A system and method for optimizing a patient's Kegel exercises is provided. The system includes a user interface device and a vaginal device. The vaginal device includes an intra-vaginal probe having an accelerometer that is configured to generate a signal in response to movement of the probe. The user interface device is connected to the vaginal device and analyzes signals from the accelerometer to provide physiological feedback information to the patient. The vaginal device may be connected to the user interface device via wireless communications such as BLUETOOTH® or by wire. The user interface device may be a smart device or a computer that transmits information to central web-based data server accessible by the patient or authorized healthcare providers or third-party payers.

The present invention relates to intravaginal devices, systems including the devices, and methods of using the devices to train an individual in the performance of exercises (e.g., pelvic floor lifts (PFLs) and pelvic floor relaxations (PFRs)) that strengthen the individual's pelvic floor muscles in order to treat or prevent pelvic floor disorders (e.g., pelvic organ prolapse and incontinence) and their accompanying symptoms.

A computer-implemented method for pelvic floor feedback. The method includes capturing a strength of action potentials via wireless sensors, the wireless sensors positioned proximate to a pelvic floor of a user. The method also includes transmitting the strength of the action potentials to a mobile device. The method also includes recording the strength of the action potentials on the mobile device.

For measuring functionality of an orifice (16, 20) in the human pelvic region an elongated probe (4; 54) for insertion in the orifice (16, 20) is provided. The probe (4; 54) comprises one or more electrodes (5a-6a, 5b-6b, 6a-7a, 6b-7b; 55a-56a, 55b-56b, 56a-57a, 56b-57b, 57a-92a, 57b-92b) for stimulating receptors (23, 25) in tissue bounding the orifice (16, 20) and one or more muscle activity sensors (8a, 8b, 8c, 9a, 9b, 9c, 10a, 10b, 10c, 10d, 11a, 11b, 11e, 12a, 12b, 12c; 58a, 58b, 58c, 59a, 59b, 59c, 60a, 60b, 60c, 60d, 61a, 61b, 61c, 62) for sensing muscle activity causing pressure to be exerted by tissue bounding the orifice (16, 20). A control system (I) connected to the probe (4; 54) is arranged for outputting a neurostimulation signal (35) to the electrode or electrodes and for registering a pressure signal or signals from the pressure sensor or sensors during a time interval directly subsequent to the outputting of the neurostimulation signal.

An apparatus for testing and exercising pelvic floor musculature, the apparatus comprising an elongate housing adapted for a pelvic floor aperture. The housing accommodates an oscillator and an accelerometer connected to a signal processor configured for communicating signals representative of values read from the accelerometer. A result is calculated from an applied oscillation and a response measured, and used for characterizing the musculature. In one embodiment the frequency resulting in the greatest response from the musculature is measured, and this frequency is applied during exercise.

A vaginal dilation device is provided that may include any of a number of features. One feature of the vaginal dilation device is that it is configured to dilate vaginal tissue during labor to prevent tissue damage. Another feature of the vaginal dilation device is that it can be manually controlled to dilate vaginal tissue, or can be automatically controlled to dilate vaginal tissue. In some embodiments, the vaginal dilation device is configured to measure a force applied by the device to tissue. In other embodiments, the vaginal dilation device is configured to apply a constant force to tissue. In other embodiments, the vaginal dilation device is configured to expand at a constant rate. Methods associated with use of the vaginal dilation device are also provided.

An apparatus for testing and exercising pelvic floor musculature, the apparatus comprising an elongate housing adapted for a pelvic floor aperture. The housing accommodates an oscillator and an accelerometer connected to a signal processor configured for communicating signals representative of values read from the accelerometer. A result is calculated from an applied oscillation and a response measured, and used for characterizing the musculature. In one embodiment the frequency resulting in the greatest response from the musculature is measured, and this frequency is applied during exercise.

A physical training system for pelvic floor muscle, wherein the physical training system for pelvic floor muscle is capable of providing at least one optional exercising setting to user for making the physical training system for pelvic floor muscle can guide the user to accomplish at least one exercising movement, wherein the exercising setting is selected from a group of exercising settings, wherein the group of exercising settings comprises an exercising movement setting, an exercising time setting, an exercising intensity setting, an exercising frequency setting, an exercising guidance setting, an exercising auxiliary setting and an exercising feedback setting, wherein the physical training system for pelvic floor muscle comprises a processor and a Client, wherein the processor is capable of providing at least one optional exercising setting to user, wherein the exercising settings are set to be displayed on the Client.

Embodiments generally relate to a device for monitoring air pressure in the body of a patient. The device comprises a tube comprising a feeding lumen; a sensor lumen positioned parallel to the feeding lumen; at least one sensor positioned in the sensor lumen; and at least one perforation positioned to expose the at least one sensor to an air pressure within the body of a patient when the device is positioned at least partially in the airway of the patient. The at least one sensor is configured to generate data related to the pressure to which the sensor has been exposed.

Various systems are disclosed herein for detecting, monitoring, evaluating, and characterizing pain. They systems include a number of connected components, such as a provider device, a body-mapping system, a patient device, a user device, a referred pain device and/or a rectal probe device. Accordingly, the systems allow providers to track location-specific pain intensity for any number of patients over time in order to generate reports and determine treatment recommendations for such patients.