Effects of movement mobilization and core strengthening on shoulder pain
Official title: ADDITIONAL EFFECTS OF MOBILIZATION WITH MOVEMENT WITH UPPER QUADRANT CORE STRENGTHENING IN ROTATOR CUFF RELATED PAIN:A RANDOMIZED CONTROLLED TRAIL
Run by Foundation University Islamabad · NCT06723730 · Data updated 2026-11-12
This study is testing if a combination of movement therapy and core strengthening exercises can help people with rotator cuff-related shoulder pain feel better.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 65 Years |
| Sex | All |
| Enrollment | 40 (estimated) |
| Sponsor | Foundation University Islamabad Academic / other |
| Locations | 1 site (Rawalpindi, Punjab Province) |
| Status | Recruiting |
| Started | July 18, 2024 |
| Main results expected | June 1, 2025 |
| Study ends | June 20, 2025 |
| Registry record updated | December 9, 2024 |
| Trial ID | NCT06723730 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are individuals aged 18-65 with unilateral shoulder pain of traumatic origin lasting more than six weeks.
✕Probably not a fit
Patients with complete rotator cuff tears, adhesive capsulitis, or significant joint integrity issues may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This clinical trial aims to evaluate the additional effects of mobilization with movement combined with upper quadrant core strengthening on patients suffering from rotator cuff-related shoulder pain. Participants will be randomly assigned to treatment groups, and their pain levels, range of motion, proprioception, and kinesiophobia will be assessed. The study will involve a structured intervention protocol and will collect data through various pain assessment tests. Informed consent will be obtained from all participants prior to enrollment.
Why it matters
Potential benefit: If successful, this approach could significantly improve pain management and functional outcomes for patients with rotator cuff-related pain.
How similar studies have gone: While similar approaches have been explored, this specific combination of interventions is relatively novel and has not been extensively tested.
Who can join: the full rules
Show full inclusion / exclusion 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
Where it's running
-
Foundation University College of Physical Therapy
Rawalpindi, Punjab Province, Pakistan Recruiting
Study contacts
- Study coordinator: Raima Liaqat, MS-MSKPT*
- Email: raimarana@gmail.com
- Phone: 0302-9670275
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Does age-related muscle loss change rotator cuff tear patterns?
We will see if age-related muscle loss (sarcopenia) is linked to the location and type of rotator cuff tears in adults aged 40–75 with rotator cuff syndrome.
-
Local versus general plus local anesthesia for arthroscopic rotator cuff repair
This trial tests whether local/regional anesthesia alone or general anesthesia plus local/regional anesthesia helps adults recover consciousness and stable breathing/heart function faster after arthroscopic rotator cuff repair.
-
Registry to evaluate outcomes of FX Shoulder replacement devices
This study is setting up a registry to see how well FX Shoulder replacement devices work for patients after their surgeries over the next few years.
-
Evaluating outcomes of FX Shoulder Solutions implants for shoulder conditions
This study is testing how well FX Shoulder Solutions implants work for people who have had shoulder replacement surgeries to see if they help patients recover safely and effectively.
-
Regeneten implant to help rotator cuff repair
Aims to see if adding Regeneten bioinductive membrane during rotator cuff repair helps the tendon heal better in adults with distal lesions.
-
Rotator cuff repair with biceps rerouting and dermal graft augmentation for large, difficult tears
This study tests a combined surgical approach to see if it helps tendon retear rates in adults with large rotator cuff tears that are hard to repair.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.