Abstract: Introducer sheath (10,30,40) having a flexible kink-resistant distal tip portion (26,32,42). A multilayer sheath structure is used, with an inner tube (12) such as PTFE having a coil (14) of wire wound therearound. A first length of outer tubing (20) such as of nylon is inserted over most of the coil-wound inner tube (12) in a manner exposing a distal length of coil-wound inner tube. A second length of outer tubing (22) with a softer durometer than first outer tubing length (20), is inserted over the exposed coil-wound inner tube and extends for a slight distance beyond the end of the coil. During heat application, the outer tubing lengths (20, 22) are melted to bond to each other and to flow between the spacings of the coil turns to bond to the roughened outer surface of the inner tube (12). The distal tip region corresponding to the second tubing length is flexible and is kink-resistant due to the coil (14).

Abstract: A neuromodulation catheter includes an elongate shaft and a neuromodulation element. The shaft includes two or more first cut shapes and two or more second cut shapes along a helical path extending around a longitudinal axis of the shaft. The first cut shapes are configured to at least partially resist deformation in response to longitudinal compression and tension on the shaft and torsion on the shaft in a first circumferential direction. The second cut shapes are configured to at least partially resist deformation in response to longitudinal compression on the shaft and torsion on the shaft in both first and second opposite circumferential directions.

Abstract: A catheter assembly includes a catheter hub defining an interior cavity and a catheter tube extending distally thereof. A rigid actuator is positioned to extend proximally in the interior cavity and support a seal member positioned thereon in the interior cavity. The seal member includes a central membrane, a distal portion, and a proximal portion. An hourglass shaped actuator cavity is formed in the distal portion and receives a barbed end of the actuator. The outer surface of the seal member is in partial circumferential engagement with the catheter hub to define an air path that allows fluid communication between areas of the interior cavity distal and proximal of the seal member. The seal member may be configured for multi-use and include a biasing member that moves the seal member to force the membrane back over the actuator to close the membrane.

Abstract: An antimicrobial, securement, and position verification device for medical catheters is disclosed. A film, medical grade adhesive, and antimicrobial substance disposed on the medical grade adhesive operate in conjunction to secure the device to the patient's skin and to prevent infections. The catheter is secured by guide channels in the foundation and securement cover through the use of one or more adhesives impregnated with antimicrobial substances. The device further comprises catheter position alert media and indicators configured to indicate any unintentional positional changes.

Abstract: Disclosed is an arterial access sheath for introducing an interventional device into an artery. The arterial access sheath includes an elongated body sized and shaped to be transcervically introduced into a common carotid artery at an access location in the neck and an internal lumen in the elongated body having a proximal opening in a proximal region of the elongated body and a distal opening in a distal region of the elongated body. The internal lumen provides a passageway for introducing an interventional device into the common carotid artery when the elongated body is positioned in the common carotid artery. The elongated body has a proximal section and a distalmost section that is more flexible than the proximal section. A ratio of an entire length of the distalmost section to an overall length of the sheath body is one tenth to one half the overall length of the sheath body.

Abstract: A needle guard assembly having a resilient arm extending from a base situated to slide along the shaft of a needle. In one implementation the needle guard has an elongate containment member that rides with the resilient arm and is co-operable with the resilient arm to effectuate a covering of the entire distal tip of the needle upon the needle being refracted into the needle guard.

Abstract: A bi-directional cannula feature capture mechanism is described herein. Generally, the capture mechanism comprises an inner housing, an outer housing, and a cannula. The inner housing comprises a proximal and a distal cannula feature mating component. The outer housing is adapted to slidably receive the inner housing in a proximal direction. Additionally, the cannula extends through the inner housing and the cannula's feature has a proximal engagement and a distal engagement. The proximal and distal engagements are respectively configured to irreversibly engage the proximal and distal cannula feature mating components when the cannula tip is moved into a shielded position.

Abstract: A dilation catheter device and system for dilating an opening in a paranasal sinus and/or other passageways within the ear, nose or throat is disclosed. A dilation catheter device and system is constructed in a manner that facilitates ease of use by the operator and, in at least some cases, allows the dilation procedure to be performed by a single operator. Additionally, the dilation catheter device and system may be useable in conjunction with an endoscope and/or a fluoroscope to provide for easy manipulation and positioning of the devices and real time visualization of the entire procedure or selected portions thereof. In some embodiments, shaft markers are disposed on a shaft of the dilation catheter and have a light color to contrast with a dark color of the dilation catheter shaft. The high contrast between the markers and catheter shaft allows for easy viewing of the markers in low light and operation conditions.

