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Recruiting NCT07726043

Clinical Trial Evaluating the Impact of an Intensive Rehabilitation Program Combined With Tendon Vibratory Stimulation on Functional Balance in Individuals With Charcot-Marie-Tooth Disease Type 1A

No phase Interventional Charcot-Marie-Tooth Disease Type 1A

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Multidisciplinary rehabilitation program.
Who it may be relevant to
Registry conditions: Charcot-Marie-Tooth Disease Type 1A. Basic parameters: 18 years — 65 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Charcot-Marie-Tooth (CMT) disease is caused by a genetic abnormality involving the PMP22 gene, resulting in demyelination of the peripheral nerves. Demyelination leads to sensorimotor impairment and causes progressive muscle weakness and tendon contractures, initially affecting the lower limbs. Consequently, individuals with CMT experience balance impairments and gait disturbances, including ankle instability, foot drop, and postural instability, which lead to frequent falls and reduced quality of life. Currently, there is no disease-modifying treatment for CMT. Several rehabilitation approaches have been proposed, including endurance training and muscle strengthening programs, to improve independence in activities of daily living. However, rehabilitation practices for individuals with CMT remain poorly standardized, and there is still a lack of clearly defined rehabilitation protocols, despite broad agreement among healthcare professionals regarding their potential benefits. More recently, noninvasive focal tendon vibration has been investigated in several neurological disorders to improve sensory function, balance, and motor performance. Previous studies suggest that mechanical vibratory stimulation applied to the quadriceps tendon may induce sustained improvements in postural control and lower-limb muscle strength. The present study aims to evaluate a rehabilitation program combined with tendon vibratory stimulation. The objective is to compare the effectiveness of a short-term (2-week), intensive multidisciplinary rehabilitation program focused on balance with different types of focal tendon vibration, in order to better address balance impairments and their associated complications in individuals with Charcot-Marie-Tooth disease.

Detailed description

Charcot-Marie-Tooth (CMT) disease is the most common inherited peripheral neuropathy, with a prevalence ranging from 3.1 to 82.3 per 100,000 individuals. It is caused by genetic abnormalities affecting peripheral nerves. The most common form, accounting for approximately 60% of CMT cases, is Charcot-Marie-Tooth disease type 1A (CMT1A). CMT1A is characterized by a demyelinating neuropathy, autosomal dominant inheritance, and a mutation involving the PMP22 gene.

The first clinical signs of the disease typically appear before the age of 20 years and consist of a length-dependent sensorimotor impairment with distal predominance and diffuse areflexia. The disease primarily affects the lower limbs; upper limb involvement is variable and may develop after several years of disease progression. These impairments result in progressive distal muscle weakness associated with muscle atrophy, tendon contractures leading to pes cavus and claw toe deformities, and mild-to-moderate distal sensory impairment. These manifestations lead to major functional complaints among individuals with CMT, including balance disorders, gait disturbances related to ankle instability, foot clearance difficulties during the swing phase, and postural instability, resulting in frequent falls and impaired quality of life.

Currently, there is no disease-modifying treatment for CMT.

Assistive devices and lower-limb orthotic management may be prescribed. Surgical treatment may be considered in cases of severe and disabling musculoskeletal deformities.

Several rehabilitation approaches have been proposed, including endurance training and strengthening programs to improve independence in activities of daily living, as well as aerobic training programs aimed at improving functional capacity, aerobic capacity, muscle strength, and fatigue in individuals with CMT. The French National Diagnostic and Care Protocol (PNDS) for hereditary motor and sensory neuropathies associated with CMT highlights the lack of standardized rehabilitation practices and clearly defined protocols, despite a consensus among healthcare professionals regarding their potential benefits. Indeed, the literature includes only one randomized controlled trial, published in 2006, with a small sample size (n = 16), demonstrating improvements in balance, assessed using the Berg Balance Scale (BBS), following a two-week dynamic training program combining passive stretching, muscle strengthening, and standing balance exercises.

