LENGTH-FATIG: Neuromuscular Fatigue Aetiology Comparison Between Prepubertal Boys and Adults

Sponsor

University Hospital, Clermont-Ferrand (Other)

Overall Status

Completed

CT.gov ID

NCT03049241

Collaborator

Laboratoire des Adaptations Métaboliques à l'Exercice en conditions Physiologiques et Pathologiques (Other)

Enrollment

Location

9.2

Actual Duration (Months)

5.4

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

Potential factors involved in neuromuscular fatigue were classified into two categories: 1) central factors involving the central nervous system and neural pathways, and 2) peripheral factors occurring within the muscle beyond the neuromuscular junction. In adults, it has been shown that peripheral factors contribute to a large part of the fatigue induced by repeated maximal contractions. However in children, central factors could account for the development of fatigue to a greater extent. Force-generating capacity and musculotendinous stiffness could be two of the discriminatory factors accounting for the differences in the neuromuscular fatigue between children and adults.

Force production capacity and musculotendinous stiffness vary as function of muscle length. Naturally, they could differ depending on the muscle groups studied. The main aim of the present protocol is to compare the effect of knee extensors and ankle plantarflexors length on the development and aetiology of neuromuscular fatigue, in children and adults. The investigators formulated the hypotheses that at short muscle length force and low musculotendinous stiffness, differences in force between children and adults would be reduced. Thus neuromuscular fatigue development and aetiology would be similar between both groups. The results of the present protocol will allow to better understanding of the aetiology of neuromuscular fatigue in children and help improving training or rehabilitation programs.

Condition or Disease	Intervention/Treatment	Phase
Neuromuscular Fatigue	Other: neuromuscular fatigue

Detailed Description

The study of neuromuscular fatigue in children is a recently topic in the field of sport sciences. Such knowledge could improve the efficiency and security of training and rehabilitation in healthy children and children with diseases like obesity.

The LENGTH-FATIG study will provide knowledge about the peripheral and central mechanisms of the neuromuscular fatigue in children and adults. Fatigue will test for different muscle groups (knee extensors and ankle plantar flexors) at different muscle lengths (short, optimal and long).

During high-intensity exercise, prepubertal children are more resistant to fatigue than adults. Contributions of the central and peripheral components to the development of neuromuscular fatigue are also different between both populations. The reduced children's fatigue coud be particularly related to a lower peripheral (i.e. muscular) fatigue. This might be attributed to the fact that prepubertal children rely more on oxidative than anaerobic metabolism than adults during fatiguing exercise. On the other hand, nervous factors could also explain differences in fatigue between children and adults. However, this topic is scarcely documented and still controversial. To our knowledge, no study has still compared the aetiology of central fatigue (supra-spinal vs. spinal) between children and adults. Only the voluntary activation level had been studied in children, conventionally used to assess central fatigue. But this factor doesn't differentiate spinal and supra-spinal contributions to neuromuscular fatigue development.

The LENGTH-FATIG research project is a physiological and observational study comparing two age groups (adults and children). Subjects will have to perform three randomized fatigue protocols at three muscle lengths (short, optimal and long) with the knee extensors and the ankle plantar flexors.

Data will be analyzed using LabChart 7.3 Pro software (ADInstrument, New South Wales, Australia) and Statistica 8.0 software (StatSoft, Inc.) and significance will be accepted at a two-sided alpha level of p<.05. The normality and homogeneity of the variables will be checked respectively from a Shapiro-Wilk test and a Barlett test.

If normality and homogeneity of the variables are verified, absolute values of variables (Force, EMG, NIRS, etc.) will be compared using three factors (age x muscle length x muscle group) analyses of variance (ANOVA) with repeated measures. If analyses reveal a significant effect of any factor or interaction of factors, post-hoc Newman-Keuls tests will be performed to determine differences between the different conditions.

If, on the contrary, normality and homogeneity of the variables are not verified, the effects of muscle length, muscle group and age will be evaluated using a Friedman test. If the tests show significant effects, comparisons of the different conditions will be performed using Mann-Whitney and Wilcoxon tests.

Study Design

Study Type:

Observational

Actual Enrollment :

50 participants

Observational Model:

Other

Time Perspective:

Prospective

Official Title:

Neuromuscular Fatigue Aetiology Comparison Between Prepubertal Boys and Adults

Actual Study Start Date :

Feb 13, 2017

Actual Primary Completion Date :

Nov 20, 2017

Actual Study Completion Date :

Nov 20, 2017

Arms and Interventions

Arm	Intervention/Treatment
knee extensors	Other: neuromuscular fatigue The main aim of the present protocol is to compare the effect of knee extensors and ankle plantarflexors length on the development and aetiology of neuromuscular fatigue, in children and adults
ankle plantar	Other: neuromuscular fatigue The main aim of the present protocol is to compare the effect of knee extensors and ankle plantarflexors length on the development and aetiology of neuromuscular fatigue, in children and adults

Arm

Intervention/Treatment

knee extensors

Other: neuromuscular fatigue

The main aim of the present protocol is to compare the effect of knee extensors and ankle plantarflexors length on the development and aetiology of neuromuscular fatigue, in children and adults

ankle plantar

Other: neuromuscular fatigue

The main aim of the present protocol is to compare the effect of knee extensors and ankle plantarflexors length on the development and aetiology of neuromuscular fatigue, in children and adults

Outcome Measures

Primary Outcome Measures

Maximal torque of knee extensors [once a week during six weeks.]
ankle plantar flexors joint (in N.m) measured with a dynamometer. [once a week during six weeks.]

Secondary Outcome Measures

Doublet torque amplitude (100Hz, in N.m) evoked using magnetic nerve stimulation at rest [once a week during six weeks.]
Muscular tissue oxygenation (in μmol.L-1) measured at skin surface by Near-infrared spectroscopy. [once a week during six weeks]
Compound muscle action potential amplitude (i.e. M-wave ; in mV) evoked by supramaximal magnetic nerve stimulation and measured by surface Electromyography (EMG). [once a week during six weeks]
High frequency doublet (100Hz)/low frequency doublet (10Hz) ratio [once a week during six weeks]
fascicule length (mm) measured by B-mode real time ultrasound scanner. [once a week during six weeks]
pennation angle (degree) measured by B-mode real time ultrasound scanner. [once a week during six weeks]
Voluntary activation level (in %) assessed by using the twitch interpolation technique. [once a week during six weeks]
EMG signal Root mean square of EMG signal during isometric maximal voluntary contractions. [once a week during six weeks]
Hoffman reflex amplitude (i.e. H-reflex ; in mV) evoked by submaximal magnetic nerve stimulation measured by surface Electromyography (EMG). [once a week during six weeks]
Cerebral tissue oxygenation (in μmol.L-1) measured at skin surface by Near-infrared spectroscopy [once a week during six weeks]

Eligibility Criteria

Criteria

Ages Eligible for Study:

8 Years to 35 Years

Sexes Eligible for Study:

Male

Accepts Healthy Volunteers:

Yes

Inclusion Criteria:

Boys aged 8 to 11 years old, Tanner stages 1 to 3
Male aged 18 to 35 years old
Non-smoker
Moderate physical activity level (< 4h/week)
Covered by a social health insurance
Consent form signed by participants and/or legal guardians.

Exclusion Criteria:

Competitive training
Cardiac or pulmonary diseases
Epileptic seizures past history
Magnetic field contraindication (including cardiac valve, pacemaker, prosthesis material, ferro-magnetic foreign body, cochlear implant and ocular prosthesis material.