Effects of Resistance Exercises in Hereditary Sensory-Motor Neuropathy (Charcot-Marie-Tooth Disease)

NCT ID: NCT07152197

Last Updated: 2025-09-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

22 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-09-20

Study Completion Date

2026-09-20

Brief Summary

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The goal of this clinical trial is to compare the effects of an 8-week resistance exercise training program on skeletal muscle quality, functional capacity, and quality of life in young individuals aged 15 to 29 years, with and without Hereditary Sensorimotor Polyneuropathy (HSPN).

The main questions to answer are:

What is the effect of an 8-week resistance exercise training program on skeletal muscle quality, functional capacity, and quality of life in young individuals with and without HSPN?

Will the percentage of improvement after the program be greater in participants with HSPN compared to those without, due to greater baseline alterations?

Researchers will compare the resistance exercise training program with baseline conditions to determine its effectiveness in improving skeletal muscle quality, functional capacity, and quality of life.

Participants will undergo a supervised lower-limb resistance exercise program (3x/week) for 8 weeks. The intervention will include progressive loads from 60% to 80% of 1-Repetition Maximum (1RM), with exercises targeting the major lower limb muscle groups. All participants will complete pre- and post-intervention evaluations, including ultrasound assessment of muscle architecture, functional capacity tests, strength measurements, body composition analysis, and quality of life questionnaires.

Detailed Description

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Introduction: Hereditary sensorimotor polyneuropathy (HSPN), also known as Charcot-Marie-Tooth disease (CMT), is the most prevalent group of hereditary neuromuscular disorders. It is characterized by muscle distal weakness, muscle atrophy, sensory loss, balance impairments, skeletal deformities and, in some cases, respiratory dysfunction. These impairments lead to reduced muscle quality, functional capacity, and quality of life. Muscle quality encompasses both morphological and functional aspects of skeletal muscle, including muscle architecture, composition, and strength.

Resistance exercise training (RET) has been shown to improve strength, muscle morphology, and functional performance in various populations. However, there is limited evidence on its effectiveness in individuals with HSPN, particularly in young adults. No studies to date have compared the effects of lower-limb-focused RET on muscle quality, functional capacity, and quality of life in young adults with and without HSPN.

Objectives:

The primary objetive of this study will be to assess the change in muscle thickness and echogenicity as markers of muscle quality, evaluated through ultrasonography in the tibialis anterior muscles of the lower limbs of participants undergoing 8 weeks of resistance training

Secondary objectives include:

* Characterize muscle architecture through ultrasonographic evaluation (fascicle length, pennation angle, and muscle thickness).
* Assessing changes in body composition.
* Evaluating muscle regeneration biomarkers.
* Determining the impact on respiratory muscle strength and aerobic capacity
* Evaluate maximal handgrip strength
* Assess overall lower-limb strength
* Assess overall upper-limb strength
* Measure maximal voluntary isometric strength
* Evaluate functional ankle muscle strength
* Determine maximal lower-limb muscle strength
* Assess balance and gait performance
* Evaluate health-related quality of life (HRQoL)
* Analyze body composition
* Investigate muscle regeneration
* Monitor physical activity levels

Materials and Methods: This clinical trial will recruit 22 participants (n=11 with HSPN, n=11 without HSPN), aged 15-29 years. Participants will be assigned to an 8-week supervised lower-limb RET program, performed 3 times per week, with progressive loads from 60% to 80% of one-repetition maximum (1RM). Exercises will target the major lower limb muscle groups and include leg press, knee extension, knee flexion, and ankle dorsiflexion.

Assessments will be conducted pre- and post-intervention, including:

* Muscle architecture and composition via ultrasound (tibialis anterior thickness, fascicle length, pennation angle, echogenicity).
* Muscle strength tests (isometric voluntary contraction, 1RM, grip strength).
* Functional capacity tests (6-minute walk test, balance assessment).
* Body composition (bioimpedance, anthropometry).
* Health-related quality of life (SF-36 questionnaire).
* Blood markers for muscle regeneration (creatine kinase). All participants will maintain habitual diet and physical activity levels during the intervention.

