- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05259956
Trial on Two Treatments for Adolescent Idiopathic Scoliosis
The Impact of "3+1" Multidimensional Therapeutic Exercises on the Progression of Adolescent Idiopathic Scoliosis
Study Overview
Status
Conditions
Detailed Description
Adolescent idiopathic scoliosis is the most common three-dimensional structural deformity of the spine among adolescence, the International Society on Scoliosis Orthopaedic and Rehabilitation Treatment recommend specific exercise therapy to delay the progression of scoliosis. Many specific exercise therapies are effective in reducing the angle of coronal scoliosis, but their efficiency in sagittal and axial deformities hasn't been convincing. Recent studies have found that the axial asymmetry of the pelvis may be involved in the pathogenesis of idiopathic scoliosis, but there is no clinical study on the treatment of scoliosis by correcting the axial torsion of the pelvis neither at home nor abroad. So in this study, "3 plus 1" multidimensional exercise therapy was applied to mild adolescent idiopathic scoliosis for the first time.
The present study is a single-center randomized controlled trial conducted at the department of rehabilitation medicine, Aerospace Center Hospital. The written Informed consent will be obtained from each patient and one of their parents before inclusion. Eligible subjects will be randomized by a 1:1 allocation ratio either to the experimental group, in which the "3 plus 1" multidimensional exercise therapy will be performed and pelvic correction technique was adopted to correct pelvic axial rotation, or the control group, in which they will receive the Schroth-based exercise therapy. Blinded assessments will be conducted at baseline and 6-month after the intervention, including the differences in three-dimensional structural parameters of pelvis and spine, such as the ratio of the iliac widths, SRS-22 questionnaire, etc, to compare the efficacy of two different groups in improving the three-dimensional balance of the spine and the quality of daily life in adolescent idiopathic scoliosis.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Beijing, China
- Zhang yafei
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- A diagnosis of adolescent idiopathic scoliosis; Age from 10 to 18 years; A Cobb angle of 10 to 25 degrees; All maturity levels (Risser sign of 0-5).
Exclusion Criteria:
- Non-idiopathic scoliosis, which is caused by a neuromuscular, neurological, congenital malformation, or trauma-related comorbidity; Having mental problems or other contraindications to exercise; Previous fractures, rheumatic diseases, or operation history of lower extremities; Previous or current brace or surgical treatments for scoliosis.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: "3 plus 1" multidimensional exercise therapy
The intervention consists of a Schroth-based exercise session and a manipulative therapy of pelvic asymmetry.
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The intervention is set to be delivered in a 90-minute exercise session, with a frequency of twice a week for five weeks.
The exercise consists of a one-hour Schroth-based exercise session and an additional 30-minute manipulative therapy of pelvic asymmetry.
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Active Comparator: Schroth based scoliosis specific exercise
The intervention consists of the Schroth-based exercise session.
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The intervention is set to be delivered in a one-hour Schroth-based exercise session, with the frequency of twice a week for five weeks.
The exercise consists of active auto-correction in 3D, stabilizing the corrected posture, and training in ADL.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Change From Baseline in Ratio of Iliac Widths at 24th week
Time Frame: baseline and at 24th week
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Rotation in the transverse plane of pelvic seen on a spinal standing full-length posteroanterior radiograph.
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baseline and at 24th week
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Change in Cobb Angle
Time Frame: baseline and at 24th week
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The largest coronal convex curve is measured by the Cobb method on a spinal standing full-length posteroanterior radiograph.
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baseline and at 24th week
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Change in Apical Vertebral Translation in Main Curves
Time Frame: baseline and at 24th week
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When an apical vertebra or disc is identified as the apex of the curve, the center of the vertebra or disc is identified by drawing a horizontal line through the vertebra or disc, apical translation of the disc is measured from the disc centroid to the center sacral vertical line (CSVL).
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baseline and at 24th week
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Change in Coronal Pelvic Tilt
Time Frame: baseline and at 24th week
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The vertical distance between the horizontal tangents of the highest point of the bilateral iliac crest.
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baseline and at 24th week
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Change in Apical Vertebral Rotation in Main curves
Time Frame: baseline and at 24th week
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The Nash and Moe method is used to determine vertebral rotation.
The apical vertebral body is divided into six equal segments longitudinally.
When both pedicles are in view, there is no vertebral rotation.
It is graded as "0".
When the pedicle in the concave side (the right side) starts disappearing, it is graded as "1".
When the pedicle disappears, it is graded as "2".
When the contralateral pedicle (pedicle in the convex side) is in the midline of the vertebra, it is graded as "3".
When it crosses the midline of the vertebra, it is graded as "4".
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baseline and at 24th week
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Change in Angle of Trunk Rotation
Time Frame: baseline and at 24th week
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The angle of trunk rotation will be measured with a Scoliometer.
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baseline and at 24th week
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Change in Scoliosis Research Society-22 Questionnaire
Time Frame: baseline and at 24th week
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The SRS-22 contains 22 questions covering 5 domains: function/activity 5 items; pain 5 items; self-perceived image 5 items; mental health 5 items; and satisfaction with treatment 2 items.
Each item is scored from 1 (worst) to 5 (best).
The sum of the 5 domains is 110.
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baseline and at 24th week
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Collaborators and Investigators
Investigators
- Study Director: Zhang Meng, Aerospace Centre Hospital
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
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Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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