- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06500806
Impact of Long-Term Schroth Exercises on Scoliosis Severity and Quality of Life in Braced AIS Individuals
The Effect of a Long-Term Schroth Exercise Program on the Severity of Scoliosis and Quality of Life in Adolescents With Adolescent Idiopathic Scoliosis Wearing a Brace: A Randomized Controlled Clinical Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Background: Adolescent Idiopathic Scoliosis (AIS) affects individuals aged 10 to 18 and is characterized by spinal deformity in the frontal plane, three-dimensional distortion of the spine, and vertebral rotation. Exercises based on the Schroth method, along with the use of a brace, have been shown to reduce the Cobb angle and may prevent further spinal deformity.
Objective: This clinical study aims to investigate the impact of a 12-month supervised Schroth exercise program on the severity of scoliosis and the quality of life in adolescents diagnosed with AIS.
Method: In this study, 80 adolescents aged 10 to 17 with AIS who are prescribed a brace are divided into two groups: an intervention group and a control group. The intervention group participates in a supervised Schroth exercise regimen three times weekly for a year, in addition to wearing a brace. The control group uses only the brace. Measurements include the Cobb angle of the main curve, the sum of the curves via Surgimap 2.3.2.1 software, the Angle Trunk Rotation (ATR) with a scoliometer, and quality of life assessed through the SRS-22 questionnaire. These assessments are conducted at the start, after one year (12th month), and six months post-intervention (18th month). The data are analyzed using Multivariate Analysis of Covariance (MANCOVA), with statistical significance set at p < 0.05.
Expected Results: Previous studies indicate that Schroth exercises can reduce the Cobb angle and ATR in adolescents with AIS and slow the progression of spinal deformity. However, few studies have investigated the effects of Schroth exercises for periods longer than six months. It is anticipated that incorporating Schroth exercises into a 12-month brace treatment program will significantly improve both the severity of scoliosis and the quality of life for the participants.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Sindos Thessaloníki
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Thessaloníki, Sindos Thessaloníki, Greece, 57 400
- Department of Physiotherapy, Faculty of Health Sciences International Hellenic University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Diagnosed with Adolescent Idiopathic Scoliosis (AIS)
- Aged 10 to 17 years, inclusive of both genders
- Cobb angle between 10° and 45°
- Risser grade between 0 and 3
- Prescribed a scoliosis brace
- Written consent from their legal guardian for participation
- Ability to attend Schroth exercise sessions for one year
Exclusion Criteria:
- Any contraindication for exercise
- Scheduled surgery for scoliosis treatment
- Diagnosed intellectual disabilities (e.g., intellectual disability, autism)
- Diagnosed neurological or rheumatic conditions
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: Scroth and brace Group
Participants allocated to this group will receive bracing and Schroth exercises for 12 months
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Participants in this group will wear a brace and follow a 12-month Schroth exercise program three times a week.
Sessions will be supervised by a physiotherapist and last 60 minutes, using equipment like foam blocks, exercise balls, and rods.
Exercise intensity will gradually increase based on progress.
The individualized Schroth exercises will aim to correct spinal deformity and include elongation, rotational correction, stretches, strengthening, and breathing exercises.
These exercises will help patients maintain proper posture in daily activities and will be adapted to each participant's abilities, with varying difficulty and positions.
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Active Comparator: Brace group
Participants in this group will follow brace treatment.
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Participants in this group will follow only the brace treatment
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Changes in Cobb ankle
Time Frame: Pre-treatment, months: 12, 18
|
An independent orthopedic physician will measure the Cobb angle using Surgimap 2.3.2.1 software.
For each assessment, participants will undergo a radiological examination with a full spinal X-ray taken from an anteroposterior view while standing.
The study will evaluate the Cobb angle of the primary curvature (the largest curve) as well as the total sum of the Cobb angles of all identified curves.
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Pre-treatment, months: 12, 18
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Changes in maximum Ankle Trunk Rotation
Time Frame: Pre-treatment, months: 12, 18
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The ATR (Angle of Trunk Rotation) will be measured using a scoliometer.
For the ATR measurement, each participant will stand with their feet together in an upright position and perform a forward bend (Adam's forward bend test) until their back is parallel to the ground.
The scoliometer will then be placed vertically along the spine at the level where the rib hump appears.
In this study, the maximum ATR (ATR maximum) will be recorded.
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Pre-treatment, months: 12, 18
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Changes in quality of life with SRS - 22 questionnaire
Time Frame: Pre-treatment, months: 12, 18
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Participants' quality of life will be evaluated using the Scoliosis Research Society 22 (SRS-22) questionnaire.
The SRS-22 is the standard tool for assessing the quality of life in individuals with scoliosis, comprising 22 questions across five categories: functionality (5 questions), pain (5 questions), self-image (5 questions), mental health (5 questions), and treatment satisfaction (2 questions).
Responses are rated on a Likert scale from 1 to 5. The overall score is determined by averaging the subcategory scores, ranging from 1 (lowest) to 5 (highest), with higher scores indicating better quality of life.
This study will use the Greek version of the questionnaire.
The total SRS-22 score will be used to measure the quality of life.
The Greek version has been shown to have high reliability and validity compared to the 36-Item Short Form Survey (SF-36).
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Pre-treatment, months: 12, 18
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Collaborators and Investigators
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
- EC-09/2022
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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