Therapeutic Benefits of a Motor Imaging Protocol Following Anterior Cruciate Ligament Reconstruction Surgery
NCT ID: NCT07210489
Last Updated: 2026-01-15
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
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NOT_YET_RECRUITING
NA
70 participants
INTERVENTIONAL
2026-01-31
2027-03-31
Brief Summary
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Detailed Description
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The study population is composed of adult patients who underwent reconstructive surgery after anterior cruciate ligament rupture, followed up at the Clinique de la Sauvegarde in Lyon for post-operative functional and strength testing of the anterior cruciate ligament.
Patients included in the study will be randomized into two study arms (experimental arm and control arm).
Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
SINGLE
Study Groups
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Motor imagery program
Patients will receive rehabilitation sessions from a physical therapist in accordance with standard practice and will be asked to complete a 3-week motor imagery program starting 3 months after anterior cruciate ligament surgery.
Reconstructive surgery after anterior cruciate ligament rupture
surgical technique for repairing the cruciate ligament
sessions from a physical therapist
sessions from a physical therapist in accordance with standard practice
Cognitive (non-motor) task program
Patients will receive rehabilitation sessions from a physical therapist in accordance with standard practice and will be asked to complete a 3-week cognitive (non-motor) task program starting 3 months after anterior cruciate ligament surgery.
Reconstructive surgery after anterior cruciate ligament rupture
surgical technique for repairing the cruciate ligament
sessions from a physical therapist
sessions from a physical therapist in accordance with standard practice
Interventions
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Reconstructive surgery after anterior cruciate ligament rupture
surgical technique for repairing the cruciate ligament
sessions from a physical therapist
sessions from a physical therapist in accordance with standard practice
Eligibility Criteria
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Inclusion Criteria
* Individuals who have undergone anterior cruciate ligament reconstruction for the first time on the operated leg;
* All types of surgery (harvesting of the new gracilis or patellar tendon) within 3 months prior to inclusion;
* Patients able to understand and read French;
* Affiliation with a social insurance plan;
* Signed informed consent.
Exclusion Criteria
* Osteotomy;
* Cognitive disorders observed by the investigator;
* Vestibular disorders known to the patient or observed by the investigator;
* Post-surgical complications (infection, early graft rupture);
* Patient participating in another interventional clinical trial, or in a period of exclusion from another interventional study;
* Patient under guardianship or conservatorship;
* Pregnant or breastfeeding women.
18 Years
45 Years
ALL
No
Sponsors
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Euraxi Pharma
INDUSTRY
GCS Ramsay Santé pour l'Enseignement et la Recherche
OTHER
Responsible Party
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Locations
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Clinique de la Sauvegarde
Lyon, , France
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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2025-A01415-44
Identifier Type: -
Identifier Source: org_study_id
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