Optimized Rehabilitation After Anterior Cruciate Ligament Before Returning to Sport
NCT ID: NCT05323474
Last Updated: 2025-05-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
NA
432 participants
INTERVENTIONAL
2022-11-14
2027-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
This multicentre randomized control trial aims to evaluate the effectiveness of an individualized and optimized rehabilitation program guided by monthly assessments carried out by physiotherapists from the 3rd to the 6th month postoperatively to reduce the risk of new ACL injuries (operated or healthy knee), compared to standard management.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Prolonged Preoperative Rehabilitation in ACL Rupture.
NCT04888052
Safe Return to Play After ACL Reconstruction
NCT04827264
Immediate Versus Optional Delayed Surgical Repair for Treatment of Acute ACL Injuries
NCT05747079
Predictive Factors for a Successful Return to Run After ACL-R
NCT04130308
Description of Return to Sport in Amateur Athletes Who Underwent Several Functional Tests (K-STARTS, Vertical Jumps and Soleus Muscle Strength) After Initial ACL Reconstruction
NCT07249645
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Standard rehabilitation
Classical rehabilitation carried out by a physiotherapist with an evaluation at 6 months post-surgery to authorize the return to sport.
Usual rehabilitation
Usual rehabilitation according to the practice of the "Haute Autorité de Santé" (HAS)
Optimized rehabilitation
Classical rehabilitation carried out by a physiotherapist + expert physiotherapist performing monthly clinical and functional assessments with recommendations for exercises and running program sent to the physiotherapist.
Rehabilitation optimized
Rehabilitation optimized according to the study protocol
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Usual rehabilitation
Usual rehabilitation according to the practice of the "Haute Autorité de Santé" (HAS)
Rehabilitation optimized
Rehabilitation optimized according to the study protocol
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Patient who has had an ACL reconstruction regardless of the standard surgical technique used
* Patient with a sports activity, pivot and/or contact (e.g. soccer, basketball, handball, rugby, judo...) and practiced in competition (Tegner sports activity scores \>7 and Marx scores \>11 before the accident.
* Patient wishing to return to competitive sport
* Consent signed by the patient
Exclusion Criteria
* Patients with a medical contraindication to the performance of one of the tests
* Patients suffering from a neurological (motor and/or sensitive), vestibular or rheumatic pathology
* Patient performing rehabilitation with a physiotherapist who does not wish to participate in the study.
* Pregnant or breastfeeding woman
* Patient under guardianship or curators
18 Years
25 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Ministry of Health, France
OTHER_GOV
Centre Hospitalier Universitaire de Saint Etienne
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Thomas NERI, MD
Role: STUDY_CHAIR
CHU DE SAINT-ETIENNE
Grégory MOREL, Physio
Role: PRINCIPAL_INVESTIGATOR
CHU DE SAINT-ETIENNE
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Medipole de Savoie
Challes-les-Eaux, , France
Clinique de Domont Ortholab
Domont, , France
Centre Hospitalier de Firminy
Firminy, , France
Clinique de La Sauvegarde
Lyon, , France
Hopital de La Croix Rousse
Lyon, , France
CHU de Saint-Etienne
Saint-Etienne, , France
Hôpital de la Tour
Geneva, , Switzerland
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2022-A00287-36
Identifier Type: OTHER
Identifier Source: secondary_id
20PH282
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.