Track this trial free. DataLookout checks ClinicalTrials.gov daily and emails you which fields changed on NCT07383038 (status, enrollment, completion dates, endpoints, sites) when this record is updated. Free accounts track up to 5 trials.

Track this trial

Effect of Mobilization With Movement in Patients With Rotator Cuff Lesions

StatusRecruiting
PhaseNot applicable
Started2025-08-25
View on ClinicalTrials.gov ↗
Record status
This record was last updated June 8, 2026 (before its estimated August 25, 2026 completion). Its status may not reflect the trial's current state.

Amendment history

2026-06-05
notable
Study Identification, Study Status, Study Description, Study Design, Arms and Interventions v1
Primary completion pushed: 2026-04-25 → 2026-08-25
Completion pushed: 2026-04-28 → 2026-08-28
Study description+15 characters
[...] t (MWM) group, (2) conventional physiotherapy group, or (3) controltask oriented training group. Randomization will be performed after baseline asses [...]
2026-01-28
minor
Original filing
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.
Trial Details
NCT Number NCT07383038
Lead Sponsor Kirsehir Ahi Evran Universitesi
Conditions Rotator Cuff Tears, Physical Disability
Enrollment 75 participants
Start Date 2025-08-25
Primary Completion 2026-08-25 (estimated)
Study Completion 2026-08-28 (estimated)
Updated on ClinicalTrials.gov 2026-06-08