NCT07366996

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

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
0mo left

Started Feb 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

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

Study Progress93%
Feb 2026May 2026

First Submitted

Initial submission to the registry

January 17, 2026

Completed
9 days until next milestone

First Posted

Study publicly available on registry

January 26, 2026

Completed
6 days until next milestone

Study Start

First participant enrolled

February 1, 2026

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2026

Completed
14 days until next milestone

Study Completion

Last participant's last visit for all outcomes

May 15, 2026

Expected
Last Updated

January 26, 2026

Status Verified

January 1, 2026

Enrollment Period

3 months

First QC Date

January 17, 2026

Last Update Submit

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

EXPERIMENTAL

Fifteen adolescents will participate in one-hour Schroth treatment sessions, conducted three times per week in center under therapist supervision on non-consecutive days.

Other: Schroth treatment

Scientific Exercise Approach to Scoliosis (SEAS)

EXPERIMENTAL

The 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.

Other: Scientific Exercise Approach to Scoliosis (SEAS)

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.

Scientific Exercise Approach to Scoliosis (SEAS)

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.

Schroth treatment

Eligibility Criteria

Age13 Years - 18 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64)

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

Study Sites (1)

Faculty of Physical Therapy - Delta University for Science and Technology

Gamasa, Egypt

Location

Study Officials

  • Khaled Olama, PhD

    Professor, Cairo University

    STUDY CHAIR
  • Maya Galal Abd El Wahab, PhD

    Ass. Professor, Cairo University

    STUDY DIRECTOR

Central Study Contacts

Mina Reda Rezk Nada, M.Sc

CONTACT

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

Locations