstimulator may generate pulses from a controller signal and apply the signal via one or more electrodes to an anatomical target. The microstimulator may not have any intelligence or logic to shape or modify a signal. The microstimulator may be a passive device configured to generate a pulse based on a signal received from the controller. The microstimulator may shape or modify a signal. Waveforms having different frequency, amplitude and period characteristics may stimulate different anatomical targets in a patient.

Abstract: Generally discussed herein are systems, devices, and methods for providing a therapy (e.g., stimulation) and/or data signal using an implantable device. Systems, devices and methods for interacting with (e.g., communicating with, receiving power from) an external device are also provided.

Abstract: A cranial prosthesis for implanting over a portion of a patient's skull includes a body having a first major surface configured for positioning against the patient's skull; a second major surface opposite to the first major surface and forming a contour along which the patient's scalp is disposed against; and an outer perimeter defining a boundary between the first and second major surfaces. A cavity is defined along a portion of the first major surface and is configured for receiving and covering a portion of a medical device extending outwardly from the patient's skull. A tapered region extends radially outward along the body toward the outer perimeter and tapers the contour of the second major surface to reduce visibility of bulging along the patient's scalp caused by the portion of a medical device extending outwardly from the patient's skull when the prosthesis is disposed over the implanted medical device.

Abstract: A method and system for bone regeneration is provided that includes an electrical stimulation system for the purpose of accelerating the process of bone healing. The electrical stimulation system includes a coil and a capacitor such that when the coil is powered a pulsed electromagnetic field is generated to accelerate healing. There are also implantable medical devices that include inserts such as an elbow insert. The elbow insert includes or is formed with a repeater coil and a device capacitor, such that when the coil is powered the device coil is powered and delivers a repeater pulsed electromagnetic filed to the surrounding bone. This inductive coupling provides for treatment by both the coil and the repeater coil to accelerate bone healing. The insert may be embodied so it can be used in connection with a plurality of different implantable medical devices.

Abstract: The present invention relates to a treatment apparatus using high frequency waves, and to a method for controlling same. The treatment apparatus using high frequency waves comprises: a high frequency wave generating unit; a plurality of needles for providing, into the skin of a user, high frequency energy transferred from the high frequency wave generating unit; and a driving unit for inserting the plurality of needles into the skin of the user, wherein the apparatus further comprises a control unit for controlling the driving unit such that the plurality of needles are inserted into a first target point within the skin and then move to a second target point.

Abstract: The invention relates to an electromedical implantable or extracorporeally applicable device for treating and monitoring organs as well as a method for therapeutic organ treatment. The aim of the invention is to create an electromedical implantable or externally applicable device which allows healing processes to be excited in diseased organs. Said aim is achieved by an electromedical implantable or extracorporeally applicable device for treating and monitoring organs, comprising a programmable generator and receiver unit which generates and receives electrical microcurrents and electromagnetic power and is connected in a conducting manner to electrodes, a telemetry unit that is integrated into the generator and receiver unit and is provided with a transmitter and a receiver for exchanging data with extracorporeal devices, and a power supply unit.

Abstract: This application relates to a Magnetic Stimulation (MS) and preferably Transcranial Magnetic Stimulation (TMS) system. Examples according to this disclosure provide a simple, low cost and reliable system for appropriately positioning an MS coil arrangement into a treatment position or a position for diagnosis.

Abstract: The embodiments of the present application disclose a wearable apparatus, a method for manufacturing the same, and a wearable device. The wearable apparatus may include a flexible Organic Light Emitting Diode (OLED) device including a first light-emitting layer having a first peak emission wavelength and a second light-emitting layer stacked on the first light-emitting layer, wherein the second light-emitting layer has a second peak emission wavelength which is different from the first peak emission wavelength; and a controller connected to the flexible OLED device to control an operation of the flexible OLED device.

Abstract: The present invention concerns a medical device (10) intended to be worn by a human wearer, the medical device (10) defining a first area (26) and a second area (28), each area being intended to be positioned in front of a respective eye of the wearer. The medical device (10) comprises a frame (10), comprising a rear shell (34). The rear shell (34) defines a hole (54) facing the first area (26) and the rear shell (34) is opaque facing the second area (28). The medical device (10) also comprises an optical module (20) in the first area (26). The optical module (20) comprises a light source (70) and an optical system (72). The optical module (20) is arranged to send a light beam through the hole (54). The medical device (10) further comprises an electronic circuitry (18), adapted to command the optical module (20).

