BFR DISTRAD NON OP: Blood Flow Restricted Training During Rehabilitation Following Distal Radius Fracture

Status unconfirmed · Not applicable

Conditions studied: Distal Radius Fracture, Rehabilitation

In brief

Occlusion training, resistance exercise performed with a specialized venous tourniquet, leads to beneficial changes in muscle strength at low resistance and minimal stress on the nearby joint. This novel resistance training has the potential to greatly improve muscle strength gains in individuals who are unable, for medical reasons, to perform the high resistance exercises typically required to improve strength. Our study will examine the effect of this technique on strength recovery following distal radius fracture treated with cast immobilization (non-operatively). The primary objective of the intervention is to achieve accelerated recovery of forearm, wrist and hand function as assessed using measures such as grip/pinch strength, validated questionnaires, and functional outcome testing. Occlusion training can potentially serve as a specialty intervention for rehabilitation patients, reduce the cost of care, and improve the treatment options for both patients and providers.

Key facts

Study ID

NCT03056950

Run by

Brooke Army Medical Center

People needed

52

Starts

2016-03-01

Expected to finish

2019-03-01

Last updated by the study team

2017-02-20

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Status post distal radius fracture (non-operative treated with cast immobilization)
• Males and females 18-65 years of age
• Eligible to receive care at Military Treatment Facility (DEERS eligible)
• Must be able to read and write in English in order to consent

You may not qualify if…

• Contralateral upper extremity involvement resulting in less than normal range of motion, muscle strength, or daily pain greater than 1/10.
• Status post distal radius fractured treated operatively (k-wires, ORIF, etc)
• Pregnancy - per patient self-report. Due the expected small number of pregnant individuals and resulting inability to account for its effect on resulting outcomes, these patients will not be included in the study.
• Recent history of deep vein thrombosis, within the 12 months or on active treatment with anticoagulants
• History of upper quadrant lymph node dissection
• History of endothelial dysfunction
• Patient endorsement of easy bruising
• Active Infection in the injured arm
• Cancer (current diagnosis per medical record)

Where it is running

• Brooke Army Medical Center — San Antonio, Texas, United States (enrolling)

Full record on ClinicalTrials.gov

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