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Starting soon Not applicable

Therapeutic Benefits of a Motor Imaging Protocol Following Anterior Cruciate Ligament Reconstruction Surgery

NCT07210489 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2026-10
Last updated
2026-09-21

Condition(s) studied

Anterior Cruciate Ligament Tear

Investigational drug(s) / intervention(s)

Reconstructive surgery after anterior cruciate ligament rupturesessions from a physical therapist

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

Study summary

The purpose of this study is to compare changes in lower limb symmetry during functional and strength tests, before and after the motor imagery program, in patients who received the 3-week motor imagery program starting 3 months post-surgery versus patients who did not receive the motor imagery program.

Eligibility

Sex
ALL
Min age
18 Years
Max age
45 Years
Healthy volunteers
No
Inclusion Criteria: * Patients aged 18 to 45; * Individuals who have undergone anterior cruciate ligament reconstruction for the first time on the operated leg; * Patients able to understand and read French; * Affiliation with a social insurance plan; * Signed informed consent. Exclusion Criteria: * Recurrence or rupture of the contralateral anterior cruciate ligament; * History of another orthopedic surgery on the ipsilateral and/or contralateral lower limb; * History of an injury to the ipsilateral and/or contralateral lower limb within the last 3 months; * Osteotomy; * Cognitive disorders observed by the investigator for inclusion ; * Vestibular disorders known to the patient or observed by the investigator for inclusion; * 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.

Primary outcome measure(s)

  • Evolution of limb symmetry — between 3 and 4.5 months
    Evolution of limb symmetry assessed by the Limb Symmetry Index in %
  • Isometric quadriceps strength — between 3 and 4.5 months
    Isometric quadriceps strength using a Micro Fet handheld dynamometer (in Newtons)
  • Isometric hamstring strength — between 3 and 4.5 months
    Isometric hamstring strength measured using a Micro Fet handheld dynamometer (in Newtons)
  • Average concentric strength — between 3 and 4.5 months
    Average concentric strength during a counter-movement jump measured using a force platform (in Newtons)
  • Average strength — between 3 and 4.5 months
    Average strength during a squat measured using a force platform (in Newtons)
  • Quadriceps activation measured — between 3 and 4.5 months
    Quadriceps activation measured using electromyography

Trial sites (1)

FacilityCityRegionStatus
Clinique de la Sauvegarde Lyon France
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07210489 on ClinicalTrials.gov ↗ ← All trials in France