The pain-relieving apparatus has a housing, a stimulating surface, user inputs, and a plurality of ports, such as a battery port and a transcutaneous electrical nerve stimulation (TENS) output connector. The stimulating surface may include a suction ring, vacuum apertures, vibration stimulators, a plate, heat and cold transducer elements, and medicinal holders to provide various approaches for relieving pain. The pain-relieving apparatus may also have a sound speaker for producing nerve stimulating sounds.

A device which utilizes low intensity extracorporeal shock therapy for purposes of treating soft tissue damage, cellulite reduction, or erectile dysfunction, to permit a simple, inexpensive, robust, home use solution which permits self-applied treatment for various parts of the user's body with a form factor, display, information, guidance, tutorials and training, marketing communication and purchase opportunities, viewing angle, timers, annunciators, sound attenuation, and payment options which provide an untrained amateur user with all tools and guidance necessary to properly, effectively, safely and affordably self-administer treatments.

A system for facilitating resuscitation includes: a first electrode assembly having a therapy side and a first motion sensor; a second electrode assembly having a therapy side and a second motion sensor; processing circuitry operatively connected to and programmed to receive and process signals from the first and second motion sensors to estimate at least one of a chest compression depth and rate during administration of chest compressions and to compare the chest compression depth or rate to a desired range; and an output device for providing instructions to a user to administer chest compressions based on the comparison of the estimated chest compression depth or rate to the desired range. One or both of the electrode assemblies may be constructed so that the conductive therapeutic portion is able to maintain substantial conformance to the anatomy of the patient when coupled thereto. For example, at least a portion of the flexible electrode pad may be able to flex from a more rigid sensor housing, or the sensor housing itself may be relatively small compared to the flexible electrode pad so as not to cause lift off of the therapeutic side from the patient.

A system to manage the sleep and/or the well-being of a passenger/user of an aircraft includes a chair to be installed in a cabin of the aircraft and interaction devices to interact with the user. The system further includes a user terminal configured to receive data relating to characteristics of a user profile of the user, and a control/command module connected to the user terminal, interaction devices and a database storing information relating to characteristics of a flight of the aircraft. The command/control module being configured to pilot the interaction devices according to the data relating to characteristics of the user profile and characteristics of the flight of the aircraft.

The invention relates to an adult choke pleasure enhancement adjustable pressure cuff device. Participants can engage in solo autoerotic asphyxiation (AEA) without accidentally suffocating to death. The adjustable cuff is inflatable and sized to encompass a participant's neck and has a timed safety release function. The participant can apply the device at default setting to fit snugly, but not impede blood flow. The participant can inflate the device to the desired level of pressure that would remain at that setting at participant's discretion. They can control what happens and for how long, as long as the participant is not incapacitated. However, if at any time, the controls/settings are not engaged by the participant, the device would automatically default to zero pressure after a set time. The use of the device therefore allows a participant to safely engage in solo AEA without risking injury or death.

A visual assistance system or distance and location detection system is provided. The system comprises a sensor detecting distance of objects in a user's path and alerting the user when an object is within a designated proximity to the user. The system further comprises a location detection system using GPS technology that tracks the user's location and issues an alert to the user or other individual when the user's location exceeds the boundaries of a designated safe zone.

A method for controlling a robotic walking assistant that includes a wheeled base having one or more wheels, two handles and a foldable seat that are coupled to the wheeled base, includes: detecting whether two hands of a user have held the two handles of the robotic walking assistant; receiving a command from the user to select an operation mode in response to detection of the two hands holding the two handles; controlling the wheeled base to move in response to a walking assistive mode being selected; providing resistance to at least one of the one or more wheels according to selection of the user, in response to a walking training mode being selected; and locking the one or more wheels in response to a static training mode being selected.

A robotic walking assistant includes a wheeled base having a base and one or more position adjustable wheels connected to the base, a body disposed in a vertical direction, positioned on the wheeled base and having a handle, and a control system that receives command instructions. Each of the one or more wheels is slidable with respect to the base between a retracted position and an extended position in a direction that is substantially parallel to a surface where the wheeled base moves. In response to the command instructions, the control system moves the one or more wheels between the retracted positions and the extended positions.

A method for optimizing at least one exercise. An exercise apparatus is configured to enable a user to perform the at least one exercise. The method includes receiving user data. The method includes generating, based on the user data, initial target data. The method includes receiving measurement data associated with one or more sensors. The method includes determining, differential data. The determining is based on one or more differences between the initial target data and the measurement data. The method includes receiving cohort data. The method includes generating, via an artificial intelligence engine and based on the differential data, a machine learning model trained to generate message data based on a difference between the differential data and the cohort data. The method includes transmitting, to an interface associated with a user, a message to the user based on the message data.

A method includes receiving treatment data associated with a user capable of using a treatment device to perform a treatment plan. The method also includes receiving alignment data associated with the user while the user engages in at least one activity and receiving at least one alignment characteristic associated with the user and determining, using at least the at least one alignment characteristic, whether the at least one alignment characteristic correlates with at least one secondary condition of the user. The method also includes generating secondary condition information indicating at least the secondary condition and modifying at least one aspect of the treatment plan in response to receiving, from a healthcare professional, treatment plan input. The treatment plan input includes at least one modification to the at least one aspect of the treatment plan and wherein, further, the treatment plan input is generated based on the secondary condition information.