Comparing two rehabilitation methods after ACL surgery
Comparison of Two Different Rehabilitation Approaches Applied After Anterior Cruciate Ligament Reconstruction
This study tests two different rehab methods for athletes recovering from ACL surgery to see which one helps them recover better and avoid future injuries.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 40 (estimated) |
| Ages | 18 Years to 40 Years |
| Sex | All |
| Sponsor | Marmara University Academic / other |
| Locations | 1 site (Istanbul, Maltepe) |
| Trial ID | NCT06831279 on ClinicalTrials.gov |
What this trial studies
This study compares two different rehabilitation approaches for patients recovering from anterior cruciate ligament (ACL) reconstruction. It focuses on the importance of restoring knee function, particularly for athletes, by incorporating exercises that address both physical and cognitive tasks. Participants will engage in specific rehabilitation exercises designed to enhance their recovery and prepare them for the demands of their sport. The study aims to determine which rehabilitation method is more effective in preventing future injuries and improving overall knee stability.
Who should consider this trial
Good fit: Ideal candidates are individuals aged 18 to 40 who have undergone ACL reconstruction using a hamstring tendon autograft and are between 1 week to 1 year post-surgery.
Not a fit: Patients with cardiovascular diseases, additional lower extremity disabilities, or neurological disorders affecting balance may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved rehabilitation protocols that enhance recovery and reduce the risk of re-injury for athletes after ACL surgery.
How similar studies have performed: Other studies have shown promising results with similar rehabilitation approaches, indicating potential for success in this area.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Undergoing anterior cruciate ligament (ACL) reconstruction. Use of hamstring tendon autograft. Age between 18 and 40 years. At least 1 week but no more than 1 year post-surgery. Exclusion Criteria: * Presence of cardiovascular diseases. Any additional lower extremity disability (e.g., revision ACL reconstruction, other knee surgeries). Diagnosis of back or lumbar pain. Any neurological disorders that could affect balance (e.g., epilepsy). Presence of posterior cruciate ligament (PCL) tear in addition to ACL injury.
Where this trial is running
Istanbul, Maltepe
- Marmara University — Istanbul, Maltepe, Turkey (Türkiye) (Recruiting)
Study contacts
- Study coordinator: Gökçe Ünal, Physical Therapist
- Email: gokceharput@gmail.com
- Phone: 05319449390
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.