Processing generated sensor data of a mobile deep vein thrombosis (DVT) device may include identifying use of the mobile DVT device corresponding to a user. Sensor data associated with the user's identified use of the mobile DVT device may be generated. At least some of the generated sensor data may comprise use data associated with a duration of use of the mobile DVT device by the user. A protocol associated with use of the mobile DVT device may be processed. The generated use data and the protocol associated with use of the mobile DVT device may be correlated. Based on correlating the generated use data and the protocol, an alert associated with the generated use data and the protocol may be generated.

Processing generated sensor data of a mobile deep vein thrombosis (DVT) device may include identifying use of the mobile DVT device corresponding to a user. Sensor data associated with the user's identified use of the mobile DVT device may be generated. At least some of the generated sensor data may comprise use data associated with a duration of use of the mobile DVT device by the user. A protocol associated with use of the mobile DVT device may be processed. The generated use data and the protocol associated with use of the mobile DVT device may be correlated. Based on correlating the generated use data and the protocol, an alert associated with the generated use data and the protocol may be generated.

A lifting belt includes a lifter configured to generate a tractive force in a longitudinal direction of a spinal column by expansion, a left connector and a right connector respectively disposed on a left side and a right side of the lifter, and a central connector attachable to or detachable from the left connector and the right connector.

A lifting belt includes a lifter configured to generate a tractive force in a longitudinal direction of a spinal column by expansion, a left connector and a right connector respectively disposed on a left side and a right side of the lifter, and a central connector attachable to or detachable from the left connector and the right connector.

The present invention provides a limb compression device, including: a main body having a first surface where a support portion wrapping around a portion of a limb is provided, and a second surface where a fixing shaft fixing a cuff wrapping around a remaining portion of the limb is mounted; a drive motor coupled to the main body; a reduction gear unit coupled to a drive shaft of the drive motor; a cuff fixing drum fixing the cuff, and having a first end coupled to the reduction gear unit and a second end coupled to the main body such that the cuff fixing drum winds and unwinds the cuff; and the cuff including a first end fixed to the cuff fixing drum and a second end wound around the fixing shaft via the support portion of the main body so as to wrap around the remaining portion of the limb.

The present invention provides a limb compression device, including: a main body having a first surface where a support portion wrapping around a portion of a limb is provided, and a second surface where a fixing shaft fixing a cuff wrapping around a remaining portion of the limb is mounted; a drive motor coupled to the main body; a reduction gear unit coupled to a drive shaft of the drive motor; a cuff fixing drum fixing the cuff, and having a first end coupled to the reduction gear unit and a second end coupled to the main body such that the cuff fixing drum winds and unwinds the cuff; and the cuff including a first end fixed to the cuff fixing drum and a second end wound around the fixing shaft via the support portion of the main body so as to wrap around the remaining portion of the limb.

A compression device particularly suited for DVT prophylaxis includes a disposable wrap and a re-usable controller removably mounted on the wrap to apply a tensioning force to the wrap when it is encircling the limb of a patient. The wrap includes an RF chip with a unique identifier and the controller includes an RF sensor and processor to authenticate the wrap before commencing a compression cycle. A kiosk is provided for storing a plurality of wraps for use by patients and a plurality of controllers to be used with any of the wraps. The processor of each controller can control an electric motor in the controller to tighten and loosen the wrap according to a three-stage DVT prophylaxis protocol that produces an optimum blood flow velocity. An accelerometer and software/firmware in the controller can also measure and summarize patient activity while wearing the device.

A compression device particularly suited for DVT prophylaxis includes a disposable wrap and a re-usable controller removably mounted on the wrap to apply a tensioning force to the wrap when it is encircling the limb of a patient. The wrap includes an RF chip with a unique identifier and the controller includes an RF sensor and processor to authenticate the wrap before commencing a compression cycle. A kiosk is provided for storing a plurality of wraps for use by patients and a plurality of controllers to be used with any of the wraps. The processor of each controller can control an electric motor in the controller to tighten and loosen the wrap according to a three-stage DVT prophylaxis protocol that produces an optimum blood flow velocity. An accelerometer and software/firmware in the controller can also measure and summarize patient activity while wearing the device.

In some embodiments, the present invention is directed to an exemplary inventive method having steps of: providing at least one housing having a pre-determined physical structure; fixing a first edge of at least one electro-active polymer (EAP) film within the at least one housing; connecting a first edge of at least one pulling mechanism to a second edge of the at least one EAP film; where a second edge of the at least one pulling mechanism extends outside of the at least one housing; sufficiently pulling at the second edge of the at least one pulling mechanism to form at least one pre-stretched EAP film that has been stretched in a first axial direction within the at least one housing by a first pre-determined, pre-stretched amount; and where the pre-determined, pre-stretched amount is limited by the pre-determined physical structure of the housing.