Abstract: Methods and systems for a tissue expander according to various aspects of the present invention may function in conjunction with an extended tissue expander, such as an extended tissue expander to be temporarily implanted into a patient to form a pocket for a permanent implant. Systems and methods according to various aspects of the present invention may comprise an extended tissue expander configured to increase and/or customize the size and/or shape of a tissue pocket beyond the size and/or shape provided by a conventional tissue expander. The extended tissue expander may comprise a tissue expander coupled to an extension portion. In one embodiment, the extended tissue expander may preserve a breast pocket with a desired teardrop shape that does not need extensive surgical modification before placement of a final breast implant or a tissue flap.

Abstract: A silicone adhesive composition including an ionic silicone and useful for healthcare applications such as wound care and drug delivery.

Abstract: Embodiments provide apparatus and methods for producing markings in the skin. One embodiment provides an apparatus for marking the skin comprising a housing and reservoir for storing a skin colorant. An electrode is positioned within the housing so as to be electrically coupled to the colorant in the reservoir and is configured to be coupled to a current source and return electrode. A colorant applicator having at least one fluid pathway is coupled to a housing distal end. The applicator proximal end is positioned such that the fluid pathway is coupled with the reservoir. The applicator distal end applies colorant to the skin surface through the fluid pathway as the applicator is moved across the skin. The electrode delivers current from the current source to the skin to transport charged pigment elements of the colorant into the skin using an electromotive driving force to produce a marking in the skin.

Abstract: A protective cap having a first cap and a second cap that are removably coupled together for use in short-term and long-term antimicrobial treatment of needleless connectors and access ports of an infusion system. The instant invention further provides a protective cap having a first cap and a second cap that each coupled to a different surface of a component of an infusion system, such as a syringe. The instant invention further provides a strip containing a plurality of disposable protective caps.

Abstract: Methods for allowing a user to control a neuromodulator to modify a cognitive state being experienced by the user. The user may select a waveform ensemble from a hand-held user device having an interface, and the user may adjust the perceived intensity of the applied waveform ensemble with the user device while the waveform ensemble is being applied. Also described are methods of managing communication between the hand-held user device (such as a smartphone or the like) and a wearable neurostimulator. Methods of displaying and visually tracking and controlling the applied waveform ensemble are also described herein.

Abstract: An implantable electrical lead is provided. The electrical lead comprises an electrically insulative, flexible, elongated lead body having a proximal end and a distal end, an electrical contact carried by the distal end of the lead body, an electrical terminal carried by the proximal end of the lead body, an electrical conductor axially extending within the lead body between the electrical contact and the electrical terminal, and a stiffening tube extending within the proximal end of the lead body from a point proximal to the terminal to a point distal to the terminal and proximal to the electrode. An implantable lead assembly kit comprises the implantable electrical lead, and a connector configured for firmly receiving the proximal end of the lead body. A method of implanting the electrical lead comprises introducing the electrical lead into a patient.

Abstract: A neural interface includes a first dielectric material having at least one first opening for a first electrical conducting material, a first electrical conducting material in the first opening, and at least one first interconnection trace electrical conducting material connected to the first electrical conducting material. A stiffening shank material is located adjacent the first dielectric material, the first electrical conducting material, and the first interconnection trace electrical conducting material.

Abstract: An implantable medical lead is disclosed herein. The lead may include a body and an electrical pathway. The body may include a distal portion with an electrode and a proximal portion with a lead connector end. The electrical pathway may extend between the electrode and lead connector end and may include a coiled inductor including first and second electrically conductive filar cores. The first and second filar cores may be physically joined into a unified single piece proximal terminal on a proximal end of the coiled inductor. The first and second cores may be physically joined into a unified single piece distal terminal on a distal end of the coiled inductor. The first and second filar cores may be helically wound into a coiled portion between the proximal and distal terminals, the filar cores being electrically isolated from each other in the coiled portion.

