Effect of Scapular Stabilization Exercises on Pain and Functional Outcomes in Subacromial Impinge… (NCT07277868) | Clinical Trial Compass
CompletedNot Applicable
Effect of Scapular Stabilization Exercises on Pain and Functional Outcomes in Subacromial Impingement Syndrome: A Randomized Controlled Trial
Turkey (Türkiye)60 participantsStarted 2025-08-30
Plain-language summary
This randomized controlled study aims to evaluate the effects of scapular stabilization exercises on pain, shoulder function, and quality of life in patients with subacromial impingement syndrome. Participants will be randomly assigned to either a scapular stabilization exercise program or a conventional shoulder rehabilitation program. Pain, functional outcome measures, and patient-reported quality of life will be assessed at baseline, 4 weeks, and 12 weeks. The study seeks to determine whether adding scapular stabilization exercises provides superior clinical benefit.
Who can participate
Age range
18 Years – 65 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Adults aged 18 to 65 years.
* Clinically diagnosed subacromial impingement syndrome (SIS) based on:positive Neer test ,positive Hawkins-Kennedy test ,painful arc between 60°-120°,pain during resisted shoulder tests
* Symptoms present for at least 4 weeks.
* Ability to comply with a 12-week supervised rehabilitation program.
* Ability to provide written informed consent.
Exclusion Criteria:
* Previous shoulder surgery on the affected side.
* Presence of full-thickness rotator cuff tear confirmed by ultrasound imaging.
* Evidence of cervical radiculopathy or significant cervical spine pathology.
* Advanced glenohumeral or acromioclavicular osteoarthritis.
* History of inflammatory rheumatic diseases (e.g., rheumatoid arthritis, ankylosing spondylitis).
* Severe cardiopulmonary, neurological, or systemic conditions limiting physical activity.
* Recent shoulder fracture or dislocation (\< 6 months).
* Participation in another structured shoulder rehabilitation program within the last 3 months.
* Pregnancy.
* Inability to understand or follow instructions required for the intervention or assessments.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
1. Quick Disabilities of the Arm, Shoulder and Hand (QuickDASH) Score
Timeframe: Baseline, Week 6, Week 12
Trial details
NCT IDNCT07277868
SponsorKanuni Sultan Suleyman Training and Research Hospital