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CompletedNCT07680374Updated Jul 2, 2026

Dance-Based Exercise in Adolescent Idiopathic Scoliosis

An interventional study of Dance-Based Exercise Program and Conventional Scoliosis Exercise Program in Scoliosis Idiopathic Adolescent, sponsored by Atlas University. Completed at 1 site in Turkey (Türkiye). Open to participants aged 10 Years to 18 Years. Per ClinicalTrials.gov, last updated 2026-07-02.

Sponsored by Atlas University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 6 months after the study started (first participant enrolled Nov 2025, registered Jun 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
24
Allocation
Randomized
Ages
10 Years to 18 Years
Sex
All
01

Study summary

This randomized controlled trial aims to investigate the effects of dance-based exercises on physical fitness, body image, and quality of life in adolescents with idiopathic scoliosis (AIS). Twenty-four participants aged 10-18 years with a Cobb angle between 10° and 30° will be randomly assigned to either a dance-based exercise group or a control group. Both groups will perform conventional scoliosis exercises, while the intervention group will additionally receive dance-based exercise sessions for six weeks. Outcome measures will include body image, scoliosis-related quality of life, physical fitness, flexibility, trunk rotation, and enjoyment of physical activity.

Read the detailed description

Adolescent idiopathic scoliosis (AIS) is a three-dimensional spinal deformity associated with physical and psychosocial impairments. Although conventional exercise programs are beneficial, maintaining long-term adherence may be challenging in adolescents. Dance-based exercise programs offer a potentially enjoyable and motivating alternative.

This prospective randomized controlled study will include 24 adolescents with AIS aged 10-18 years. Participants will be randomly allocated into an intervention group and a control group (12 participants per group). Both groups will perform conventional scoliosis exercises, while the intervention group will additionally participate in dance-based exercise sessions for six weeks.

Assessments will be conducted at baseline and after six weeks. Primary outcomes will include body image and health-related quality of life. Secondary outcomes will include physical fitness, flexibility, trunk rotation, and enjoyment of physical activity.

02

Conditions studied

  • Scoliosis Idiopathic Adolescent

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Keywords

  • scoliosis
  • dance therapy
  • physical fitness
  • quality of life
03

In context

Scoliosis

593 studies on the registry are indexed under Scoliosis; 138 are open to participants now.

This study's enrollment of 24 is below the median of 44 across 344 interventional studies indexed under Scoliosis.

Browse Scoliosis studies →

Lead sponsor

Atlas University is the lead sponsor of 91 studies on the registry; 25 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
10 Years to 18 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Age between 10 and 18 years
  • Diagnosis of adolescent idiopathic scoliosis
  • Cobb angle between 10° and 30°
  • No previous dance training
  • Not participating regularly in another exercise program

Exclusion criteria

Exclusion Criteria:

  • Previous scoliosis surgery
  • Neuromuscular or congenital scoliosis
  • Neurological, orthopedic, psychiatric, cardiovascular, or pulmonary disorders -preventing exercise participation
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
24 participants (actual)

Study arms

  • Experimental
    Dance-Based Exercise Group

    Participants will perform conventional scoliosis exercises and additional dance-based exercises for six weeks.

    Other: Dance-Based Exercise Program · Other: Conventional Scoliosis Exercise Program

  • Active comparator
    Conventional Scoliosis Exercise Program

    Participants will perform conventional scoliosis exercises during the 6-week study period.

    Other: Conventional Scoliosis Exercise Program

Interventions

  • OtherDance-Based Exercise Program

    Participants will receive dance-based exercise sessions for 6 weeks (one face-to-face and one online session per week) in addition to conventional scoliosis exercises.

  • OtherConventional Scoliosis Exercise Program

    Participants will perform only conventional scoliosis exercises for six weeks.