Abstract: An implant tool and cannula facilitate the implantation of a medical device into a patient. The implant tool includes a housing that is held by a user and a needle attached to the housing. The cannula may be positioned over the needle and delivered to a target tissue within the patient. The cannula includes an electrode at a distal portion to deliver test stimulation to confirm the location of the target site or placement of the implant tool relative to the target site before removing the needle of the implant tool. In this manner, the cannula may be repositioned within the patient until the position of the implant tool and cannula relative to the target site is verified with the test stimulation.

Abstract: Electrical energy is transcutaneously transmitted from an external charger to an implanted medical device. The external charger includes a charging head that is selectively shaped to conform to the surface of a patient to enhance charge efficiency and patient comfort. The charging head has a plurality of malleable support members extending through the charging head for affixing the flexible charging head in the selected shape, while the flexible charging head conforms to the surface of the patient. The charging head may also include one or more sensors for determining the shape of a charging coil in the charging head, which cause the charge of the coil to be adjusted based on the coil shape.

Abstract: A method and system of providing therapy to a patient implanted with an array of electrodes is provided. A train of electrical stimulation pulses is conveyed within a stimulation timing channel between a group of the electrodes to stimulate neural tissue, thereby providing continuous therapy to the patient. Electrical parameter is sensed within a sensing timing channel using at least one of the electrodes, wherein the first stimulation timing channel and sensing timing channel are coordinated, such that the electrical parameter is sensed during the conveyance of the pulse train within time slots that do not temporally overlap any active phase of the stimulation pulses.

Abstract: The present invention employed a method to control electrical activity in a target area of an animal's body by administering transcranial focal stimulation to the target area to adjust activity to normal levels. An advanced automated control system would first detect the abnormal electrical activity using tripolar concentric ring electrodes and then provides transcranial focal electrical stimulation to the target area using noninvasive tripolar concentric ring electrode system in a closed-loop continuous feedback. The automated control system would be adaptable to include the use of therapeutic drugs, either non-continuously or continuously, as a more comprehensive treatment of the abnormal electric activity.

Abstract: Devices, systems and methods are disclosed for treating a variety of diseases and disorders that are primarily or at least partially driven by an imbalance in neurotransmitters in the brain, such as asthma, COPD, depression, anxiety, epilepsy, fibromyalgia, and the like. The technology involves the use of an energy source comprising magnetic and/or electrical energy that is transmitted non-invasively to, or in close proximity to, a selected nerve to temporarily stimulate, block and/or modulate the signals in the selected nerve such that neural pathways are activated to release inhibitory neurotransmitters in the patient's brain.

Abstract: An electronic stimulator device comprises a battery, first and second output ports, and an energy discharge circuit. The energy discharge circuit is coupled to the battery and configured to receive an electrical charge from the battery and deliver the electrical charge through an energy output port. A first switch is connected between the energy output and the first output port. A second switch is connected between the second output port and electrical ground. A third switch is connected between the second output port and the energy output. A fourth switch is connected between the first output port and electrical ground. A controller comprising a processor is configured to actuate the first, second, third and fourth switches between open and close states to deliver a biphasic current pulse between the first and second output ports.

Abstract: An implantable medical device is powered by a battery to deliver one or more therapies including at least one non-life-sustaining therapy such as neural stimulation for enhancing quality of life of a patient. When the battery approaches its end of life, the implantable medical device reduces power consumption of the neural stimulation (e.g., intensity of the neural stimulation) for extending the remaining battery life while maintaining a certain amount of therapeutic benefits for the patient. In one embodiment, the intensity of the neural stimulation is reduced in a tiered manner. In one embodiment in which the implantable medical device also delivers at least one life-sustaining cardiac stimulation therapy, the neural stimulation is disabled or adjusted to reduce its power consumption (e.g., intensity) while the intensity of the cardiac stimulation therapy is maintained when the battery is near its end of life.

Abstract: System and methods for adjusting electrical therapy based on impedance changes are disclosed herein. A method in accordance with a particular embodiment includes applying a therapeutic electrical signal to a patient via an implanted portion of a patient stimulation system that includes a signal delivery device in electrical communication with a target neural population of the patient. The electrical signal is delivered in accordance with a signal delivery parameter having a first value. Using the implanted portion of the patient stimulation system, a change in an impedance of an electrical circuit that includes the signal delivery device is detected. Based at least in part on the detected impedance change, the method can further include automatically adjusting the value of the signal delivery parameter from the first value to a second value different from the first, without human intervention.

