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NCT Number: NCT05323474

Optimized Rehabilitation After Anterior Cruciate Ligament Before Returning to Sport

Following reconstruction of the anterior cruciate ligament (ACL), a standardized rehabilitation protocol is carried out by a physiotherapist. In France, a well-established rehabilitation consensus guides the first phase of 3 months postoperatively and patient compliance is generally excellent. The next phase should allow a return to sport (RTS) following a continuum depending on the objectives of the sport's patient, starting with a return to running activities (RTR) and a preparatory phase for a RTS which may be authorized at 6 months post-op.

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.

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Key information

Age range

18 year–25 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Medipole de Savoie, Challes-les-Eaux, France

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About this study

Each year more than 40,000 surgical reconstructions of the anterior cruciate ligament (ACL) by ligamentoplasty are performed in France; the rupture being most often the result of sports practice. Following this surgical reconstruction of the ACL, a standardized rehabilitation protocol is carried out by a masseur-physiotherapist. A well-established rehabilitative consensus guides the first phase of the 3 months post-operative and patient compliance is generally excellent. The next phase should allow the return to sport (RTS) by following a continuum according to the objectives of the athlete patient. In this continuum, authors distinguish the return to sports activities in the axis, such as running (RTS1), preparing the return to training (RTS2), and much later will be done by the return to competition (RTS3).RTS2, which is probably the most delicate stage due to the highly variable progression from one patient to another, is generally allowed from the 6th month post-operative, after the realization and validation of a battery of tests assessing the athlete's ability to resume training.Despite this precaution, there is a major risk of new injury (20%), especially in the contralateral knee (12%) requiring new, longer, more restrictive rehabilitation care with an additional 3 to 12 months' incapacity for work or sport.. As the risk of "re-injury" of the knee seems independent of the surgical technique used and the first 3 months of rehabilitation, the rehabilitative management of this phase of 3 to 6 months post-operative appears decisive in the prevention of a new injury. The return to running (in the RTS1) therefore seems a major objective for rehabilitation and will build the necessary foundation for the resumption of the patient's favorite sport, RTS2. However, to allow the return to running, no objective criteria have been validated to date and no consensus is identifiable in the scientific literature. It is the same for his preparation and the gradual resumption of running. Thus, an optimized rehabilitation between the 3rd and 6th month, based on objective evaluations of the patient's functional abilities allowing personalized rehabilitation, including guided and individualized running training, could reduce the risk of new ACL injuries (operated or healthy knee) by better preparing the patient for RTS2: the return to his favorite sport

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Affiliation to the French Social Security system
  • 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

  • Contralateral or bilateral involvement or operated on for a re-injury of the ACL
  • 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

Treatment and study plan

Usual rehabilitation

Other

Usual rehabilitation according to the practice of the "Haute Autorité de Santé" (HAS)

Rehabilitation optimized

Other

Rehabilitation optimized according to the study protocol

Primary outcomes

  1. Number of patients with at least one new ACL injury

    Time frame: At 24 months post surgery

    A re-rupture of the operated ACL or a rupture on the contralateral side, objectified by a Lachman test performed with the absence of a "firm" stop, and a difference in laxity measured with an arthrometer ( >3 mm for the KT-1000 ™ or >3 mm for the GNRB® or >5 mm for the Telos™ ) and by an MRI diagnosing an ACL rupture.

Secondary outcomes

  1. Number of patients meeting all the criteria necessary for authorization to return to their usual sports activities

    Time frame: At 6 months post surgery

    The criteria are :

    • Recovery of symmetry of muscle strength of the Quadriceps with a Limb Symmetry Index (LSI) > 90%
    • International Knee Documentation Committee (IKDC) score > the 15th percentile of subjects of the same age
    • Anterior Cruciate Ligament-Return to Sport after Injury (ACL-RSI) score >56
  2. Number of patients with at least one post-surgical complication

    Time frame: At 24 months post surgery

    Post-surgical complications are :

    • residual flexion (>5°) measured by goniometric joint assessment,
    • knee flexion deficit (>10°) measured by goniometric joint assessment,
    • Cyclops syndrome as measured by Magnetic resonance imaging (MRI),
    • secondary symptomatic meniscal lesions objectified by a clinical examination performed by a physician and an MRI,
    • Myo-aponeurotic lesions objectified by a clinical examination performed by a physician and medical imaging (MRI or ultrasound).
  3. Number of patients with <10% asymmetry in running biomechanical parameters

    Time frame: At 6 month post surgery

    Asymmetry <10% in biomechanical running parameters (stride length or stiffness coefficient of each lower limb)

Study contacts

Contact information is provided by the study sponsor or research team.

GREGORY MOREL, physio

CONTACT

[email protected]

(0)4 77 12 94 55 ext. +33

Thomas NERI, MD

CONTACT

[email protected]

(0)4 77 12 08 26 ext. +33

Sponsors and collaborators

Lead sponsor

Centre Hospitalier Universitaire de Saint Etienne

Other

Collaborators

  • Ministry of Health, France

Registry information

Official study title

Optimized Rehabilitation After Anterior Cruciate Ligament Reconstruction at the First Step of Return to Sport

Acronym: ORACL-Run

Important dates

Study start
2022
Primary completion
2028
Study completion
2029
First posted
Apr 12, 2022
Registry last updated
Apr 24, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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