The Impact of Superimposed Vibration on the Recovery of Muscle Strength and Function Following Anterior Cruciate Ligament Surgery

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-45
SponsorCentre orthopédique de Dracy-le-Fort

About this trial

Restoring muscle strength following knee ligament reconstruction (of the anterior cruciate ligament, ACL) is a major challenge for the functional success of rehabilitation. Despite advances in rehabilitation protocols, many patients still experience persistent strength deficits several months after surgery. Current rehabilitation strategies rely primarily on neuromuscular training programs aimed at restoring maximum strength and joint range of motion. However, these approaches exhibit significant interindividual variability and do not always fully resolve persistent muscle inhibition. In this context, local vibration appears to be a promising tool. This project aims to evaluate the benefits of repeated application of local vibration superimposed on muscle strengthening exercises (recovery of quadriceps strength, single-leg balance, quadriceps power, perception of effort and pain, knee range of motion) performed during the first six weeks of post-ligamentoplasty rehabilitation. The underlying hypothesis is that the addition of sensory stimulation via vibration, superimposed on rehabilitation exercises, could facilitate muscle activation and, ultimately, accelerate the functional recovery of the quadriceps.The expected results could help validate the use of this approach as a standardized tool within post-ACL rehabilitation protocols, by promoting faster muscle recovery and reducing the duration of functional disability.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Men or women who have undergone anterior cruciate ligament reconstruction (using the Kenneth Jones method or a hamstring graft) on the right or left leg

Be between the ages of 18 and 45

Be enrolled in or eligible for a social security program

Have signed an informed consent form

Disqualifiers

Patients who have previously undergone anterior cruciate ligament reconstruction

Patients not currently under care at the Dracy-le-Fort Orthopedic Center

Patients with chronic sensorimotor disorders

Patients who have previously undergone ligament reconstruction on the knee currently being operated on

Trial design

Design model

Parallel

Treatments tested in this trial

  • Vibramoov, Techno Concept, Mane, France

    Device

    Local vibration superimposed on muscle contraction (SLV) is delivered using a dedicated device (Vibramoov, Techno Concept, Mane, France), which bears the CE mark (European Medical Devices Directive, Class IIa) and is designed and manufactured in accordance with ISO 13485: 2016.

  • No device

    Other intervention

    No device applied on quadriceps

Treatment groups

62 Participants
are divided into 2 treatment groups
Group A: Traditional rehabilitation without vibrationSham comparator 1 intervention
Group B: Application of localized vibration during certain muscle-strengthening exercisesExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Assessment of Quadriceps Strength Recovery During Postoperative Rehabilitation Following Anterior Cruciate Ligament Reconstruction, With or Without Local Vibration Superimposed on Muscle Strengthening Exercises

Measurement of changes in strength, with or without vibrations applied to the quadriceps during rehabilitation sessions. Quadriceps strenght will be measured by the maximum voluntary isometric contraction (MVIC): maximum force (kg) while seated. A quadriceps warm-up will begin with progressive isometric contractions, consisting of ten knee-extension contractions of the injured leg, ranging from light to strong intensity depending on the patient's perception. Following this, the patient will perform two 5-second maximal voluntary isometric contractions (MVICs) in extension, separated by 1-minute recovery periods, to measure quadriceps strength.

Time frame
Before surgery and after 6 weeks of rehabilitation

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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