Abstract: A pacemaker programming apparatus for programming a pacemaker in an individual. The apparatus comprises means for determining the sensed-paced difference of the pacemaker in the individual: first testing means for determining the optimum AV delay while the pacemaker is atrially pacing at a raised at a heart rate; and calculation means for calculating the optimum AV delay determined by the first testing means minus the sensed-paced difference.

Abstract: A medical device system including an pacemaker implantable in a chamber of a patient's heart is configured to sense near field events from a cardiac electrical signal, establish a lower rate interval to control a rate of delivery of pacing pulses and schedule a first pacing pulse by starting a pacing escape interval set equal to the lower rate interval. The pacemaker withholds the scheduled pacing pulse in response to sensing a near-field event during the pacing escape interval and schedules a next pacing pulse to be delivered at the lower rate interval from a time that the pacing escape interval is scheduled to expire.

Abstract: A leadless pacing device (LPD) includes a motion sensor configured to generate a motion signal as a function of heart movement. The LPD is configured to analyze the motion signal within an atrial contraction detection window that begins an atrial contraction detection delay period after activation of the ventricle, and detect a contraction of an atrium of the heart based on the analysis of the motion signal within the atrial contraction detection window. If the LPD does not detect a ventricular depolarization subsequent to the atrial contraction, e.g., with an atrio-ventricular (AV) interval beginning when the atrial contraction was detected, the LPD delivers a ventricular pacing pulse.

Abstract: A method and device for updating a frequency of determining whether a lead condition is occurring in a medical device that includes sensing a cardiac signal, determining the number of days the lead has been implanted prior to implanting of the medical device, performing a first update of a virtual lead days value associated with a number of days since implant of the lead in response to the determined number of days the lead has been implanted prior to implanting of the medical device, determining whether a lead condition is occurring in response to the sensed cardiac signal, and updating a frequency of determining whether the lead condition is occurring in response to the determined first update of the virtual lead days value.

Abstract: The implantable medical device is for implantation into a patient's body and is wirelessly powered by an external control device. The implantable medical device is induced by an AC electromagnetic field of the external control device through an inductive coil. A rectifier converts the AC electromagnetic field into a DC current. A detector detects a voltage value of the DC current, and a processor produces a first piece of status information accordingly. A transceiver receives and relays the first piece of status information to the external control device so as to monitor the power consumption of the implantable medical device when it is wirelessly powered.

Abstract: An antenna for an implantable medical device (IMD) is provided that is formed on the same substrate as the telemetry circuitry for the IMD. The telemetry circuitry is formed on a portion of the substrate within the interior of a housing for the IMD, while at least one antenna is formed on an exterior portion of the substrate on the exterior of the housing to allow for far field telemetry. At least one electrical interconnect is formed on the substrate for connecting the antenna to the telemetry circuitry, where the electrical interconnect may comprise a controlled impedance line to minimize loss. A conformally-shaped hermetic cover, such as a ceramic material, may be formed in a desired shape around the exterior portion of the substrate and antenna and cofired together to form a monolithic structure encasing the antenna and exterior portion of the substrate.

Abstract: The present invention relates to a non-invasive system with diagnostic and treatment capacities that use a unified code that is intrinsic to physiological brain function. In an embodiment of the present invention, an approach to the treatment of disorders that supplements existing diagnostic and treatment methods with robust quantitative data analysis are presented. This is achieved by a unification of cognitive and neural phenomena known as the Fundamental Code Unit (FCU), representing identifiable patterns of brain activity at the submolecular, molecular, and cellular levels (intra-brain communications), as well as their manifestations in thought and language (inter-brain communications).

Abstract: The present invention relates to methods and compositions for modulating receptors in postsynaptic neurons of damaged or diseased retinas. The invention also related to methods for using the compositions set forth herein for treatment of diseases of hyperexcitability such as epilepsy.

Abstract: A photodynamic therapy lamp includes two lamp modules comprising an array of LEDs. Each of the lamp modules is movable between a first position in which an angle between the lamp modules is from 157 degrees to 180 degrees, and a second position in which the angle between the lamp modules is from 50 degrees to 70 degrees.

Abstract: A particle beam irradiation chamber in which a passage having a first opening part at a side of an inner wall and a second opening part at a side of an outer wall is provided and which has an isocenter inside the chamber, wherein a first line segment which connects the center of the first opening part and the center of the second opening part passes inside the passage, an angle, which is formed by a second segment, which connects the center of the first opening part and the isocenter and the first line segment, is smaller than 180 degrees, and a width of the passage is narrower than a width of opening of the first opening part.

