An inflatable massage shoe includes a sole, a vamp installed on the sole, and an inflatable massage device having a main airbag and a massage airbag connected to the main airbag. The main airbag is installed on the sole and has an elastic device installed in the main airbag; the massage airbag is installed on an inner side of the vamp and communicated with the main airbag through a pipeline, and a gas in the main airbag can be exchanged with the gas in the massage airbag through the pipeline; and the vamp further includes a protective shell and an inner lining, and the massage airbag is installed between the protective shell and the inner lining. This inflatable massage shoe provides active massage actions, simulates the massage effect, and improves the comfortability, practicality, and promotion of massage shoes.

Embodiments include systems, methods, and products for prevention and treatment of orthostatic hypotension, edema, and nocturia. Aspects include a tubular compression sleeve having an adjustable effective radius. Aspects also include a position sensor. Aspects also include an actuator in communication with the position sensor, wherein the actuator is capable of modifying the effective radius of the tubular compression sleeve.

Systems, and methods relate to a medical device receiving a treatment parameter operating point within a first operating region defined by a first set of operating points for which automatic incremental adjustment of a parameter in the current operation is permitted. In an illustrative example, incremental adjustment may use artificial intelligence based on patient feedback and sensor measurement of outcomes. Some exemplary devices may receive a request to alter the current treatment parameter operating point to a second treatment parameter operating point outside the first operating region and in a second operating region in a known safe operation zone, bounded by a known unsafe zone unavailable to the user. In the second operating region, some examples may restrict the step size of incremental adjustments requested by the user. Data may be collected for cloud-based analysis, for example, to facilitate discovery of more effective treatment protocols.

An inflatable belt 100 for use in a BFR system with an outer belt material 102 hermetically sealed to an inner belt material 101 along a perimeter, thereby forming at least one inflatable chamber 103, the inflatable chamber having an input port 104 for accepting a gas into the chamber, the inflatable belt further comprising a first fastening means 110 in communication with the outer belt material, for attaching to a second fastening means 111 in communication with the outer belt material, thereby locking a circumference of the inflatable belt, when wrapped around a user's limb, efficacy feedback means 200 for gathering efficacy feedback data 205, for use in prescribing, monitoring and adjusting one or more training parameters of a BFR training session and/or program based on evaluation of the efficacy feedback data.

Systems, and methods relate to a medical device receiving a treatment parameter operating point within a first operating region defined by a first set of operating points for which automatic incremental adjustment of a parameter in the current operation is permitted. In an illustrative example, incremental adjustment may use artificial intelligence based on patient feedback and sensor measurement of outcomes. Some exemplary devices may receive a request to alter the current treatment parameter operating point to a second treatment parameter operating point outside the first operating region and in a second operating region in a known safe operation zone, bounded by a known unsafe zone unavailable to the user. In the second operating region, some examples may restrict the step size of incremental adjustments requested by the user. Data may be collected for cloud-based analysis, for example, to facilitate discovery of more effective treatment protocols.

Improved systems and methods for performing external counterpulsation (ECP) treatment are described. The system can be more compact and portable than conventional devices and, in some cases, can be incorporated into a pair of pants or a jumpsuit, such that the user can remain ambulatory during treatment. In various instances, the ECP techniques can include applying complex pulse sequences and treating conditions including cognitive disorders, diabetes, and renal disease, among others. The various techniques can also be used in emergency cardiac situations. The techniques can also be used to provide users with the benefits of exercise, without needing to experience the strain and difficulty associated with conventional cardiovascular exercise routines.

A device can comprise: a trigger chamber, having a trigger elastic wall and a trigger base wall, the trigger chamber configured for relative motion between the trigger elastic wall and the trigger base wall; a connecting line fluidly coupled to the trigger chamber, the connecting line having a substantially inelastic wall; a stimulation chamber fluidly coupled to the connecting line, the stimulation chamber having a stimulation elastic wall and a stimulation base wall, the stimulation chamber configured for relative motion between the stimulation elastic wall and the stimulation base wall, the stimulation elastic wall having an exterior surface; a plurality of projections coupled to the exterior surface; and a stabilizing frame, the stabilizing frame having a substantially rigid wall, the stabilizing frame having a plurality of apertures, the stabilizing frame extending over the stimulation chamber, the projections configured to extend through the apertures when the stimulation chamber is expanded.

An apparatus for applying periodic pressure to the limb of a patient to prevent deep vein thrombosis and pulmonary embolism. The apparatus has a cuff that has a bladder. A housing that is attached to the cuff. A pump for inflating the bladder to a maximum cuff pressure, the maximum cuff pressure being 55 mmHg, and the pump is housed within the housing. A plurality of pressure application modes each of which control operation of the pump and wherein each pressure application mode is progressively applied in a manner that will increase a patient's blood flow. A pressure application mode selector is disposed on the housing. A microprocessor that is equipped with a program that controls the pump and the plurality of pressure application modes. The microprocessor is housed within the housing and it is connected to a transceiver. And, a remote that connects to the transceiver.

A massage device includes a rotatable member rotatably supported on a supporting base with a pivot axle, and a neck massage member engaged onto the rotatable member and rotated in concert with the rotatable member relative to the supporting base for engaging with a neck portion of a user and for exercising and massaging the neck portion of the user. The supporting base includes a number of rollers engaged with the rotatable member for rotatably supporting the rotatable member on the supporting base. The supporting base includes a number of sockets for engaging with and for supporting the rollers.

A fluid-driven actuator 100 is disclosed herein. In a specific embodiment, the fluid-driven actuator 100 comprises a bending actuator 200 including a first wall portion 201, a second wall portion 203 cooperating with the first wall portion 201 to define an undulating actuator profile. The bending actuator 200 also includes an inner fluid bladder 202 disposed between the first and second wall portions 201,203 and following the undulating actuator profile. The fluid-driven actuator 100 further comprises a restraint member 300 arranged to cooperate with the bending actuator 200 to produce a plurality of motions in response to fluid supplied to the inner fluid bladder 202. Methods of producing the fluid-driven actuator are also disclosed.