A Randomized Controlled Trial on the Effectiveness of Early Versus Conservative Rehabilitation Following Rotator Cuff Repair
Starting soon · Not applicable
Conditions studied: Rotator Cuff Tear
In brief
Background Rotator cuff tears (RCTs) are a common, costly, and often persistent musculoskeletal complaint, with an increasing number of shoulder pain patients undergoing surgical repair each year. Whereas many asymptomatic RCTs can be successfully managed non-surgically, when conservative treatment fails, surgery is recommended. However, there is a lack of consensus on the best approach to postoperative rehabilitation, an important factor in the recovery process of rotator cuff repairs. This study aims to investigate the effectiveness of early versus delayed rehabilitation following rotator cuff repairs. Objective This study aims to determine the effectiveness of early versus delayed rehabilitation following rotator cuff repairs. Method A two-armed, randomized controlled trial will be conducted in an outpatient physical rehabilitation department at a tertiary hospital. The sample will include 88 adults aged 18 years or older with RCTs. From the day after surgery, the intervention will engage in supervised passive range of motion (ROM) exercises, focusing on forward flexion and external rotation. They will receive daily exercise instructions, including table slides and active movements for the elbow, wrist, and hand, while also practicing passive shoulder flexion and abduction based on their pain limits. Participants are encouraged to do gentle pendulum exercises and passive movements three times daily to improve shoulder mobility. Active shoulder exercises will be restricted until six weeks post-surgery to ensure healing. Sling use will decrease by the sixth week, allowing for active ROM exercises to start. Participants in the control group will follow a delayed rehabilitation protocol, learning strict sling immobilization techniques for the first six weeks postoperatively. During this period, sling removal will be allowed only for basic exercises and daily activities, with no other shoulder movements encouraged initially. Sling use will end by the sixth week, followed by the start of active ROM exercises. Outcome measures will include shoulder ROM, muscle power, a numeric pain scale (NPS), shoulder pain disability index (SPADI), and EQ-5D-5L questionnaires assessed at 3, 6, and 12 months follow-up between the two groups. Rotator cuff integrity will be evaluated using MRI at baseline and at 12 months post-surgery. Conclusion We anticipate that this study will add to the body of knowledge required to make effective treatment choices on the management of patients following rotator cuff repairs. Ultimately, this trial aims not only to influence national rehabilitation guidelines but also to enrich the global evidence base concerning optimal rehabilitation strategies following rotator cuff repair, especially for populations in the Middle East and Gulf regions.
Key facts
- Study ID
- NCT07324174
- Run by
- King Faisal Specialist Hospital & Research Center
- People needed
- 86
- Starts
- 2026-01-01
- Expected to finish
- 2029-12-30
- Last updated by the study team
- 2026-01-09
Who can join
Age: 17 and older, up to 100. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adults aged 18 years and older
- Patients diagnosed with a symptomatic tear of the rotator cuff and listed for surgical repair
- Rotator cuff tear confirmed by MRI
- Patients screened by the surgeon as suitable to participate
- Able to attend out-patient follow-up physiotherapy appointment
- Demonstrate the ability and willingness to consent and continue participation in the study
- Able to understand Arabic or English Language
You may not qualify if…
- A patient will not be eligible for participation in the study if any of the following criteria apply:
- Individuals younger than 18 years
- Those unable or unwilling to consent or continue with the study.
- Moderate to severe arthritis seen on x rays or MRI
- Fatty infiltration grade >= 3
Where it is running
- King Faisal Specialist Hospital and Research Centre — Riyadh, Saudi Arabia
Full record on ClinicalTrials.gov
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