- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07602478
Eccentric Contraction Exercise For Shoulder Pain Syndrome
May 16, 2026 updated by: Rafeef Hassan Asiri
Short-term Effect of Eccentric Contraction Exercises in the Treatment of Patients With Shoulder Pain Syndrome: A Randomized Controlled Trial
The current study will help to determine the efficacy of a rehabilitation protocol that involves the use of eccentric contraction for patients with shoulder pain syndrome.
This approach aims to improve recovery in terms of pain and function based on scientific evidence.
Study Overview
Status
Active, not recruiting
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
60
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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'Asir Region
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Khamis Mushait, 'Asir Region, Saudi Arabia, 62413
- Armed Forces Hospital Southern Region
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- 18-70 years old patient, female and male diagnosed with Shoulder pain syndrome and reliable patients who can follow orders.
- Patient diagnosed by rotator cuff tendinitis
Exclusion Criteria:
- Patient with VAS more than 8/10
- History of shoulder, cervical, or thoracic surgery, shoulder dislocation, fracture, and labral tear, full thickness rotator cuff tear and adhesive capsulitis, rheumatic disease and / or any medical condition that prevents patient to perform resisted exercises
- Neoplastic disease, and systemic inflammatory disease
- Participants with three positive rotator cuff tear tests were likely to have a full-thickness rotator cuff tear and were excluded from the study.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Eccentric Exercise Group
Patients in this group will receive a supervised rehabilitation protocol focusing on eccentric contractions of the shoulder muscles.
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A 6-week rehabilitation program, conducted for two sessions per week.
Patients will receive specialized eccentric contraction exercises for the shoulder muscles, administered in addition to a standard physical therapy protocol.
A 6-week standard rehabilitation program, conducted for two sessions per week.
Patients will receive Traditional physical therapy interventions only, which include ultrasound, range of motion (ROM) exercises, postural training and general strengthening routinely prescribed."
|
|
Active Comparator: Traditional Physical Therapy Group
Patients in this group will receive traditional physical therapy interventions commonly used for shoulder pain syndrome
|
A 6-week standard rehabilitation program, conducted for two sessions per week.
Patients will receive Traditional physical therapy interventions only, which include ultrasound, range of motion (ROM) exercises, postural training and general strengthening routinely prescribed."
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Change from Baseline in Pain Intensity using the Visual Analog Scale (VAS)
Time Frame: Baseline and at the end of the 6-week intervention period.
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Baseline and at the end of the 6-week intervention period.
|
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Change from Baseline in Shoulder Pain and Disability using the Shoulder Pain and Disability Index (SPADI)
Time Frame: Baseline and at the end of the 6-week intervention period.
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Baseline and at the end of the 6-week intervention period.
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Change from Baseline in Functional Independence using the Functional Independence Measure (FIM)
Time Frame: Baseline and at the end of the 6-week intervention period.
|
Baseline and at the end of the 6-week intervention period.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Camargo PR, Avila MA, Alburquerque-Sendin F, Asso NA, Hashimoto LH, Salvini TF. Eccentric training for shoulder abductors improves pain, function and isokinetic performance in subjects with shoulder impingement syndrome: a case series. Rev Bras Fisioter. 2012 Jan-Feb;16(1):74-83. doi: 10.1590/s1413-35552012000100013.
- Alizadehkhaiyat O, Roebuck MM, Makki AT, Frostick SP. POSTURAL ALTERATIONS IN PATIENTS WITH SUBACROMIAL IMPINGEMENT SYNDROME. Int J Sports Phys Ther. 2017 Dec;12(7):1111-1120. doi: 10.26603/ijspt20171111.
- Gordon F. 'Robert Schumann's mental illnesses. (Genius and madness)', by Mlle Dr Pascal (1908a): Introduction and translation by Felicia Gordon. Hist Psychiatry. 2015 Sep;26(3):359-71. doi: 10.1177/0957154X15589457.
- Kang J, Zhang Z, Wang J, Wang G, Yan Y, Qian H, Zhang X, Xu W, Mao F. hucMSCs Attenuate IBD through Releasing miR148b-5p to Inhibit the Expression of 15-lox-1 in Macrophages. Mediators Inflamm. 2019 May 28;2019:6953963. doi: 10.1155/2019/6953963. eCollection 2019.
- Shlipak M. Diabetic nephropathy: preventing progression. BMJ Clin Evid. 2010 Jul 8;2010:0606.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
October 29, 2025
Primary Completion (Actual)
January 29, 2026
Study Completion (Estimated)
December 31, 2026
Study Registration Dates
First Submitted
May 16, 2026
First Submitted That Met QC Criteria
May 16, 2026
First Posted (Actual)
May 22, 2026
Study Record Updates
Last Update Posted (Actual)
May 22, 2026
Last Update Submitted That Met QC Criteria
May 16, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- H-01-R-096
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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