NCT07363226

Brief Summary

This study aims to compare the effectiveness of core stabilization exercises versus traditional rehabilitation exercises in adolescents with idiopathic scoliosis. Participants are assigned to one of two intervention groups: a core stabilization exercise program or a traditional rehabilitation program. The study evaluates the impact of both interventions on spinal stability, posture, and functional outcomes. The results of this study may help identify more effective rehabilitation approaches for managing adolescent idiopathic scoliosis.

Trial Health

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Trial Health Score

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

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
7mo 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 Progress32%
Feb 2026Dec 2026

First Submitted

Initial submission to the registry

January 16, 2026

Completed
7 days until next milestone

First Posted

Study publicly available on registry

January 23, 2026

Completed
9 days until next milestone

Study Start

First participant enrolled

February 1, 2026

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2026

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2026

Last Updated

January 27, 2026

Status Verified

January 1, 2026

Enrollment Period

9 months

First QC Date

January 16, 2026

Last Update Submit

January 24, 2026

Conditions

Adolescence Idiopathic ScoliosisCore Stabilization ExerciseTraditional RehabilitationAdolescents

Outcome Measures

Primary Outcomes (1)

  • Change in Cobb's Angle

    Cobb's angle measured using the DIERS Formetric 4D spinal analysis system in static mode

    Baseline and 12 weeks

Secondary Outcomes (3)

  • 1. Maximum Axial Vertebral Rotation (Max AVR)

    Baseline and 12 weeks

  • Pelvic Obliquity

    Baseline and 12 weeks

  • Quality of Life (QoL)

    Baseline and 12 weeks

Study Arms (2)

core stabilization exercises group

EXPERIMENTAL

A supervised core stabilization exercise program targeting deep and global trunk musculature including the transversus abdominis, multifidus, pelvic floor, diaphragm, rectus abdominis, erector spinae, and oblique muscles. The program was delivered three times per week for 12 weeks, with each session lasting 45 minutes. Exercises were progressively advanced from static to dynamic tasks according to participant tolerance and performance.

Behavioral: Core stabilization Exercises program

Traditional Rehabilitation Exercise Program

EXPERIMENTAL

A supervised traditional physiotherapy program including postural correction exercises, diaphragmatic breathing, spinal mobility exercises, stretching of muscles on the concave side of the curve, and general strengthening exercises for trunk, pelvic, and shoulder girdle musculature. The program was delivered three times per week for 12 weeks, with each session lasting 45 minutes.

Behavioral: Traditional Rehabilitation exercises program

Interventions

Core stabilization Exercises programBEHAVIORAL

A supervised core stabilization exercise program targeting deep and global trunk musculature including the transversus abdominis, multifidus, pelvic floor, diaphragm, rectus abdominis, erector spinae, and oblique muscles. The program was delivered three times per week for 12 weeks, with each session lasting 45 minutes. Exercises were progressively advanced from static to dynamic tasks according to participant tolerance and performance.

core stabilization exercises group
Traditional Rehabilitation exercises programBEHAVIORAL

Conventional Rehabilitation exercises commonly used in clinical practice for adolescents with idiopathic scoliosis

Traditional Rehabilitation Exercise Program

Eligibility Criteria

Age11 Years - 18 Years
Sexfemale(Gender-based eligibility)
Gender Eligibility DetailsParticipants who are biological Female
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • Female adolescents aged 11-18 years
  • Diagnosed with idiopathic scoliosis
  • Cobb's angle between 10° and 40°
  • Referred to physiotherapy

You may not qualify if:

  • Congenital, neuromuscular, or secondary scoliosis
  • Previous spine surgery or spinal correction
  • Presence of rheumatologic, renal, cardiovascular, pulmonary, or vestibular disorders
  • Inability to follow verbal instructions

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Armed Forces Hospital Southern Region

Khamis Mushait, 62462, Saudi Arabia

Location

Central Study Contacts

Hind K AlQahtani, BSc

CONTACT

+966534819676hindkhalidq@gmail.com

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER GOV
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal investigator (physiotherapist)

Study Record Dates

First Submitted

January 16, 2026

First Posted

January 23, 2026

Study Start

February 1, 2026

Primary Completion (Estimated)

November 1, 2026

Study Completion (Estimated)

December 1, 2026

Last Updated

January 27, 2026

Record last verified: 2026-01

Data Sharing

IPD Sharing
Will not share

Locations

SA(1)