About this trial
Rotator cuff tears negatively affect shoulder stability, range of motion, and performance in daily activities. Postoperative rehabilitation is essential for improving functional recovery and quality of life; however, conventional approaches may not directly target meaningful activity performance.
Task-oriented occupational therapy is a client-centered approach focusing on meaningful and goal-directed activities to enhance functional independence. This randomized controlled trial aims to investigate the effect of task-oriented occupational therapy on activity participation, occupational performance, satisfaction, and functional recovery after rotator cuff surgery.
A total of 30 participants will be randomly assigned to either a task-oriented occupational therapy group or a conventional rehabilitation group. The intervention will be conducted twice weekly for 10 weeks, with 40-minute sessions based on individually prioritized activities identified using the Canadian Occupational Performance Measure. Outcomes will include occupational performance and satisfaction, goal attainment, shoulder function, quality of life, and patient satisfaction.
Eligibility criteria
Qualifiers
Individuals aged 18 years and older
Individuals who have undergone rotator cuff surgery
Medically stable and cleared for participation in a rehabilitation program
Ability to understand and follow instructions
Disqualifiers
- Presence of severe neurological disorders affecting upper extremity function
Severe cognitive impairment limiting participation
Additional musculoskeletal conditions affecting the upper extremity
Postoperative complications that may interfere with rehabilitation
Trial design
Treatments tested in this trial
- Task-oriented rehabilitation
- Conventional rehabilitation group
Treatment groups
Sponsors and collaborators
Medipol University
Lead sponsor
Fatih Sultan Mehmet Training and Research Hospital
Collaborator