NCT07675655 Mulligan Mobilization Versus PNF Technique in SIS
| NCT ID | NCT07675655 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Cairo University |
| Condition | Subacromial Impingement Syndrome |
| Study Type | INTERVENTIONAL |
| Enrollment | 69 participants |
| Start Date | 2025-09-02 |
| Primary Completion | 2026-08-01 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 69 participants in total. It began in 2025-09-02 with a primary completion date of 2026-08-01.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
To investigate the differences between adding Mulligan mobilization and PNF to the conventional physical therapy program on shoulder pain, function, shoulder muscles strength, glenohumeral flexion, abduction, external rotation, and internal rotation ROM, scapular symmetry, and pectoralis minor length in patients with SIS.
Eligibility Criteria
Inclusion Criteria: 1. Sixty nine Males and females subjects with SIS, age between 20-40 years old and body mass index (BMI) 18-27.9 kg/m2 2. The SIS group will be limited to patients who had history of shoulder pain of \>1-week duration. 3. Pain localized at the proximal anterolateral shoulder region. 4. Patients with subacromial pain syndrome with positive results of 3 of 5 tests: painful arc, pain or weakness with resisted external rotation, Neer test, Hawkins Kennedy test, and Jobe/empty can test. Exclusion Criteria: * Patients will be excluded if they had any of the following conditions: 1. Open wounds, infection, acute injuries, swelling, rheumatoid arthritis, reflex sympathetic syndrome, or adhesive capsulitis. 2. BMI greater than 28 kg/m². 3. History of shoulder girdle fractures and dislocation, shoulder surgery in the last 12 months or full thickness rotator cuff tear. 4. History of systemic or neurological disorder, cervical radiculopathy and subjects who had received physical therapy treatment for their shoulder within the past three months. 5. History of corticosteroid injection in the shoulder region less than 12 weeks previously.
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07675655 clinical trial?
This trial is open to participants of all sexes, aged 20 Years or older, up to 40 Years, studying Subacromial Impingement Syndrome. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07675655 currently recruiting?
Yes, NCT07675655 is actively recruiting participants. Contact the research team at mina.magdy.9595@gmail.com for enrollment information.
Where is the NCT07675655 trial being conducted?
This trial is being conducted at Sohag, Egypt.
Who is sponsoring the NCT07675655 clinical trial?
NCT07675655 is sponsored by Cairo University. The trial plans to enroll 69 participants.