Abstract: A robustness optimization is disclosed for a broad beam proton therapy plan. A nominal dose distribution (62) is computed, to be delivered to a volume by performing proton therapy on the volume according to a proton therapy plan (50) having parameters (52) defining a range compensator shape and a range band. The parameters of the proton therapy plan are adjusted to reduce a difference between the nominal dose distribution (62) and a perturbed dose distribution calculated to be delivered to the volume modified by an error scenario (64) by performing proton therapy on the volume modified by the error scenario in accordance with the proton therapy plan with the parameters adjusted by the adjusting operation. The adjusting may be repeated serially for each error scenario of a set of error scenarios (44) to produce a proton therapy plan that is robust for any of these error scenarios.

Abstract: In a method for acquiring magnetic resonance raw data for image-guided radiotherapy, a number of imaging goals are provided to a computer. For each imaging goal, a magnetic resonance imaging protocol is selected. For each selected magnetic resonance imaging protocol, a number of parameters for that protocol are adjusted according to the respective imaging goal. The resonance raw data are acquired with the magnetic resonance imaging protocol and their parameters.

Abstract: Patient's cranial position monitoring and controlling device for controlling an MR-guided radiation source module via a MR-guided radiation controlling device to be connected to the patient's cranial position monitoring and controlling device and a MR-guided radiation system comprising a patient's cranial position monitoring and controlling device, which allows for a better MR-imaging while allowing a patient position monitoring close to the patient.

Abstract: Disclosed is a method for determining a deviation of the position of an anatomical body part relative to a predetermined position defined by a radiation treatment plan. A monitoring image is taken of the anatomical body part at the instant that a predetermined control point defined in the treatment plan has been reached. The monitoring image is compared to a simulated image simulated from a planning image of the anatomical body from the perspective of a monitoring camera used to generate the monitoring image. The comparison allows for a determination of whether there is a positional deviation.

Abstract: A radiation monitor 1 includes a light-emitting unit 10 which generates light having an intensity depending on an amount of an incident radiation, an optical fiber 20 which sends a photon generated by the light-emitting unit 10, a photoelectric converter 30 which transmits one electric pulse to one sent photon, a dose calculation device 40 which counts the electric pulse amplified by the photoelectric converter 30 and converts the counted value of the measured electric pulses into a dose of the radiation, and a display device 50. The dose calculation device 40 counts the electric signals converted from the photon by the photoelectric converter 30 to calculate a counting rate, and stops the counting when the counting rate exceeds a predetermined threshold, and performs counting when the counting rate is less than the threshold.

Abstract: The present disclosure generally relates to a cystic applicator for radiotherapy and a method for determining a thickness of a scattering foil and modulator therein. According to one embodiment, a cystic applicator for radiotherapy may comprise a housing having a hollow cystic structure with an opening, a scattering foil disposed at an opening of the hollow cystic structure and configured to receive first radiation and convert a portion of the first radiation into second radiation while scattering the first radiation, and a modulator disposed inside the hollow cystic structure and configured to modulate an intensity of mixed radiation including the first radiation and the second radiation.

Abstract: The ultrasonic surgical device includes a power source configured to generate power, an ultrasonic transducer having a first resonant frequency, the ultrasonic transducer electrically coupled to the power source and configured to generate ultrasonic motion in response to the generated power, an ultrasonic probe configured to be mechanically couplable to the ultrasonic transducer, the ultrasonic transducer and the ultrasonic probe having a second resonant frequency when the ultrasonic probe is coupled to the ultrasonic transducer, and a controller configured to determine whether the ultrasonic probe is properly coupled to the ultrasonic transducer based on the first resonant frequency and the second resonant frequency.

Abstract: A surgical apparatus comprises a body, a shaft assembly, and an end effector. The end effector comprises a clamp arm and an ultrasonic blade in acoustic communication with an ultrasonic transducer via an acoustic waveguide that extends through the shaft assembly. The clamp arm is configured to pivot about a first pivot point toward and away from the ultrasonic blade along a first angular path from a first position to a second position to thereby provide a tissue sealing mode of operation. The clamp arm is further configured to pivot about a second pivot point toward and away from the ultrasonic blade along second angular path from the second position to a third position to thereby provide a tissue cutting and sealing mode of operation. The second pivot point is proximal to the first pivot point.

