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New treatment option for Adolescent Idiopathic Scoliosis (AIS)
Official title Schroth and Pilates for Adolescent Idiopathic Scoliosis
ClinicalTrials.gov ID: NCT07702812
What this study is testing
- What it's testing
- The primary aim of this study is to investigate the effectiveness of Schroth training and the multidimensional effects of adding Pilates-based exercises to Schroth training in individuals with adolescent idiopathic scoliosis. Specifically, the study aims to evaluate the effects of Pilates-based exercises combined with Schroth training on lung capacity, trunk muscle strength, proprioception, trunk rotation, and posture.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 10 to 18
You may be able to join if
- Aged 10-18 years.
- Diagnosed with adolescent idiopathic scoliosis by a physician.
- Cobb angle between 10° and 45°.
- Willingness of both the participant and their parent/legal guardian to participate in the study.
- No additional rheumatologic, neurological, or orthopedic disorders.
You likely can't join if
- History of scoliosis or spinal surgery.
- Scoliosis secondary to neurological, congenital, or other non-idiopathic causes.
- Any contraindication to exercise.
- A spinal curve with an apex at T12-L1.
- Presence of cognitive impairment that would interfere with study participation or assessments.
- Current brace treatment. Participants who are eligible for bracing but have not been prescribed a brace by their physician or who decline brace...
See the full eligibility criteria
- Aged 10-18 years.
- Diagnosed with adolescent idiopathic scoliosis by a physician.
- Cobb angle between 10° and 45°.
- Willingness of both the participant and their parent/legal guardian to participate in the study.
- No additional rheumatologic, neurological, or orthopedic disorders.
- No scoliosis-specific treatment received within the previous 6 months.
- History of scoliosis or spinal surgery.
- Scoliosis secondary to neurological, congenital, or other non-idiopathic causes.
- Any contraindication to exercise.
- A spinal curve with an apex at T12-L1.
- Presence of cognitive impairment that would interfere with study participation or assessments.
- Current brace treatment. Participants who are eligible for bracing but have not been prescribed a brace by their physician or who decline brace treatment despite being eligible will remain eligible for inclusion.
The study team makes the final eligibility decision.
Where it's taking place
- Ankara, Turkey (Türkiye)
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 10 years to 18 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Ankara, Turkey (Türkiye). Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.