Wearable sensors that measure one or more parameters such as pressure, force, acceleration, or skin temperature, are used to measure, record, display and monitor the efficacy of therapeutic maneuvers applied to a subject by an operator. Systems and methods for assessing the physiological efficacy of therapeutic maneuvers performed by an operator on a subject in need thereof, and provide a way to guide subsequent therapeutic maneuvers toward optimal outcome. In some embodiments, the systems and methods measure, record, and display physiological parameters of an operator and/or subject during application of cardiopulmonary resuscitation (CPR).

A computer-implemented system may include a treatment device configured to be manipulated by a user while the user is performing a treatment plan, a patient interface comprising an output device configured to present telemedicine information associated with a telemedicine session, and a first computing device configured to: receive treatment data pertaining to the user while the user uses the treatment device to perform the treatment plan; identify at least one aspect of the at least one measurement pertaining to the user associated with a first treatment device mode of the treatment device; determine whether the at least one aspect of the measurement correlates with a secondary condition of the user; and, in response to a determination that the at least one aspect of the at least one measurement is correlated with the at least one secondary condition of the user, generate secondary condition information indicating at least the secondary condition.

A distension/compression device for assisting breathing in a subject is disclosed. In one embodiment, a first tube includes a flexible and elastic material that forms a first tube lumen extending from a proximal end to a distal end of the first tube. Longitudinal expansion of the first tube is restricted less than radial expansion of the first tube. A connection element including a first air supply port is in fluid communication with an open proximal end of the first tube lumen and attached to a proximal end of the first tube. A method for assisting breathing of a patient and a method for assisting the clearing of secretions is also included.

A gait training system has a motor connected to a first linkage system by an actuator. The first linkage system has multiple linkage members connected to multiple joints and an endpoint that is configured to produce a cyclic gait motion when the motor is activated. First and second linkage members have an adjustable length. A method of customizing a gait pattern on a gait training system is also described.

A computer-implemented system may include a treatment device configured to be manipulated by a user while the user is performing a treatment plan, a patient interface. and a computing device configured to: receive treatment data pertaining to the user who uses the treatment device to perform the treatment plan; identify at least one enhanced component using the treatment data; generate an enhanced environment using the at least one enhanced component and the treatment plan; output at least one aspect of the enhanced environment to at least one of the patient interface and another interface; receive subsequent treatment data pertaining to the user; and selectively modify at least one of the enhanced environment and at least one of the at least one aspect of the treatment plan and any other aspect of the treatment plan using the subsequent treatment data.

A wearable medical device comprises a garment configured to be worn about a torso of a patient. The wearable medical device further comprises a CPR sensor for detecting a characteristic of a CPR therapy provided to the patient. The CPR sensor is coupled to the garment to provide movement between a stowed position and a deployed position. The CPR sensor is positioned at a center of a chest of the patient when the CPR sensor is in the deployed position. The wearable medical device further comprises an output device. The wearable medical device further comprises a processor configured for processing information from the CPR sensor and providing, to the output device, information about the CPR therapy provided to the patient.

A resuscitation device for assisting a rescuer in resuscitating a patient. A handheld computing/communication device may be configured for performing a non-resuscitation function during time periods when resuscitation is not required, the handheld device may be further configured to provide CPR prompts during time periods when used by a rescuer to assist in resuscitation, and a sensor may be provided to measure a parameter (e.g., chest acceleration) relevant to resuscitation. A CPR-assistance element may be configured to be applied to the patient and to communicate with the handheld computing/communication device.

A medical device system for providing sensor data capture includes a medical device that may include one or more removably coupled sensor hubs and that includes a display to provide sensor data and at least one data interface (DI) port that may be a sensor-agnostic DI (SA-DI) port and a data transfer cable that may be compatible with the sensor-agnostic DI port and includes a first electromechanical connector configured to detachably couple to the SA-DI port and a second electromechanical connector configured to couple to the sensor and that includes a cable memory and processor configured to execute stored software to format sensor data according to a protocol of the SA-DI port, an authentication circuit, and a cable isolation device to limit patient leakage current flow from the medical device to the sensor and to electrically isolate the authentication circuit from the cable processor and the cable memory.

A system for automated delivery and monitoring compliance for repeated remote ischemic conditioning treatments incudes at least one device for automated delivery of the therapy and at least one communications module to collect and record usage data. Reports of subject compliance with a predetermined schedule of therapy delivery is transmitted to the central database and a prescribing physician.

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.