NCT06723730 ADDITIONAL EFFECTS OF MOBILIZATION WITH MOVEMENT WITH UPPER QUADRANT CORE STRENGTHENING IN ROTATOR CUFF RELATED PAIN:A RANDOMIZED CONTROLLED TRAIL
| NCT ID | NCT06723730 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Foundation University Islamabad |
| Condition | Rotator Cuff Syndrome |
| Study Type | INTERVENTIONAL |
| Enrollment | 40 participants |
| Start Date | 2024-07-18 |
| Primary Completion | 2025-06-01 |
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 40 participants in total. It began in 2024-07-18 with a primary completion date of 2025-06-01.
⚠ 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
This study is a randomised control trial and the purpose of this study is to determine the additional effects of mobilization with movement with upper quadrant core strengthening in rotator cuff related pain .
Eligibility Criteria
Inclusion Criteria: * Age 18-65 years * Both genders * Unilateral shoulder pain of traumatic origin * Scoring should be less than 8 on numeric pain rating scale * Symptoms lasting more than 6 weeks * Pain on active shoulder movement * Pain provoked by atleast three of the following tests. A. Neer test B. Hawkins-Kennedy test C. Empty Can test D. Full Can test E. Painfull Arc test F. Resisted external rotation test * Patients reffered by a rehabilitation and orthopedic specialistwith diagnosis of rotator cuff injury, subacromial impingement syndrome, subacromial pain Exclusion Criteria: * History and Clinical presentation compatible with complete rotator cuff or bicep brachia rupture * Adhesive capsulitis * History of dislocation * Glenohumeral osteoarthritis * Cancer * Auto-immune inflammatory conditions and infection * Positive joint integrity tests ( Ant. and Post. Drawer tests) * Hill sachs lesions * Bankarts lesions * Cervical rib * Previous shoulder or neck surgery or fracture * Familiar pain provoked by neck movements * Presence of radicular sign * Diagnosis of fibromyalgia * Clinical depression * Rheumatoid arthritis * Poor bone quality ( osteoporosis) * Vertobrobasilar insufficiency test
Contact & Investigator
Frequently Asked Questions
Who can join the NCT06723730 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, up to 65 Years, studying Rotator Cuff Syndrome. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06723730 currently recruiting?
Yes, NCT06723730 is actively recruiting participants. Contact the research team at raimarana@gmail.com for enrollment information.
Where is the NCT06723730 trial being conducted?
This trial is being conducted at Rawalpindi, Pakistan.
Who is sponsoring the NCT06723730 clinical trial?
NCT06723730 is sponsored by Foundation University Islamabad. The trial plans to enroll 40 participants.