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L'essai clinique NCT01761305 (CONTRAIS) pour Scoliose idiopathique est actif, pas en recrutement. Consultez la vue en carte du Radar des Essais Cliniques et les outils de découverte par IA pour tous les détails, ou posez vos questions ici.
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Trial on Three Treatments for Scoliosis (CONTRAIS)

Actif, pas en recrutement
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L'étude clinique NCT01761305 (CONTRAIS) est un essai interventionnel pour Scoliose idiopathique. Son statut actuel est : actif, pas en recrutement. L'étude a débuté le 1 janvier 2013 et vise à recruter 135 participants. Dirigé par l'Institut Karolinska, l'essai devrait être terminé d'ici le 1 décembre 2030. Les données du site ClinicalTrials.gov ont été mises à jour pour la dernière fois le 21 février 2025.
Résumé succinct
Idiopathic scoliosis is a three-dimensional structural deformity of the spine that occurs in children. Recent reviews on bracing and exercise treatment have provided some evidence for effect of these interventions. The purpose of this study is to compare the effectiveness of night time bracing, scoliosis specific exercises and physical activity prescription in adolescents with idiopathic scoliosis.
Description détaillée
Today, bracing is used to prevent progression of idiopathic scoliosis in children.

The evidence for bracing and physical activity for treatment of idiopathic scoliosis is poor. Only one low quality study has compared bracing with physical exercise, showing no statistical differences in the reduction or progression of scoliosis curves between the groups. To draw valid conclusions about the effectiveness of postural specific physical exercise and brace therapeutic interventions compared to a self mediated activity exercise group, a randomized controlled trial research design will be used.

Preliminary data suggests that approximately 8 hours of night-time bracing with an over-corrective brace is as effective as bracing during 23 hours per day. Night-time bracing is attractive since you wear the brace a limited amount of time.

Several theories propose that during the adolescent period of skeletal growth, bone deformation may occur due to a combination of asymetrical growth plate activity, vertebral body weakness or an imbalance of muscle forces and joint flexibility. An association between low bone mineral density and idiopathic scoliosis has been reported in the literature. Adequate physical activity levels is a requirement for normal growth and development during childhood and adolescents. It is well documented that physical exercise is associated with improvements in not only muscle strength, aerobic fitness and motor development but also bone density which may help decrease the risk of osteopenic related bone deformation.

Patients included in the study will be randomized to one of three groups. Each of the three groups will receive a physical activity prescription according to World Health Organisation recommendations. One group will additionally wear a hyper-corrective night-time brace. One group will additionally perform postural scoliosis-specific exercises. Patients not wanting to be randomized to the alternative treatments in the clinical trial will receive bracing which is the current standard treatment offered.

The purpose of the study is to compare the risk of curve progression in the different groups. Curve progression is measured on x-rays. Participation in the study will last until the curve has progressed, or until cessation of skeletal growth. Participants with braces will be instructed to wear the brace 8 hours per night. Participants receiving scoliosis specific training will receive 3x90 minute physiotherapist guided sessions with an additional session provided every 6 months for the entirety of the study. All participants will be recommended to be physically active at least 60 minutes per day.

Titre officiel

CONTRAIS: CONservative TReatment for Adolescent Idiopathic Scoliosis. A Randomised Controlled Trial

