Clinical Trials Directory

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

TypeNameDescription
OTHERRehabilitation protocolThe 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.