Abstract: The invention relates to a therapeutic system which comprises an ultrasound therapy unit (1, 518) arranged to insonify at least a portion of a body (2, 508) of a patient with high intensity ultrasound and a MR imaging unit (3, 500) arranged to acquire MR signals from the portion of the body (2, 508) and to reconstruct a thermographic MR image from the MR signals. It is an object of the invention to enable MR guided high intensity focused ultrasound (HIFU) treatment, in which temperature values within critical anatomic regions containing fat can be monitored. The invention proposes that the therapeutic system further comprises an ultrasound diagnostic unit (5, 518) which is arranged to acquire ultrasound signals from the portion of the body (2, 508) and to derive at least one local temperature value from the ultrasound signals.

Abstract: A fitting for a fluid-circulating heat exchanging garment includes a cylindrical tube of flexible PVC extending from and integrally formed with a fluid-conducting chamber, the tube having a length, a distal portion with an inner diameter adapted to receive and closely fit a tubing end of a flexible PVC tubing, and a proximal portion with an inner diameter substantially equal to an inner diameter of the flexible PVC tubing, the cylindrical tube having a plurality of spaced apart radially-extending ribs extending the length of the tube and continuing to an outer surface of the fluid-conduction chamber. A manifold for heat exchanging garments has a central fluid-conducting chamber with a plurality of fittings extending therefrom and an inlet/outlet for connection to flexible tubing connected to a fluid circulating system.

Abstract: A vehicle-mounted fire control system for safe transport and management of a flammable liquid transported by a vehicle. The system includes a liquid storage vessel having an outer protective wall, a buffer space, and an interior wall. The outer protective wall encloses the buffer space and the interior wall. A rollover sensor measures a roll angle of the liquid storage vessel. An impact sensor measures impact acceleration of the liquid storage vessel. A smoke detector is located inside the buffer space. A fire extinguisher having a plurality of nozzles sprays fire suppressant at least onto one of the outer wall or the interior wall upon command. Electrically actuated solenoids, each one in communication with the nozzles, are configured to automatically open and spray fire suppressant upon the command. A processor programmed to issue the command upon detection of a hazard.

Abstract: A control system for a fire fighting device is provided. The control system may include a controller configured to operably connect over a network to a first valve controller controlling a status of a first valve in response to an input from the controller, a second valve controlling a status of a second valve in response to an input from the controller, and a governor operably controlling a power source in response to an input from the controller. The control system may further comprise a touchscreen display operably connected to the controller, the display configured to display the status of the first and second valves and configured to receive an input from a user, wherein controller generates a manipulatable icon displayed on the touchscreen display, a manipulation of the icon generating the input from the controller to the first valve controller.

Abstract: The present invention is a trampoline with a unique frame structure to improve strength, stability and safety. The safety poles of the trampoline are organized in a lattice type of formation with multiple joints. It provides more coverage around the trampoline as a safety mechanism. The lattice type formation also strengthens the safety poles via strategic connections, disperses force asserted onto the safety poles. As a result, the trampoline of the present invention guarantees a safe and stable amount of space for bouncing, suitable for children as well as for adults.

Abstract: A novel exercise and sporting apparatus with improved safety features is disclosed. In preferred embodiments, the apparatus comprises: a first resilient arched member having two opposite end zones, and being configured to securely engage with a foot receiving member; a second resilient arched member having two opposite end zones, and being configured to contact a ground surface; a connection element being configured to connect an end zone of the first resilient arched member with an end zone of the second resilient arched member, and a rotation-opposing assembly extending from the connection element toward a ground surface, the rotation-opposing assembly being configured to limit an amount of rotational motion of the apparatus.

Abstract: A golf ball carrying and alignment tool includes an elongated member having a generally circular aperture disposed along the bottom end. A slit traverses the bottom end and engages the aperture. A lid is hingedly secured above the aperture, a clip is disposed along the top end of the main body, and a writing instrument is removably secured within a channel on the main body.