Abstract: The present disclosure is directed to a precision ultrasound scanner for imaging, for example, the prostate in a way that produces a superior image of the prostate while removing the iatrogenic risk and patient discomfort associated with other methods of providing an ultrasound image of the prostate. The present disclosure describes an apparatus and method for forming a high precision image of the prostate from outside the patient's body wherein the resolution in sufficient to image, for example, cancerous lesions on the surface of the prostate. To achieve such images, coded excitation, tissue harmonic imaging, advanced transducers operating in the 10 MHz to 40 MHz range is used to achieve a useable signal-to-noise reflection while being able to position the imaging transducer as close as possible to the prostate without risk or discomfort to the patient.

Abstract: A sunscreen composition comprised of one or more sunscreen active agents encapsulated in a cellulose derived capsule wherein the composition can contain one or more additional agents. A sunscreen composition can be mixed with a body wash, an after shower body lotion, a shampoo, a conditioner, a soap, a gel, a hand sanitizer, a cream, a spray, a mouse, a lotion, an ointment, a make-up product, a lip balm, a hair spray product, an arachnid/insect repellent or a medicinal product.

Abstract: A nose clip structure comprises a nose frame and nose pads. The nose frame includes two arms and a connecting portion. The connecting portion interconnects the two arms to make the two arms bend flexibly. The nose pads are disposed on the two arms of the nose frame, and has an anti-off body adapted to engage with the wing of the swimmer's nose for preventing falling-off of the nose clip structure.

Abstract: A breathing equipment training device and a method for breathing training using a breathing equipment training device. The breathing equipment training device includes a shell and a diaphragm. The shell includes a first opening and a second opening, the first opening configured to be inserted into a breathing opening in a mask to form a connection with the breathing opening of the mask, and the second opening configured to be exposed to ambient air. The diaphragm is positioned in an inner cavity of the shell about the second opening, and configured to impede airflow into the shell through the second opening.

Abstract: A breathing half mask (1) for protection against particles, aerosols and odors, having two or more mask sections (10). The breathing half mask (1) can be brought from a storage state into a use state by at least one folding process.

Abstract: A device that can be used to insert a probe into a filtering facepiece for fit testing. The device preferably includes a holder for the probe; a handle to apply force directly or indirectly to the probe; magnets that assist with alignment of the holder and the handle during a process of inserting the probe into the filtering facepiece; and a spring that facilitates separation of the holder and the handle after insertion of the probe into the filtering facepiece. The holder may further include a puncturing device to facilitate insertion of the probe. The holder and the handle preferably are separate elements positioned opposite each other to apply force to the probe. In some aspects, the holder includes a piston for driving the probe into the filtering facepiece. The spring may surround the piston. The handle preferably includes a recess capable of holding a fastener for the probe. The magnet(s) may be of any shape and type, but preferably are torus shaped neodymium magnets. Also, associated techniques.

Abstract: A fire suppression system, a method for deploying the fire suppression system, an adapter for use in the fire suppression system and a method for increasing local humidity using the fire suppression system, as well as uses of the adapter for transferring water to vehicles or aircraft are described. The fire suppression system is formed of segments of water transfer conduit extending from a main water source. The system includes a plurality of connections between at least some of the segments of water transfer conduit made using an adapter placed at a fixed location. In the system. the adapter has a main water dispensing device mounted thereon. The main water dispensing device is in water transfer communication with the water transfer conduit and the adapter includes one or more connection points for transfer of water via branch conduits extending outward from the adapter or inward to the adapter from a secondary water source.

Abstract: An integrated fire suppression system receives inert gas from onboard gas generators and water effluent from onboard water generators. The inert gas and water effluent are mixed in a gas-water mixer to generate an inert aerosol. The inert aerosol is provided to a fire suppressant distribution network and sprayed into areas of the aircraft requiring fire suppression to provide cooling and to prevent reignition.

Abstract: A firestop system for fire stopping a bus duct that passes through an opening in a marine deck or a marine bulkhead includes a boot seal wrapped around the bus duct housing. The boot seal has a top end attached to the bus duct, and a bottom end attached to the division. The boot seal is made of flexible material to allow for movement of the bus duct relative to the division due to vibration. The boot seal may be made of a thermal barrier wrap or other high-temperature insulating mat materials to allow heat generated under normal condition to escape while providing firestopping and temperature resistance under fire exposure conditions. The firestop system may also have a gasket positioned between the bus duct and the boot seal to accommodate irregularities in the outside surface of the bus duct housing.