Expected Results: It is hypothesized that 8 weeks of progressive RET will result in greater improvements in muscle quality, functional capacity, and quality of life compared to baseline in both groups, with greater relative improvements expected in participants with HSPN due to lower baseline values. Increases in tibialis anterior thickness and reductions in echogenicity are expected, along with improvements in muscle strength, aerobic capacity, and balance. No serious adverse events are anticipated.

Conditions

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Polyneuropathy Charcot Marie Tooth Disease (CMT)

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors
The expert evaluators of the pre- and post-intervention variables will be blinded.

Study Groups

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Charcot Marie Tooth (CMT Group)

Participants with Charcot-Marie-Tooth (CMT) will perform an 8-week supervised lower limb Progressive Resistance Exercise Training (RET) program, 3 times per week. Assessments will be conducted pre- and post-intervention to evaluate muscle quality, functional capacity, and quality of life.

Group Type EXPERIMENTAL

Progressive Resistance Exercise Training

Intervention Type OTHER

Progressive Resistance Exercise Training Supervised (RET) focusing on lower limbs. Warm-up (5 min cycling), followed by 5 sets of leg press, leg extension, leg curl, and weighted dorsiflexion. Cool-down with flexibility exercises. Load progression from 60% to 80% of 1Repetition Maximum across 8 weeks. Participants must complete ≥80% of sessions. Evaluators of pre- and post-intervention outcomes will be blinded.

CONTROL Group

Healthy participants (without Charcot Marie Tooth) will perform an 8-week supervised lower limb Progressive Resistance Exercise Training (RET) program, 3 times per week. Assessments will be conducted pre- and post-intervention to evaluate muscle quality, functional capacity, and quality of life.

Group Type ACTIVE_COMPARATOR

Progressive Resistance Exercise Training

Intervention Type OTHER

Progressive Resistance Exercise Training Supervised (RET) focusing on lower limbs. Warm-up (5 min cycling), followed by 5 sets of leg press, leg extension, leg curl, and weighted dorsiflexion. Cool-down with flexibility exercises. Load progression from 60% to 80% of 1Repetition Maximum across 8 weeks. Participants must complete ≥80% of sessions. Evaluators of pre- and post-intervention outcomes will be blinded.

Interventions

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Progressive Resistance Exercise Training

Progressive Resistance Exercise Training Supervised (RET) focusing on lower limbs. Warm-up (5 min cycling), followed by 5 sets of leg press, leg extension, leg curl, and weighted dorsiflexion. Cool-down with flexibility exercises. Load progression from 60% to 80% of 1Repetition Maximum across 8 weeks. Participants must complete ≥80% of sessions. Evaluators of pre- and post-intervention outcomes will be blinded.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Men or women between 15 and 29 years of age with a diagnosis of hereditary sensorimotor polyneuropathy (HSPN) in any of its subtypes, living in the community (for experimental group).
* Healthy men or women between 15 and 29 years of age living in the community (for control group).
* Having active ankle movement within a range from plantarflexion to at least 0° of ankle dorsiflexion, allowing for strength training.

Exclusion Criteria

* Osteoarticular or mobility impairments that prevent safe performance of resistance exercise training (e.g., ankle arthrodesis).
* Use of nutritional supplements that may affect skeletal muscle regulation (leucine, glutamine, casein, whey protein, fatty acids, creatine, among others).
* Untreated and/or uncontrolled chronic diseases or intellectual disability.
* History of surgery
* Participation in a resistance exercise training program within the past 6 months.
Minimum Eligible Age

15 Years

Maximum Eligible Age

29 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Universidad de La Frontera

OTHER

Sponsor Role lead

Responsible Party

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Fernando Javier Valenzuela Aedo

Clinical Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Temuco, Chile

Temuco, La Araucanía, Chile

Site Status RECRUITING

Universidad de La Frontera

Temuco, La Araucanía, Chile

Site Status ACTIVE_NOT_RECRUITING

Countries

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Chile

Central Contacts

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Fernando J Valenzuela, MSc

Role: CONTACT

+56950166328

Facility Contacts

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FERNANDO EXEQUIEL VALENZUELA NAVARRO

Role: primary

950166328

Related Links

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https://acsm.org/

The American College of Sports Medicine (ACSM) is a leading global organization dedicated to advancing and integrating scientific research, education, and practical applications in sports medicine, exercise science, and physical activity.

Other Identifiers

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054/25

Identifier Type: -

Identifier Source: org_study_id

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