Improving recovery after PRP injections for rotator cuff tears
Effect of the Muscle Strength and Range of Motion Training for Post-platelet Rich Plasma Injection in People With Rotator Cuff Partial Tear: a Randomized, Cross-over Trial
This study is testing a new rehabilitation program for people with partial rotator cuff tears who have had PRP injections to see if it helps them recover better.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 30 (estimated) |
| Sex | All |
| Sponsor | Taipei Hospital, Ministry of Health and Welfare Academic / other |
| Locations | 1 site (New Taipei City, ROC) |
| Trial ID | NCT06192459 on ClinicalTrials.gov |
What this trial studies
This study aims to develop and evaluate a standardized rehabilitation plan for patients with partial rotator cuff tears who have received Platelet-Rich Plasma (PRP) injections. The focus is on enhancing muscle strength and joint mobility through a structured post-injection rehabilitation program. Participants will engage in modality physical therapy and combined therapy to assess the effectiveness of this approach. The study seeks to address the inconsistencies in rehabilitation practices following PRP treatment and improve overall patient outcomes.
Who should consider this trial
Good fit: Ideal candidates are individuals with partial rotator cuff tears who have undergone PRP treatment and are willing to participate in the rehabilitation program.
Not a fit: Patients with severe shoulder joint immobility or those with other significant skeletal joint issues may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved recovery and quality of life for patients with rotator cuff injuries.
How similar studies have performed: While there is limited literature on standardized rehabilitation post-PRP injection, similar approaches in other contexts have shown promise, indicating potential for success.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Patients with rotator cuff tears who have undergone PRP (Platelet-Rich Plasma) treatment. All participants must sign an informed consent form. 2. Patients must fully participate in the rehabilitation treatment throughout the study. Exclusion Criteria: 1. Patients with concomitant other skeletal joint issues, such as multiple joint arthritis, humeral or acromioclavicular joint fractures, or those who have undergone previous shoulder joint surgeries. 2. Patients with severe shoulder joint immobility or contracture preventing any joint movement, but mild to moderate joint mobility restrictions are not considered exclusion criteria. 3. Inability to comply with the two-month research project.
Where this trial is running
New Taipei City, ROC
- Taipei Hospital, Ministry of Health and Welfare — New Taipei City, Roc, Taiwan (Recruiting)
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.