Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
ID07232511

Differences in Exercise-induced Hypoalgesia After a Session With Different Blood Flow Restriction Protocols in People With Rotator Cuff-related Shoulder Pain

Led by University of Valencia · Updated on 2026-05-04

30

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating how different blood flow restriction (BFR) exercise protocols affect pain relief and exercise tolerance in people with rotator cuff-related shoulder pain. This study compares four single exercise sessions varying in intensity (30% repetition maximum) and arterial occlusion pressure (30%, 50%, 70%, and a sham without pressure) to understand their impact on acute pain reduction. Participants will perform three specific shoulder exercises—external rotation, internal rotation, and elevation in the scapular plane—in four different sessions. Each session involves 4 sets with repetitions to fatigue at 30% repetition maximum, combined with varying blood flow restrictions or a sham cuff. Rest periods of 30 seconds between sets and 2 minutes between exercises are included. The sessions are randomized and double-blinded to compare the effects of the different BFR intensities. During the study, participants will have their pain intensity at rest and during movement measured using a visual analogue scale. Researchers will also assess pressure pain threshold, exercise tolerance, muscle activity through surface electromyography, and monitor for adverse effects immediately after and up to 24 hours post-intervention. Each participant completes all four exercise sessions, allowing detailed comparison of each protocol's effects on pain and tolerance over the study period ending in December 2026.

CONDITIONS

Brief Title

Exercise-induced Hypoalgesia Effects of Blood Flow Restriction in People With Rotator Cuff-related Shoulder Pain

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 65 years
  • Shoulder symptoms lasting at least 3 months
  • Pain in the front and side of the shoulder worsened by lifting the arm sideways
  • At least two positive results from these tests: Jobe test, resisted external rotation test, Hawkins-Kennedy test, Neer test, painful arc between 60 and 120 degrees of shoulder abduction
Not Eligible

You will not qualify if you...

  • Previous shoulder trauma or surgery
  • Pain too severe to perform the exercises
  • Unable to actively lift arm at least 90 degrees
  • Signs of a complete shoulder tear
  • Suspected frozen shoulder with significant loss of shoulder rotation
  • Primary shoulder instability or acromioclavicular joint problems
  • Shoulder pain caused mainly by neck or upper back issues
  • Corticosteroid injections within the last 6 weeks
  • Diseases like inflammatory arthritis, neurological disorders, fibromyalgia, cancer, or polymyalgia rheumatica
  • More than one risk factor for blood clots
  • Participation in upper limb exercise programs in the past month

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

screening and enrollment visit

Implementation

Duration - 1 day

Participants undergo a single session of resistance exercise with different levels of blood flow restriction applied via a cuff on the shoulder.

1 in-person session

Follow-up

Duration - 24 hours

Participants are monitored for adverse effects and exercise tolerance immediately after the session and up to 24 hours later.

Assessments immediately after, at 1 hour, 6 hours, and 24 hours post-session

Trial Site Locations

Total: 1 location

1

Faculty of Physiotherapy, University of Valencia

Valencia, Valencia, Spain, 46010

Actively Recruiting

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Research Team

A

Adrian Escriche-Escuder, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

TREATMENT

Number of Arms

4

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