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Enrolling By InvitationNCT06774157

Evaluation of the Efficacy of the ALLYANE Procedure in the Treatment of Central Motor Inhibition

Evaluation of the Efficacy of the ALLYANE Procedure in the Treatment of Central Motor Inhibition Immediately After Knee Sprain as an Adjunct to Conventional Treatment.

Status
Enrolling By Invitation
Phase
N/A
Study type
Interventional
Enrollment
120 (estimated)
Sponsor
Allyane · Industry
Sex
Female
Age
18 Years – 35 Years
Healthy volunteers
Not accepted

Summary

The goal of this clinical study is to determine the effectiveness of restoring muscle strength in the management of motor inhibition when complemented by the ALLYANE process (neuro-motor reprogramming) compared to a standard management approach. The main questions it aims to answer are: * Does the ALLYANE process lead to greater muscle strength gains compared to standard care? * Is there a functional benefit when standard management is complemented by the ALLYANE process? The investigators will compare the group receiving standard care complemented by ALLYANE to a group receiving only standard care to evaluate if the ALLYANE process provides additional effects. Participants will: * Undergo assessments of muscle strength. * Receive either standard management or standard management with ALLYANE. * Complete functional evaluations before and after treatment.

Detailed description

This study aims to evaluate the effectiveness of motor inhibition management using two different approaches: standard management alone and standard management supplemented by the ALLYANE neuro-motor reprogramming process. To ensure robust and reliable results, the study proposes enrolling a total of 120 patients, divided into two groups of 60 patients each.

Conditions

Interventions

TypeNameDescription
OTHERA session combining motor imagery and listening to low frequency soundsProspective study of the efficacy of the Allyane procedure after knee sprain
OTHERStandard management - Control groupActive extension (e.g. by lateral raising of the quadriceps, strengthening of the quadriceps) quadriceps)
OTHERStandard management - Control groupFlexor inhibition (e.g. massage, hamstring stretching)
OTHERStandard management - Control groupActive flexion (e.g. strengthening the flexors)

Timeline

Start date
2024-01-15
Primary completion
2026-12-20
Completion
2026-12-20
First posted
2025-01-14
Last updated
2025-03-07

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT06774157. Inclusion in this directory is not an endorsement.