Abstract: A fire suppression system may include a tank and a manifold in the tank. The tank, when charged, holds a liquid pressurized with a gas. The manifold has an inlet coupled to receive a liquid flow from a lower portion of the tank and inlets configured to receive gas flows from a upper portion of the tank. An expansion chamber in the manifold receives the liquid flow and the gas flows, which create a liquid-gas vortex that produces foam.

Abstract: A device for dispensing a pressurized material, includes a body defining a pressurizing chamber containing a gas generator, and a tank containing the material to be dispensed, the tank being defined by an end wall having an outlet orifice. The device includes a piston, to move inside the body, separating the pressurizing chamber from the tank, the gas generator to trigger the dispensing of the material to the outside of the body through the outlet orifice by causing the piston to pass from a material-storage, first position to an end-of-material-dispensing, second position in which the piston faces the end wall. The piston, when in the first position, presents a housing that is closed by a fragile portion beside the pressurizing chamber and that is open beside the tank, the housing containing a striker element that is held in the housing and that defines a channel opening out into the tank.

Abstract: A fire suppression agent includes a non-aqueous pressurized fluid medium and vermiculite particles suspended in the fluid medium. The fire suppression agent is capable of suppressing a fire including a combustible metal material.

Abstract: A fire suppression agent includes a fluid medium, vermiculite particles suspended in the fluid medium, and a colorant additive proximate at least a subset of the vermiculite particles. The fire suppression agent is capable of suppressing a fire comprising a combustible metal material.

Abstract: An inert gas-generating fire suppression composition is disclosed, consisting essentially of an oxidizer, comprising ammonium dinitramide and strontium nitrate, a fuel, comprising potassium isocyanurate, a gas-generate fuel, comprising guanidine nitrate and a quantity of carbon black.

Abstract: In one embodiment, an apparatus may include a first receiver and a second receiver, wherein the first receiver's first end is substantially cylindrical and wherein the first receiver's second end includes a first clamp, wherein the second receiver's first end is substantially cylindrical and wherein the second receiver's second end includes a second clamp, wherein the first receiver and the second receiver are detachably attached to one another via one or more first securing objects positioned on the first clamp and on the second clamp, and wherein at least one tightening clamp resides on the first receiver's first end and on the second receiver's first end.

Abstract: A weight bench tilt locking mechanism system and apparatus is provided. The tilt locking mechanism allows a single lever to simultaneously release two pins which are temporarily secured to two respective movable support bars which hold the bench portion of the weight bench in place. The tilt locking mechanism allows the bench to be selectively secured at various angles so as to allow a user to work out various muscles of his/her body. The tilt locking mechanism further allows the weight bench to be folded in a compact manner for storage while the device is not in use.

Abstract: A portable exercise device designed to efficiently and safely exercise the gluteal, hamstring and calf muscles. The exercise device is an inclined platform with an elongated resistance band attached to both sides of the upper surface of the inclined platform, providing resistance from the sides of the platform. An additional raised support is provided on the inclined platform, as well as resistance originating from within the platform, which optimizes the concentric and eccentric phase of every squat and lunge for maximal strength and hypertrophy of the muscles. The combination of the inclined platform with resistance from the sides and from the platform itself allows the user to conduct a variety of exercises for strengthening the muscles of the lower body.

Abstract: A treadmill folding device having a locking function includes a treadmill deck, a first upright pole, a control panel and a first lockable telescopic mechanism. The control panel is mounted to an upper end of the first upright pole. A lower end of the first upright pole is movably connected to a side of the treadmill deck. The first lockable telescopic mechanism is connected between a middle portion of the first upright pole and the side of the treadmill deck. The first upright pole, the treadmill deck and the first lockable telescopic mechanism form a triangular area when the first lockable telescopic mechanism is in an extended state. The first upright pole is parallel to or about parallel to the treadmill deck when the first lockable telescopic mechanism is in a retracted state.

Abstract: An exercise device is described. An exercise device including a body, the body having a top, a bottom, a first end located at one edge of the body, a second end located at an opposite end of the body, and first and second sides extending between the first and second ends; a first axle connected to a first wheel, the first axle also connected to the body proximate the first end at a first hub; a first spring having a first spring end, the first spring positioned at least partially within the first axle, with the first spring end slidably connected to one of the first wheel and the first hub at a first junction, wherein the first junction is configured to convey torque between the one of the first hub and the first wheel and the first spring end.

