Evaluating a scale for assessing landing quality after ACL reconstruction
Validity of the SHD-LESS Scale in Detecting Landing Asymmetry and Its Association With Functional Status After ACL Reconstruction.
University Hospital, Caen · NCT06829849
This study is testing a new scale to see how well it can measure landing quality in young adults who have had ACL surgery, to help understand their recovery and performance.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 55 (estimated) |
| Ages | 18 Years to 40 Years |
| Sex | All |
| Sponsor | University Hospital, Caen (other) |
| Locations | 1 site (Caen) |
| Trial ID | NCT06829849 on ClinicalTrials.gov |
What this trial studies
This observational study aims to validate the SHD-LESS scale, which assesses landing quality during a Single Hop for Distance (SHD) task in patients who have undergone anterior cruciate ligament reconstruction (ACL-R). The study will evaluate the scale's effectiveness in identifying asymmetrical landing patterns and differences between the operated and uninjured limbs. Additionally, it will explore the association of landing quality with knee muscle strength, functional status, and psychological readiness. Participants will be patients aged 18-40 who are at least six months post-ACL-R and are part of a sports medicine care pathway.
Who should consider this trial
Good fit: Ideal candidates are individuals aged 18-40 who have had a first ACL reconstruction more than six months ago and are being monitored in a sports medicine program.
Not a fit: Patients with previous lower limb ligament surgeries, complex ligament injuries, or recent muscle injuries may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance return-to-sport assessments and reduce the risk of re-injury in athletes recovering from ACL reconstruction.
How similar studies have performed: While the SHD-LESS scale has shown reliability in healthy individuals, this study is novel in its application to post-ACL reconstruction patients.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients aged 18-40, who have undergone a first ACL reconstruction more than 6 months ago and are being followed in a sports medicine care pathway * Affiliated with a health insurance plan * Information form: Non-objection to the use of data for research purposes Exclusion Criteria: * Previous ligament surgery of the lower limbs prior to ACL reconstruction * Complex ligament injury (lateral ligaments, posterior cruciate ligament) * Recent muscle injuries * History of injury to the uninjured knee * Pregnant woman * Inability to perform a muscular assessment * Postoperative complications (deep vein thrombosis, sepsis, stiffness/arthrofibrosis) * Neurological history with residual effects or taking medication that affects balance/coordination
Where this trial is running
Caen
- Service de Médecine du sport, CHU Caen — Caen, France (RECRUITING)
Study contacts
- Study coordinator: Joffrey DRIGNY, Associate Prof, MD PhD
- Email: drigny-j@chu-caen.fr
- Phone: +33 02 31 06 45 33
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.
Conditions: ACL Reconstruction, ACL Injury