TASK-ORIENTED REHABILITATION AFTER ROTATOR CUFF SURGERY

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorMedipol University

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

30 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Medipol University

Lead sponsor

Fatih Sultan Mehmet Training and Research Hospital

Collaborator