Abstract: The current invention is a Bilateral Brain Coordination Activity System requiring simultaneous performance of a set of tasks assigned to two or more extremities, e.g. hand, finger and foot. The purpose of this invention is to enhance coordination between left and right brain. The set of tasks consist of symmetric or asymmetric differentiated motions, wherein each motion requiring a distinct brain command, and therefore bilateral brain coordination. The system employs a mechanical and/or interactive digital platform with handheld or stationary devices, or rideable equipment. Difficulty level varies with the selected set of tasks, their spatial and planar arrangement and the number of involved extremities. This invention is appropriate for all ages to improve bilateral coordination and motor skill, and can be for individual use, sportsman and military training, identification of motor skill deficits, therapeutic development of compromised motor skill, and/or entertainment or game use.

Abstract: A breathing device includes a mouthpiece having a passage therein and a housing connected to the mouthpiece. The passage is configured to receive breaths including inhales and exhales. The breathing device further includes light emitters, a sensor and a controller. The light emitters have an operational status and non-operational status. The sensor is configured to sense pressure generated by the breaths and obtain pressure data associated therewith. The controller is configured to receive the pressure data and determine if breaths are exhales or inhales. The controller is further configured to transmit an inhale signal to the light emitters during an inhale to change their status in an inhale lighting predetermined sequence and timing. The controller is also configured to transmit an exhale signal to the lights emitters during an exhale to change their status in an exhale lighting predetermined sequence and timing.

Abstract: An incentive spirometer is disclosed having a helical tube, wherein the helical tube includes a first inlet, second outlet, third outlet, and fourth outlet. The spirometer further includes a chamber, wherein the chamber is in fluid communication with the first inlet, second outlet, third outlet, and fourth outlet of the helical tube; and an object disposed within the spirometer, wherein the object is adapted to move through the first inlet of the helical tube and through either the second outlet, third outlet, or fourth outlet. In addition, the spirometer further includes an inhalation draw tube in fluid communication with the chamber and helical tube.

Abstract: The disclosure provides methods and systems for verifying exercise data of a user. The method may include acquiring a post containing exercise data about an exercise regimen performed by a user. The method may also include transmitting a request to a verification device for a verification result for the post and receiving from the verification device, a set of data containing a result of the verification process for the post. The method may further include causing the user devices to display the post and/or the verification results. This disclosure provides a centralized platform to showcase and track the progress of the exercise regimen performed by the user and by other users who are followed by the user.

Abstract: An exercise device in accordance with the present disclosure may include a body having a first end and a second end, wherein a first end is configured to receive a handle attachment. The exercise device may also include a first connection component disposed at the second end of the body and configured to attach the exercise device to a first resistance component. A sensor may be coupled to the first connection component. Additionally, a processing circuit may be disposed in the body of the exercise device communicatively coupled to the sensor. The exercise device may include a rotatable display configured to be visible to a user as a user performs movements with the exercise device.

Abstract: Example embodiments relate to systems, methods, apparatuses, and computer readable media relating to a user interface, that may for example, receive and/or process physical activity data and allow interaction with the received information in novel implementations.

Abstract: Systems and methods are for production, management, syndication and distribution of digital assets through a network such as the Internet or wireless network. Digital media assets are distributed to consumers through a syndicated network of Outlets under control of a central platform. Distribution is format agnostic. There is a single platform between the B2B2C, wherein a platform allows, through a single access for each stakeholder, the ability to each have control over availability dates and pricing specifications to a plurality of merchants and/or subscription outlets or channels. Subscription channels can support micro-subscriptions with diversely curated and priced offerings, including acceptance of crypto-currency. The delivered media assets may include content associated with an exercise apparatus, including content for an exercise session including computer generated content and computer augmented content created in response to exercise session data.

Abstract: Systems and methods are for production, management, syndication and distribution of exercise class content for use with an exercise apparatus. An exercise content distribution system includes a database storing the exercise content and data associated with a content provider and an application provider, and a platform server operable to facilitate delivery of the exercise content to the exercise apparatus. The platform server is configured to deliver archived exercise classes, receive a selection of one of the archived exercise classes, transmit data representing content of the selected archived exercise class, receive performance data based on activity by the first user, generate archived performance data for a plurality of other users, and dynamically update a ranked list and at least some of the synchronized archived user performance parameters for display by the exercise apparatus.