In addition, non-invasive focal tendon vibration has been proposed in several neurological disorders to improve sensory function, balance, and motor performance, particularly in individuals with diabetic peripheral neuropathy. Some studies suggest that mechanical vibratory stimulation applied to the quadriceps tendon may induce sustained improvements in postural control and lower-limb strength in women over 60 years of age.

In individuals with CMT, a pilot study involving 14 participants with CMT1A demonstrated improved balance performance on the Berg Balance Scale following three consecutive days of musculoskeletal vibration therapy applied to the quadriceps and triceps surae muscles.

In this context, we selected the Vibramoov device, a neurorehabilitation device that has already demonstrated clinical benefits in comparable studies involving other neurological disorders. Vibramoov delivers vibrations applied at the musculotendinous junction, thereby mechanically stimulating muscle spindles and reproducing the sensory signals associated with natural movement. This approach, already validated in other clinical settings, represents a promising strategy to improve balance and gait in individuals with CMT by integrating it into an intensive multidisciplinary rehabilitation program.

Therefore, it appears relevant to investigate a specific intensive multidisciplinary rehabilitation program combined with mechanical vibratory stimulation to improve functional balance and gait abilities in individuals with CMT.

Interventions

  • Other Multidisciplinary rehabilitation program
    2-week intensive multidisciplinary rehabilitation program including physical therapy, occupational therapy, and adapted physical activity sessions, followed by balance assessments and evaluation of neuropathy status.

Primary outcome measures

  • Berg Balance Scale [Time frame: Baseline, Week 3 , Week 7, Week 15]
Secondary outcome measures (12)
  • CMT Neuropathy Score [Time frame: Baseline, Week 3 , Week 7, Week 15]
  • Posturography [Time frame: Baseline, Week 3, Week 7, Week 15]
  • Timed Up and Go (TUG) test [Time frame: Baseline, Week 3, Week 7, Week 15]
  • Knee joint position sense assessment using electronic goniometers [Time frame: Baseline, Week 3, Week 7, Week 15]
  • Gait assessment [Time frame: Baseline, Week 3, Week 7, Week 15]
  • Walking speed [Time frame: Baseline, Week3, Week 7, Week 15]
  • Borg Rate of Perceived Extorsion (RPE) scale [Time frame: Baseline, Week 3, Week 7, Week 15]
  • Muscle strength assessment [Time frame: Baseline, Week 3, Week 7, Week 15]
  • Patient-Reported Outcome: R-ODS questionnaire [Time frame: Baseline, Week 3, Week 7, Week 15]
  • Patient-Reported Outcome: FSS Scale [Time frame: Baseline, Week 3, Week 7, Week 15]
  • Patient-Reported Outcome: QoL NMD v1.0 [Time frame: Baseline, Week 3, Week 7, Week 15]
  • Patient-reported Outcome: NRS Scale [Time frame: Baseline, Week 3, Week 7, Week 15]

Eligibility criteria

Inclusion criteria

  • Individuals with genetically confirmed Charcot-Marie-Tooth disease type 1A (CMT1A), characterized by PMP22 gene duplication on chromosome 17 (17p11.2).
  • Age between 18 and 65 years.
  • Overall Neuropathy Limitations Scale (ONLS) score between 2 and 3/7 for the lower limbs.
  • Affiliation with a social security/health insurance system.
  • Written informed consent voluntarily provided after receiving information regarding the study objectives, procedures, and potential risks.

Exclusion criteria

  • Comorbidities causing peripheral neuropathy (e.g., diabetes, renal failure, medication-induced neuropathy).
  • Balance or gait disorders due to another cause.
  • Individuals without a permanent residence.
  • Individuals deprived of liberty by judicial or administrative decision or under legal guardianship.
  • Individuals unable to understand the study objectives and procedures or unable to provide informed consent.
  • Individuals unable to complete all study procedures.
  • Previous use of the Vibramoov device.
  • Pregnant women or women planning to become pregnant during the study period.
  • Concurrent participation in another research study.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Quadruple blind
Primary purpose
Supportive care

Study locations

France · 1 center
  • IUR Valmante Sud — Marseille

Identifiers

NCT: NCT07726043 · 2024-A02577-40 · 2024-A02577-40

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