NCT07634003

Brief Summary

This study aims to investigate the effects of a core stabilization-based rehabilitation program following adolescent idiopathic scoliosis (AIS) surgery on radiological parameters, pain, upper extremity function, range of motion, and scapular assessment. Participants diagnosed with AIS and treated with posterior spinal fusion surgery will undergo a rehabilitation program based on core stabilization exercises. Outcome measures will include Cobb angle, vertebral rotation, Visual Analog Scale (VAS), QuickDASH, Trunk Appearance Perception Scale (TAPS), SRS-22, cervical and shoulder range of motion, and scapular assessment tests. Assessments will be conducted before and after the rehabilitation program.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
20

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started May 2025

Geographic Reach
1 country

1 active site

Status
completed

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 Start

First participant enrolled

May 28, 2025

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 30, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 30, 2026

Completed
26 days until next milestone

First Submitted

Initial submission to the registry

May 26, 2026

Completed
13 days until next milestone

First Posted

Study publicly available on registry

June 8, 2026

Completed
Last Updated

June 8, 2026

Status Verified

June 1, 2026

Enrollment Period

11 months

First QC Date

May 26, 2026

Last Update Submit

June 3, 2026

Conditions

Keywords

Adolescent Idiopathic ScoliosisRehabilitationScapulaCore StabilizationPosture

Outcome Measures

Primary Outcomes (1)

  • Scapular Assessment

    Scapular control and asymmetry were evaluated using the Lateral Scapular Slide Test (LSST), Scapular Assistance Test (SAT), and wall push-up test. LSST measures scapular asymmetry by assessing the distance between the scapula and spinal landmarks at different arm positions. Greater side-to-side differences indicate increased scapular asymmetry. SAT evaluates improvement in symptoms and scapular motion during assisted scapular upward rotation. The wall push-up test was used to assess scapular winging and scapular stability.

    10 weeks

Secondary Outcomes (1)

  • Visual Analog Scale (VAS)

    10 weeks

Other Outcomes (5)

  • QuickDASH Score

    10 weeks

  • TAPS Score

    10 weeks

  • SRS-22 Quality of Life Score

    10 weeks

  • +2 more other outcomes

Study Arms (1)

Core Stabilization Rehabilitation Group

EXPERIMENTAL

Participants received a core stabilization-based rehabilitation program after adolescent idiopathic scoliosis surgery. The program included core stabilization, postural control, and scapular stabilization exercises

Behavioral: Core Stabilization-Based Rehabilitation Program

Interventions

Participants received a core stabilization-based rehabilitation program following adolescent idiopathic scoliosis surgery. The rehabilitation program included core stabilization exercises, postural control training, scapular stabilization exercises, and functional exercise approaches.

Core Stabilization Rehabilitation Group

Eligibility Criteria

Age10 Years - 18 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • Individuals diagnosed with adolescent idiopathic scoliosis (AIS)
  • Individuals who underwent posterior spinal fusion surgery
  • Age between 10 and 18 years
  • Individuals participating in a core stabilization-based rehabilitation program
  • Individuals who agreed to participate voluntarily

You may not qualify if:

  • Presence of neurological, rheumatological, or other orthopedic disorders affecting posture or upper extremity function
  • History of additional spinal surgery
  • Cognitive impairment preventing participation in evaluations
  • Incomplete assessment data
  • Noncompliance with the rehabilitation program

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Hasan Kalyoncu University

Gaziantep, Turkey (Türkiye)

Location

Study Officials

  • Yavuz Yakut, Prof. Dr.

    Hasan Kalyoncu University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Masking Details
This is a single-group intervention study conducted without blinding.
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Model Details: Single-group interventional study evaluating the effects of a core stabilization-based rehabilitation program after adolescent idiopathic scoliosis surgery.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
physiotherapist

Study Record Dates

First Submitted

May 26, 2026

First Posted

June 8, 2026

Study Start

May 28, 2025

Primary Completion

April 30, 2026

Study Completion

April 30, 2026

Last Updated

June 8, 2026

Record last verified: 2026-06

Data Sharing

IPD Sharing
Will not share

Locations