Clinical Trial

Blood Flow Restriction Exercise-induced Hypoalgesia

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Record status
This record was last updated April 11, 2025 (before its estimated August 29, 2025 completion). Its status may not reflect the trial's current state.
Summary
The goal of this crossover randomized clinical trial is to compare the acute effect on exercise-induced hypoalgesia (EIH) between isometric exercise with blood flow restriction (BFR) and isometric exercise alone in adults undergoing arthroscopic rotator cuff repair. It is presumed that the addition of BFR to isometric exercises induces a greater effect in EIH. Patients who agree to participate in this research will be randomly assigned to two intervention sequences (AB or BA), where intervention A (experimental) corresponds to isometric exercises with BFR, and intervention B (control) corresponds to isometric exercises alone. For one week, each participant attended two sessions, separated by a 72-hours wash-out period. The primary variables will be the pressure pain threshold (PPT) and conditioned pain modulation (CPM). Secondary variables will be the pain intensity and distribution, kinesiophobia, upper extremity disability, and quality of life. Results will be measured before intervention (T1, pre-intervention), immediate after intervention (T2, post-intervention 1) and 10 minutes after intervention (T3, post-intervention 2).
Trial Details
NCT Number NCT06924112
Lead Sponsor University of Valencia
Conditions Rotator Cuff Injury, Rotator Cuff Tear, Rotator Cuff Repair
Enrollment 22 participants
Start Date 2025-05-01
Primary Completion 2025-08-29 (estimated)
Study Completion 2025-09-30 (estimated)
Updated on ClinicalTrials.gov 2025-04-11