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Clinical Trials in Canada / NCT04568759
Active, not recruiting Not applicable

Effect of a Postural Re-education Intervention Compared to Standard Care on Scoliosis Progression in Adolescent

NCT04568759 · tracked via the Priya Life Science Canada tracker
Phase
Not applicable
Started
2021-08-15
Last updated
2024-12-16

Condition(s) studied

Adolescent Idiopathic Scoliosis

Investigational drug(s) / intervention(s)

Global postural re-education

Global postural re-education: GPR consists of active treatment posture and sensorimotor control exercises to regain back muscle symmetry and correct posture in daily activities

Study summary

The aim of this project is to verify the effect of the global postural reeducation (GPR) intervention used in physiotherapy on scoliosis progression (scoliosis angle), back pain, quality of life, respiratory function, trunk posture and trunk muscle functioning and walking endurance. To do so, we will recruit 144 participants at three scoliosis specialized Centers. Participants will be randomly allocated to the standard of care (SC) group (observation or brace plus home video of exercises for 12 months) or to the GPR group (SC plus individual sessions once a week for 6 months and individual sessions alternating with telerehabilitation sessions once per two weeks between 6 and 12 months). At initial, 6, 12- and 24-months evaluation, participants will have x-ray, complete self-report questionnaires to document back pain and quality of life. Thereafter, measurement of trunk posture, electromyography activity of the back muscles, excursion of the diaphragm muscle using echography and respiratory function as well as distance covered using the 6-minute walk test for walking endurance will be done. We believe that GPR intervention may prevent scoliosis progression and improve physical health and quality of life in adolescence.

Eligibility

Sex
ALL
Min age
10 Years
Max age
16 Years
Healthy volunteers
No
Inclusion Criteria: * aged between 10 and 16 years old, * Cobb angle between 15º and 45º, * Risser sign ≤3 (skeletal growth incomplete), * with a risk of progression index \> 1.3, * having recent x-rays (4-6 weeks), * ability to travel weekly to attend GPR intervention Exclusion Criteria: * patients with diagnosis other than AIS, * patients who are planned for surgery, * have had surgery, * worn a brace for at least three months prior to GPR intervention

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
CHU Sainte-Justine Montreal Quebec
Centre interdisciplinaire de recherche en réadaptation et intégration sociale/Université Laval Québec Canada

More St. Justine's Hospital trials in Canada

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 NCT04568759 on ClinicalTrials.gov ↗ ← All trials in Canada