A system and method for voice-based control of sexual stimulation devices. In some configurations, the system and method involve receiving voice data, analyzing the voice data to detect spoken commands, and generating control signals based on the commands. In some configurations, the system and method involve receiving voice data, analyzing the voice data for non-speech vocalizations, detecting voice stress patterns, and generating control signals based on the detected patterns. In some configurations, the analyses of the voice data are performed by machine learning algorithms which may be trained on associations between speech and non-speech vocalizations of a user while the user engages in one or more voice-based training tasks, associating speech and non-speech vocalizations with controls of the sexual stimulation device. In some configurations, machine learning algorithms are used to make the associations. In some configurations, data from other biometric sensors is included in the associations.

A computer-implemented system may include an electromechanical machine configured to be manipulated by a user while the user performs a treatment plan, an interface comprising a display configured to present information associated with the treatment plan, and a processing device configured to receive, from one or more data sources, information associated with the user, wherein the information comprises one or more risk factors associated with a cardiac condition or a cardiac outcome, generate, using one or more trained machine learning models, the treatment plan for the user, wherein the treatment plan is generated based on the information associated with the user, and the treatment plan comprises one or more exercises associated with managing the one or more risk factors in order to reduce a probability of a cardiac intervention for the user, and transmit the treatment plan to cause the electromechanical machine to implement the one or more exercises.

Systems and methods are provided for controlling infrared radiation (IR) sources of a sauna including tuning IR wavelength-ranges and radiated power-levels of IR sources, and directing IR to locations on a user's body. In one illustrative embodiment, a sauna may be provided having adjustable IR emitters to emit IR at any wavelength resulting in a desirable radiation treatment for the sauna user. In another illustrative embodiment, a method is provided for tuning IR emitters in a sauna.

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 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.

Provided is a limb compression and circulation apparatus in which, due to a small and light body and a rechargeable power supply device, the limb compression and circulation apparatus is usable regardless of place while being worn and used by a user who is moving. The limb compression and circulation apparatus may include a first air hose connected to one end of an air pressurization portion to send air generated by the air pressurization portion and a plurality of second air hoses connected to the other end of the first air hose and allowing the air generated by the air pressurization portion to diverge and to blow into an air cuff so as to perform effective air divergence. The limb compression and circulation apparatus may prevent air leakage by coupling an air inlet/outlet hole of a second adaptor with an air hose to communicate with each other.

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.

A remotely controlled powered chair may include a support frame, a seat pivotally mounted on the support frame, an rotary actuator mounted between the support frame and the seat to drive the seat to move relative to the support frame, a backrest pivotally mounted on the seat, and a linear actuator mounted between the seat and the backrest to drive the backrest to move relative to the seat. Thus, the rotary actuator may be controlled by an electrically control device to drive the seat to pivot relative to the support frame reciprocally in a pendulum manner so that the seat is pivoted relative to the support frame automatically. In addition, the linear actuator may be controlled by the electrically control device to adjust the inclined angle of the backrest so as to provide a comfortable sensation to the user. A remotely controlled powered chair may include a base assembly. A chair frame is supported on the base assembly. An actuator mechanism may communicate with the base assembly and the chair frame, and is operable to actuate the chair frame between first and second positions.

Provided is a skin care device including a head part brought into contact with skin of a user, a battery configured to supply power for operation of the head part, a body part having a fastening portion provided at one end to which the head part is fastened and provided with the battery therein, and a cap assembly detachably attached to one end of the body part and forming an accommodation space configured to accommodate the head part, wherein the cap assembly includes a sterilization module disposed to irradiate ultraviolet light toward the head part when the cap assembly accommodates the head part.