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Effect of Core Stabilization Exercises Versus Traditional Rehabilitation in Adolescent With Idiopathic Scoliosis

Efficacy of Two Different Exercises Approach: Core Stabilization Exercises Versus Traditional Rehabilitation on Adolescent Idiopathic Scoliosis-A Single Blind Randomized Control Trial

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07363226
Acronym
AIS
Enrollment
60
Registered
2026-01-23
Start date
2026-02-01
Completion date
2026-12-01
Last updated
2026-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adolescence Idiopathic Scoliosis, Adolescents, Core Stabilization Exercise, Traditional Rehabilitation

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.

Interventions

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.

BEHAVIORALTraditional Rehabilitation exercises program

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

Sponsors

Armed Forces Hospitals, Southern Region, Saudi Arabia
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
11 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

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

Exclusion criteria

* 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

Design outcomes

Primary

MeasureTime frameDescription
Change in Cobb's AngleBaseline and 12 weeksCobb's angle measured using the DIERS Formetric 4D spinal analysis system in static mode

Secondary

MeasureTime frameDescription
1. Maximum Axial Vertebral Rotation (Max AVR)Baseline and 12 weeksMeasured using DIERS Formetric 4D
Pelvic ObliquityBaseline and 12 weeksMeasured using DIERS Formetric 4D
Quality of Life (QoL)Baseline and 12 weeksThe SRS-22 questionnaire consists of 22 items scored from 1 to 5, with total scores ranging from 1 (worst outcome) to 5 (best outcome). Higher scores indicate better quality of life.

Countries

Saudi Arabia

Contacts

CONTACTHind K AlQahtani, BSc
hindkhalidq@gmail.com+966534819676

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026