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Clinical Trials in France / NCT03913962
Recruiting Not applicable

Health and Exercise Response in Children With Chronic and Auto-immune Pathologies

NCT03913962 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2019-05-02
Last updated
2019-05-08

Condition(s) studied

Juvenile Idiopathic ArthritisDiabetesInflammatory Bowel DiseaseCancer SurvivorAnorexia Nervosa

Investigational drug(s) / intervention(s)

indirect calorimetry

indirect calorimetry: Patients will be separated in different subgroups. Subgroups will be constituted according the disease status (i.e. active vs inactive) to assess the impact of the pathology on physical fitness and according to treatments to assess the effect of treatment on physical fitness.

Study summary

The aim of the present project is to assess the effects of the chronic diseases and their associated treatments chronic paediatric diseases (CPD), to further understand their impact on physical fitness for public health perspectives. This is an innovative approach in the treatment of chronic paediatric diseases . This project should yield results that help improving treatments for children and adolescents with chronic paediatric diseases throughout physical activity as therapy, reduced pain, fatigue and inflammation, and improvement in physical fitness and life quality. The originality and novelty of this project is to combine architectural, functional and metabolic components of skeletal muscle to further understand the impact of chronic paediatric diseases as a function of treatment, disease activity and maturation status (prepubertal, pubertal or post pubertal).

This study will aim at assessing muscular function (force production capacity and fatigability) in specific or ecologic situations so as to get information about muscle functioning on isolated muscle group (here knee extensors) or during whole body exercise. Moreover, results arising from muscle architecture or quality will allow understanding the decrease in strength or endurance reported in the literature. The data collected will allow us to further understand the impact of the disease on structural, functional and metabolic parameters. Finally, the understanding of these alterations will provide information enabling to establish recommendations in physical activity (PA) to reduce or even counter the effect of the chronic inflammation and prevent at long-term overweight and cardiovascular risks.

The long-term objective is to contribute establishing recommendations or guidelines for prescribing physical activity during medical therapy. Values obtained in pathological children will be compared to those of control children matched for gender and maturation.

Eligibility

Sex
ALL
Min age
6 Years
Max age
18 Years
Healthy volunteers
Accepted
Inclusion Criteria: * for patients: * Aged between 6 and 18-year-old * Male or female * Presenting a chronic pathology / having a treatment which is known to alter muscle mass and function, metabolism and body composition * Included in the active list of the hospital centre of Clermont-Ferrand * Free and informed consent of the holders of parental authority and the patient * Affiliated with the social security system for control: * Aged between 6 and 18-year-old * Male or female * Free and informed consent of the holders of parental authority and the patient * Affiliated with the social security system Exclusion Criteria: * for patients: * Treatment by systemic corticoids (\>1 week in the 30 days before test) * Contraindication to sport practice * Active infection for control: * Contraindication to sport practice * Chronic pathology susceptible to alter muscle mass and function, metabolism and body composition * Treatment susceptible to alter metabolism * Active infection

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Chu Clermont-Ferrand Clermont-Ferrand France Recruiting

More University Hospital, Clermont-Ferrand trials in France

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03913962 on ClinicalTrials.gov ↗ ← All trials in France