Conditions
Scoliose idiopathique
Publications
Articles scientifiques et travaux de recherche publiés sur cet essai clinique:
Autres identifiants de l'essai
  • CONTRAIS
  • PG-AA-2012-12-19
Numéro NCT
Date de début (réel)
2013-01
Dernière mise à jour publiée
2025-02-21
Date de fin (estimée)
2030-12
Inscription (estimée)
135
Type d'essai
Interventionnel
PHASE
N/A
Statut
Actif, pas en recrutement
Mots clés
Idiopathic scoliosis
Brace
Scoliosis specific exercise
Physical activity
Objectif principal
Traitement
Plan d'attribution
Randomisé
Modèle d'intervention
Parallèle
Masquage
Simple aveugle
Bras / Interventions
Groupe de participants/BrasIntervention/Traitement
ExpérimentalBrace
Hypercorrective night-time brace worn 8 hours per night. A prescription of general physical activity will be provided at a dose of 60 minutes per day. Instructions regarding physical activity will be delivered during a one hour session.
Hypercorrective Night-time Brace
Hypercorrective night-time brace worn 8 hours per night. Patients are encouraged to also continue with non-specific self-mediated physical activities of moderate intensity at least 60 minutes daily, for the entirety of the study. Reinforcement of the assigned intervention will be performed in conjunction with reassessment every 6 months. A training diary will be implemented to follow and motivate the patient's training behaviour.
ExpérimentalScoliosis specific exercises.
Scoliosis specific exercises. The intervention will be delivered in 3 x 90 minute sessions, once per month during the first 3 months. An additional session will be provided every 6 months for the entirety of the study. A prescription of general physical activity will be provided at a dose of 60 minutes per day.
Scoliosis Specific Exercises.
The intervention will be delivered in 3 x 90 minute sessions, once per month during the first 3 months. Goals are directed towards active self-correction and postural control, spinal stability, aerobic functioning and development of a positive body image. Additional postural specific exercises including self-mediated hyper-corrective exercises are to be performed with moderate intensity at least for 30 minutes at least 2-3 times per week. Other physical activities to fulfill the general recommended quota of more than 60 minutes moderate intensity physical activity per day are recommended. Reinforcement of the intervention will be performed in conjunction with reassessment every 6 months. A training diary will be implemented to follow and motivate the patient's training behaviour.
Comparateur actifSelf-mediated physical activity.
A prescription of general physical activity will be provided at a dose of 60 minutes per day. Instructions will be delivered during a 1 hour session.
Self-mediated Physical Activity.
Instructions for self-mediated physical activity will be delivered during a 1 hour session. Patients are encouraged to perform self-mediated physical activities of moderate intensity at least 60 minutes daily, for the entirety of the study. Reinforcement of the assigned intervention will be performed in conjunction with reassessment every 6 months. A training diary will be implemented to follow and motivate the patient's training behaviour.
Critère principal d'évaluation
Critères d'évaluationDescription de critèresPériode
Radiological progression of scoliosis
Progression of the Cobb angle more than 6 degrees, compared to the primary x-ray, seen on two consecutive spinal standing x-rays.
Measured every 6 months, for an expected average of three years
Critère secondaire d'évaluation
Critères d'évaluationDescription de critèresPériode
Quality of life assessed with questionnaire instruments
Quality of life measured with validated questionnaires such as Euroqol (EQ5D-Y), Scoliosis Research Society outcomes questionnaire 22r (SRS22r), International Physical Activity Questionnaire (IPAQ) and the Walter Reed Visual Assessment Scale.
Measured every 6 months, for an expected average of three years
Curve severity at end of study.
Curve severity measured as Cobb angle at end of study.
Measured at end of study, expected at an average of three years after study inclusion
Health economic evaluations; actual cost for a treatment
Actual analysis of direct costs, and estimations of indirect costs.
Measured at end of study, expected an average of three years after study inclusion
Neuroaxial abnormalities and risk of curve progression
Analysis of prevalence of neuroaxial abnormalities and any risk of scoliosis curve progression
Analysed when magnetic resonance images are available and all participants has arrived to the primary endpoint of the study
Curve severity comparing night time brace and full time brace
Curve severity measured as Cobb angle after randomization to night time brace, or after refraining randomization and receiving a full time brace
From brace initiation until skeletal maturity (estimated to about 3 years after inclusion), and 2, 5 and 10 years after skeletal maturity
Critères d'éligibilité

Âges éligibles
Enfant
Âge minimum
9 Years
Sexes éligibles
Tous
  • Diagnosis of idiopathic scoliosis
  • Skeletally immature with estimated remaining growth for at least one year.
  • Not more than one year after menarche
  • Primary Cobb angle between 25 and 40 degrees.
  • Curve apex T7 or caudal

  • Scoliosis with a possible non-idiopathic ethiology. Patients will be excluded from the study if the pathogenesis of the scoliosis is not idiopathic, but due to a neuromuscular, neurological, congenital malformation or trauma related comorbidity.
  • Previous brace or surgical treatment for scoliosis.
Karolinska Institutet logoInstitut Karolinska
  • 🏥Karolinska University Hospital
  • 🏛️Region Stockholm
  • 🔬The Swedish Research Council
  • 🏥University Hospital, Linkoeping
Partie responsable de l'essai
Paul Gerdhem, Investigateur principal, MD, PhD, Professor, Karolinska Institutet
Aucune donnée de contact disponible
7 Centres de l'essai dans 1 pays
Mälarsjukhuset / Eskilstuna hospital, Eskilstuna, 63188, Sweden
Ryhov Hospital, Jönköping, 55185, Sweden
Linköping University, Linköping University Hospital, Linköping, 58183, Sweden
Karolinska University Hospital, Stockholm, 14186, Sweden
Sundsvall Hospital, Sundsvall, 85186, Sweden
Umeå University, Norrland University Hospital, Umeå, 90185, Sweden
Västerås Hospital, Västerås, 72189, Sweden