Trials / Recruiting
RecruitingNCT07135375
Postoperative Rotator Cuff Rehabilitation: Functional, Pain and Sleep Quality
Postoperative Rotator Cuff: Functional, Pain and Sleep Quality
- Status
- Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 50 (estimated)
- Sponsor
- LAURA CASTILLO VEJAR · Academic / Other
- Sex
- All
- Age
- 50 Years
- Healthy volunteers
- Not accepted
Summary
Rotator cuff injuries are the third leasing cause of pain and disability, accounting for 16% of all musculoskeletal injuries. Following surgical intervention, patients typically undergo a 4 to 6 week immobilization period before starting physical therapy. This rehabilitation phase can last between 4 to 6 months. Despite this, there is currently a lack of clear guidelines regarding specific physical therapy protocols or the expected post surgical recovery for patients who have undergone rotator cuff repair.
Detailed description
Objective: To compare the effectiveness of a differentiated rehabilitation protocol based on the number of tendons repaired versus a standard rehabilitation protocol, regarding functionality, pain, subjective perception of sleep quality, and mobility, in patients who have undergone surgical rotator cuff repair.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Rehabilitation protocol | The modified protocol will be implementen based on available scientific evidence and guided by the consensus remaches with the traumatologist at the physiotherapy center |
Timeline
- Start date
- 2025-08-26
- Primary completion
- 2025-11-30
- Completion
- 2026-03-30
- First posted
- 2025-08-22
- Last updated
- 2025-09-10
Locations
2 sites across 1 country: Chile
Source: ClinicalTrials.gov record NCT07135375. Inclusion in this directory is not an endorsement.