Evaluating psychological factors affecting recovery after ACL reconstruction
Psychological Factors Influencing the Patient-reported and Functional Outcome of ACL Reconstruction and Their Sex-specific Differences
This study is trying to see how mental factors affect recovery for people who have had ACL surgery, and whether these effects are different for men and women.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 100 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Medical University of Vienna Academic / other |
| Locations | 1 site (Vienna) |
| Trial ID | NCT06156501 on ClinicalTrials.gov |
What this trial studies
This study investigates how psychological factors influence the recovery outcomes reported by patients who have undergone ACL reconstruction. It aims to assess both patient-reported outcomes and functional results, with a focus on identifying any differences based on sex. By prospectively evaluating these psychological parameters, the study seeks to enhance understanding of their role in recovery and rehabilitation processes following ACL injuries.
Who should consider this trial
Good fit: Ideal candidates for this study are adults over 18 years old who have suffered an ACL tear and have no preexisting knee conditions.
Not a fit: Patients under 18 years old or those with preexisting knee conditions or additional knee injuries may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved recovery strategies tailored to individual psychological profiles, enhancing patient outcomes after ACL reconstruction.
How similar studies have performed: While the specific focus on psychological factors in ACL reconstruction is less common, similar studies have shown that psychological well-being can significantly impact recovery outcomes in various orthopedic conditions.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * ACL tear * Over 18 years * Patient information and consent * No preexisting knee conditions prior ACL tear; Exclusion Criteria: * Under 18 years * Preexisting knee conditions * Accompanying knee injuries apart from ACL tear
Where this trial is running
Vienna
- Medical University of Vienna — Vienna, Austria (Recruiting)
Study contacts
- Study coordinator: Lorenz Pichler, MD
- Email: lorenz.pichler@meduniwien.ac.at
- Phone: +43 1 40400-56190
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.