About this trial
This randomized controlled trial aims to investigate the effects of Mobilization with Movement (MWM) on pain and functional status in individuals with rotator cuff lesions. Rotator cuff pathology is a common cause of shoulder pain and functional limitation, and impairments in proprioception may further compromise shoulder motor control and recovery.
Eligible participants with rotator cuff lesions will be randomly allocated into three groups: (1) Mobilization with Movement (MWM), (2) conventional physiotherapy, and (3) control group. All participants will be evaluated before and after the intervention period. Outcome measures will include shoulder-related functional disability assessed by the QuickDASH questionnaire, pain intensity, and shoulder joint position sense evaluated using an active repositioning test with a laser pointer during shoulder flexion.
The study is designed to determine whether MWM provides additional benefits over conventional treatment or task oriented training intervention in improving pain, function, and proprioceptive accuracy. The findings are expected to contribute to evidence-based conservative rehabilitation strategies for patients with rotator cuff lesions.
Eligibility criteria
Qualifiers
Age between 18 and 65 years
Clinical and/or imaging-confirmed diagnosis of rotator cuff lesion (e.g., tendinopathy or partial tear)
Presence of shoulder pain for at least 3 months
Pain and functional limitation during shoulder movements
Disqualifiers
History of shoulder surgery on the affected side
Full-thickness rotator cuff tear or shoulder instability
Shoulder fracture, dislocation, or acute trauma within the past 6 months
Neurological disorders affecting the upper extremity (e.g., cervical radiculopathy, peripheral neuropathy)
Trial design
Treatments tested in this trial
- Mulligan mobilization
- Conventional Physiotherapy