TASK-ORIENTED REHABILITATION AFTER ROTATOR CUFF SURGERY

Starting soon · Not applicable

Conditions studied: Rotator Cuff Tear Repair

In brief

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.

Key facts

Study ID

NCT07665541

Run by

Medipol University

People needed

30

Starts

2026-06-30

Expected to finish

2026-10-19

Last updated by the study team

2026-06-24

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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
• Voluntary agreement to participate in the study

You may not qualify if…

• - 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
• Participation in another rehabilitation program during the study period

Where it is running

• Istanbul Medipol University — Istanbul, Istanbul, Turkey (Türkiye)

Full record on ClinicalTrials.gov

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