Three-Dimensional Correction Methods for Idiopathic Scoliosis in Adolescent
1 other identifier
interventional
30
1 country
1
Brief Summary
This study aims to compare the effectiveness of "Schroth method" and "Scientific Exercise Approach to Scoliosis" for correcting idiopathic scoliosis in adolescents.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Feb 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 17, 2026
CompletedFirst Posted
Study publicly available on registry
January 26, 2026
CompletedStudy Start
First participant enrolled
February 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
May 15, 2026
ExpectedJanuary 26, 2026
January 1, 2026
3 months
January 17, 2026
January 17, 2026
Conditions
Outcome Measures
Primary Outcomes (2)
Cobb Angle
It will be assessed using standard standing posteroanterior spinal radiographs and will be measured before and after the intervention period. This outcome measure will be used to quantify the magnitude of the lateral spinal curvature and to evaluate changes in spinal alignment, allowing determination of the degree of curve correction or progression following the intervention.
12 weeks
Angle of Trunk Rotation (ATR)
It will be measured using a scoliometer during the Adam's forward bend test and will be assessed before and after the intervention period. This outcome measure will be used to evaluate the degree of rotational trunk deformity, reflecting the axial component of the three-dimensional spinal deformity in scoliosis.
12 weeks
Secondary Outcomes (2)
Risser Sign
12 weeks
Health-Related Quality of Life (HRQOL)
12 weeks
Study Arms (2)
Schroth treatment
EXPERIMENTALFifteen adolescents will participate in one-hour Schroth treatment sessions, conducted three times per week in center under therapist supervision on non-consecutive days.
Scientific Exercise Approach to Scoliosis (SEAS)
EXPERIMENTALThe home program will consist of fifteen adolescents coming to the center once a month for Scientific Exercise Approach to Scoliosis (SEAS) treatment sessions, each lasting one hour. These sessions will be conducted three days per week, one hour, at home on non-consecutive days.
Interventions
The SEAS exercise program emphasizes active self-correction, core stability, and postural control during functional movements. Key exercises include pelvic tilts, seated forward bends, standing side bends, supine marching, bird-dog, heel slides, chest openers, and supine knee-to-chest stretches, all performed with self-correction to maintain neutral spinal alignment, improve muscular control, flexibility, and long-term postural stability.
The exercise program targets three-dimensional spinal correction and includes Schroth breathing for rib cage expansion, pelvic tilts for pelvic alignment, side-shift exercises for lateral correction, rotational angular breathing for derotation, seated rotational stretches for lumbar flexibility, trunk elongation with resistance for postural strength, hanging stretches for spinal decompression, and arm-leg lifts to enhance core stability and coordination.
Eligibility Criteria
You may qualify if:
- Teenagers diagnosed with typical idiopathic scoliosis.
- Teenagers aged 13 to 18 years
- Both genders will be included.
- Participants with a Cobb angle ranging from 10° to 25°, as determined by radiographic analysis.
- Participants with Risser sign of 2 to 3, indicating incomplete skeletal maturity.
- Participants must be able to understand and follow instructions, ensuring effective participation in the treatment protocol.
You may not qualify if:
- Adolescents with significant visual or auditory impairments that could interfere with the ability to participate in or benefit from the rehabilitation programs.
- Adolescents with cognitive, mental, or psychological disorders that hinder understanding or following the instructions necessary for the treatment protocol.
- Adolescents who have previously undergone spinal surgery or any surgical interventions related to scoliosis or other spinal conditions.
- Adolescents with non-idiopathic scoliosis or scoliosis secondary to other underlying conditions (e.g., neuromuscular, congenital, or syndromic scoliosis).
- Adolescents with fixed spinal deformities that are not amenable to correction through non-surgical 3D approach.
- Adolescents with concurrent musculoskeletal conditions that could interfere with the treatment or assessment of scoliosis (e.g., significant hip or knee deformities).
- Adolescents currently participating in other clinical trials or receiving treatments that might confound the study results.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Cairo Universitylead
Study Sites (1)
Faculty of Physical Therapy - Delta University for Science and Technology
Gamasa, Egypt
Study Officials
- STUDY CHAIR
Khaled Olama, PhD
Professor, Cairo University
- STUDY DIRECTOR
Maya Galal Abd El Wahab, PhD
Ass. Professor, Cairo University
Central Study Contacts
Maya Galal Abd El Wahab, PhD
CONTACT
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
January 17, 2026
First Posted
January 26, 2026
Study Start
February 1, 2026
Primary Completion
May 1, 2026
Study Completion (Estimated)
May 15, 2026
Last Updated
January 26, 2026
Record last verified: 2026-01