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ENROLLING BY INVITATION
NCT06774157
NA

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

Sponsor: Allyane

View on ClinicalTrials.gov

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.

Official title: 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.

Key Details

Gender

FEMALE

Age Range

18 Years - 35 Years

Study Type

INTERVENTIONAL

Enrollment

120

Start Date

2024-01-15

Completion Date

2026-12-20

Last Updated

2025-03-07

Healthy Volunteers

No

Interventions

OTHER

A session combining motor imagery and listening to low frequency sounds

Prospective study of the efficacy of the Allyane procedure after knee sprain

OTHER

Standard management - Control group

Active extension (e.g. by lateral raising of the quadriceps, strengthening of the quadriceps) quadriceps)

OTHER

Standard management - Control group

Flexor inhibition (e.g. massage, hamstring stretching)

OTHER

Standard management - Control group

Active flexion (e.g. strengthening the flexors)

Locations (1)

Centre Expert du Mouvement

Lyon, France