Blood Flow Restriction Exercise-induced Hypoalgesia

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age40-65
SponsorUniversity of Valencia

About this trial

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).

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 RC tears, concomitant fracture, labral or nerve injury.

Suspicion of developing/diagnosis a frozen shoulder.

Revision surgery after RC repair.

Previous corticosteroid injection (< 1 year).

Trial design

Treatments tested in this trial

  • Isometric exercises
  • Isometric exercises with BFR

Treatment groups

22 Participants
are divided into 2 treatment groups

Sponsors and collaborators