About this trial
The goal of this clinical trial is to determine the effectiveness of postoperative standard exercises with blood flow restriction therapy (BFRT) versus standard exercises alone on shoulder muscle strength and mass in participants with surgically treated rotator cuff tear. It is presumed that the addition of BFRT will significantly improve the shoulder strength and muscle mass at the end of the intervention period compared to the group receiving only standard exercises.
Patients who agree to participate in this research will be randomly assigned to a control group (standard exercises alone) or an experimental group (standard rehabilitation with BFRT). The duration of the postoperative intervention will be 12 weeks. The primary variables will be the shoulder muscle strength and muscle mass. Secondary variables will be the active shoulder mobility, pain intensity, upper limb disability, and health-related quality of life. Results will be measured at 0, 4 and 12 weeks postoperative.
Eligibility criteria
Qualifiers
Age between 40-65 years
Symptomatic degenerative rotator cuff tear diagnosed by magnetic resonance imaging
Undergoing arthroscopic rotator cuff repair
Be able to read and understand Spanish
Disqualifiers
Massive irreparable rotator cuff tear
Concomitant fracture
Labral or nerve injury
Suspicious of developing a frozen shoulder
Trial design
Treatments tested in this trial
- Standard rehabilitation
- Blood Flow Restriction Therapy