Abstract: A sports racquet extends along an axis and is configured for use with a quantity of racquet string forming a string bed about a string plane. The racquet includes a frame formed of a thermoplastic material, and including first and second halves including first and second spaced apart hoop regions, and first and second handle regions, respectively. The hoop regions includes projections extending from hoop regions in a direction orthogonal to the string plane. At least one of the hoop regions defines a set of bores. The projections are configured to matably engage the bores. The projections extend through the string plane and define curved bearing surfaces configured for engaging and supporting the racquet string. The projections include first and second projections having first and second radii of curvature, respectively. The first radius of curvature being at least 0.5 mm greater than the second radius of curvature.

Abstract: A hollow golf club head includes a sole, a crown, a skirt, and a striking face. The golf club includes a junction interconnecting the sole, crown, and skirt to the striking face, the junction including at least one stiffening member.

Abstract: A golf club head includes a body defining an interior cavity. The body includes a sole positioned at a bottom portion of the golf club head, a crown positioned at a top portion, and a skirt positioned around a periphery between the sole and crown. The body has a forward portion and a rearward portion. The club head includes a face positioned at the forward portion of the body. In some embodiments, the crown includes a lattice-like structure having thin regions surrounded by a web of relatively thicker regions. In some embodiments, the club head includes one or more stiffening tubes attached between the sole and the crown to improve the acoustic performance of the golf club head.

Abstract: Embodiments of golf club heads and methods to manufacture golf club heads are generally described herein. In one example, a golf club head may include a body portion and a plurality of weight portions. The body portion may include a front portion, a rear portion, a toe portion, a heel portion, a top portion, a bottom portion having an outer surface associated with an outer surface curve, and a weight port region located at or proximate to the bottom portion. Other examples and embodiments may be described and claimed.

Abstract: A shaft 6 includes a plurality of fiber reinforced resin layers s1 to s10. The plurality of layers include a first straight layer s1 in which a 0°-compression strength is the minimum and a second straight layer s9 in which a 0°-compression strength is the maximum. A specific tip part Tx which is a region between a tip end Tp and a position separated by 100 mm from the tip end Tp satisfies the following (a) to (c): (a) the first straight layer forms a innermost layer; (b) the second straight layer is arranged outside a central position in a thickness direction; and (c) when a 0°-compression strength of the first straight layer is defined as Cmin and a 0°-compression strength of the second straight layer is defined as Cmax, a difference (Cmax?Cmin) is equal to or greater than 550 MPa.

Abstract: A throwing sleeve with visual biofeedback may be provided. Embodiments of the present disclosure may be comprised of a sleeve. The sleeve may be comprised of a plurality of segments forming a single, internal passageway with at least one opening. A first opening may be configured to receive an object (e.g., baseball or softball) into the internal passageway of the sleeve. A second opening may be configured to receive a user's hand. Embodiments may further comprise a means for securing the user's hand within the internal passageway of the sleeve. Still further, embodiments may comprise at least one stripe running parallel to an edge of each of the plurality of segments.

Abstract: A punching training device includes a base, a barrel, and a punching member. The base includes an upper shell and a lower shell made of soft material. The base is formed with a cavity and defines a vertical central axis wherein the cavity is located at the central axis. The lower shell has a convex cambered face at the bottom thereof. The upper shell has a connecting portion at the top thereof. The barrel has a shape corresponding to the cavity and is received in the cavity. The punching member is disposed on the connecting portion and extends upward.

Abstract: An apparatus and method for catching a golf ball is disclosed herein. More specifically, the present invention discloses a compact golf ball catching apparatus having a first energy absorbing layer located at a frontal portion of the apparatus, a second energy absorbing layer located at a rear portion of the apparatus, and a frame adapted to connect the first and second energy absorbing layer as well as provide structural integrity to the first energy absorbing layer; wherein the first energy absorbing layer slows down the speed of a golf ball as it enters and penetrates the apparatus and hinders the golf ball's ability from exiting the apparatus post impact.

Abstract: A athletic training assembly includes a base that may be positioned on a support surface. A pair of guide rods is each movably coupled to the base. Each of the pair of guide rods is curved between a first end and a second end of the pair of guide rods. The first end and the second end of each of the pair of guide rods is coupled together. The pair of guide rods forms a crescent shape. A user slidably engages an athletic implement to each of the pair of guide rods. The athletic implement travels upwardly and downwardly between the first and second ends of the pair of guide rods when the user swings the athletic implement. The pair of guide rods retains the athletic implement on a correct trajectory. The user is trained in swinging the athletic implement in the correct trajectory.