MedTrace Logo

TASK-ORIENTED REHABILITATION AFTER ROTATOR CUFF SURGERY

NCT07665541 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2026-06-24

No results posted yet for this study

Summary

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.

Conditions

  • Rotator Cuff Tear Repair

Interventions

BEHAVIORAL

Task-oriented rehabilitation

In this intervention, following rotator cuff surgery, task-oriented occupational therapy sessions based on activities of daily living will be applied. These sessions will be conducted twice a week for 10 weeks and aim to achieve improvements in participants' activity performance and activity satisfaction.

BEHAVIORAL

Conventional rehabilitation group

This intervention includes exercises aimed at improving joint range of motion, enhancing muscle strength, and supporting muscle flexibility.

Sponsors & Collaborators

  • Fatih Sultan Mehmet Training and Research Hospital

    collaborator OTHER

  • Medipol University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-06-30
Primary Completion
2026-09-28
Completion
2026-10-19

Countries

  • Turkey (Türkiye)

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07665541 on ClinicalTrials.gov