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Postural Re-education for Adolescent Scoliosis (RCT-RPG Trial)
N/A
Recruiting
Led By Carole Fortin, PhD
Research Sponsored by St. Justine's Hospital
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
ability to travel weekly to attend GPR intervention
aged between 10 and 16 years old
Must not have
patients who are planned for surgery
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6, 12 and 24 months
Awards & highlights
No Placebo-Only Group
Summary
This trial aims to see if GPR, a type of physical therapy focusing on posture and muscle exercises, can help adolescents with scoliosis. The goal is to improve their spine alignment, reduce pain, and enhance their overall physical health.
Who is the study for?
This trial is for adolescents aged 10-16 with mild to moderate scoliosis (Cobb angle between 15º and 45º) who are still growing (Risser sign ≤3) and can travel weekly for treatment. It's not for those planning surgery, already wearing a brace for three months, or with conditions other than Adolescent Idiopathic Scoliosis.
What is being tested?
The study tests if Global Postural Re-education (GPR), involving special exercises and posture training, can help manage scoliosis better than standard care alone. Participants will be randomly assigned to receive either GPR plus standard care or just standard care over a period of up to one year.
What are the potential side effects?
While the trial doesn't list specific side effects, physiotherapy interventions like GPR may cause temporary muscle soreness or fatigue. The risk of serious side effects is generally low compared to medication-based treatments.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I can travel weekly for the treatment.
Select...
I am between 10 and 16 years old.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I am scheduled for surgery.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 6, 12 and 24 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6, 12 and 24 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Change in Cobb angle of at least 5 degrees
Secondary study objectives
Back pain on the Numerical Pain Rating Scale
Diaphragm excursion
Forced vital capacity
+3 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: GPR groupExperimental Treatment1 Intervention
GPR interventions added to standard care (observation or brace)
Group II: Standard care groupActive Control1 Intervention
Observation or brace plus conventional physiotherapy exercises on video
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The most common treatments for Adolescent Idiopathic Scoliosis (AIS) include exercise-based interventions like Global Postural Reeducation (GPR), which focus on improving posture, muscle function, and spinal alignment. GPR involves individualized sessions that target postural correction and muscle strengthening, aiming to prevent scoliosis progression and improve overall physical health and quality of life.
These treatments are essential for AIS patients as they can reduce the curvature of the spine, alleviate back pain, and enhance respiratory function, thereby improving daily functioning and long-term outcomes.
Effect of Schroth exercises on curve characteristics and clinical outcomes in adolescent idiopathic scoliosis: protocol for a multicentre randomised controlled trial.
Effect of Schroth exercises on curve characteristics and clinical outcomes in adolescent idiopathic scoliosis: protocol for a multicentre randomised controlled trial.
Find a Location
Who is running the clinical trial?
CHU de QuébecUNKNOWN
1 Previous Clinical Trials
88 Total Patients Enrolled
St. Justine's HospitalLead Sponsor
200 Previous Clinical Trials
85,696 Total Patients Enrolled
Laval UniversityOTHER
430 Previous Clinical Trials
178,251 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am scheduled for surgery.I can travel weekly for the treatment.I am between 10 and 16 years old.I have undergone surgery.My diagnosis is not AIS.The curve in your spine is between 15 and 45 degrees, as measured by the Cobb angle.Your bones are still growing and have not fully developed yet, which is indicated by a Risser sign of 3 or less.
Research Study Groups:
This trial has the following groups:- Group 1: Standard care group
- Group 2: GPR group
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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