Trials / Enrolling By Invitation
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
| Type | Name | Description |
|---|---|---|
| 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) |
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.