06

What researchers measure

Primary outcomes

  1. Flexibility-Forward Bending Test

    Spinal flexibility will be assessed using the Forward Bending Test. Participants will bend forward from a standing position with the knees fully extended and attempt to reach toward the floor. The distance between the tip of the middle finger and the floor will be measured in centimeters. Lower values indicate greater trunk and posterior chain flexibility.

    Time frame: Baseline and 6 weeks

  2. Flexibility-Lateral Flexion Test

    Trunk lateral flexibility will be assessed using the Lateral Flexion Test. Participants will perform maximal lateral trunk flexion to each side while standing with the knees extended. The distance reached by the tip of the middle finger along the lateral aspect of the thigh will be measured in centimeters. Higher values indicate greater lateral trunk flexibility.

    Time frame: Baseline and 6 Weeks

  3. Core Muscle Endurance-Trunk Flexion Test

    The endurance of the trunk flexor muscles will be assessed using the Trunk Flexion Test. Participants will maintain the standardized trunk flexion position for as long as possible. Performance will be recorded as endurance time in seconds. Higher values indicate greater trunk flexor muscle endurance.

    Time frame: Baseline and 6 weeks

  4. Core Muscle Endurance-Lateral Bridge Test

    Lateral core muscle endurance will be assessed using the Lateral Bridge Test. Participants will maintain the side bridge position for as long as possible. Endurance time will be recorded in seconds, with higher values indicating better lateral trunk muscle endurance.

    Time frame: Baseline and 6 Weeks

  5. Core Muscle Endurance - Prone Bridge Test

    Global core muscle endurance will be assessed using the Prone Bridge Test. Participants will maintain the prone bridge (plank) position for as long as possible. Performance will be recorded as endurance time in seconds. Higher values indicate greater global core muscle endurance.

    Time frame: Baseline and 6 Weeks

  6. Core Muscle Endurance- Modified Biering-Sorensen Test

    The endurance of the trunk extensor muscles will be assessed using the Modified Biering-Sørensen Test. Participants will maintain the standardized horizontal trunk position for as long as possible. Performance will be recorded as endurance time in seconds. Higher values indicate greater trunk extensor muscle endurance.

    Time frame: Baseline and 6 Weeks

  7. Functional Exercise Capacity

    6 Minute Walk Test

    Time frame: Baseline and 6 Weeks

  8. Dynamic Balance

    Y Balance

    Time frame: Baseline and 6 Weeks

  9. Trunk Rotation

    Thoracic and Lumbar Rotation Measurements

    Time frame: Baseline and 6 Weeks

  10. Body Image-Walter Reed Visual Assessment Scale

    Perceived trunk deformity will be assessed using the Walter Reed Visual Assessment Scale (WRVAS). The WRVAS is a patient-reported outcome measure consisting of seven items evaluating the perceived severity of spinal deformity through standardized illustrations. Each item is scored on a 5-point scale, yielding a total score ranging from 7 to 35. Higher scores indicate greater perceived spinal deformity.

    Time frame: Baseline and 6 Weeks

Secondary outcomes

  1. Health-Related Quality of Life-Scoliosis Research Society-22 Questionnaire

    Health-related quality of life will be assessed using the Scoliosis Research Society-22 Questionnaire (SRS-22). The questionnaire consists of 22 items evaluating five domains: function/activity, pain, self-image, mental health, and satisfaction with management. Each item is scored on a 5-point Likert scale. The total (or mean) score will be calculated, with higher scores indicating better health-related quality of life.

    Time frame: Baseline and 6 Weeks

  2. Enjoyment of Physical Activity

    Physical Activity Enjoyment Scale

    Time frame: Baseline and 6 Weeks

07

Study locations

1 site
  • Istanbul Atlas University
    Istanbul, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 2, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07680374
Lead sponsor
Atlas University
Responsible party
Meltem Kaya (Assoc. Prof., Atlas University) — Principal investigator
First posted
Jul 2, 2026
Start date
Nov 24, 2025
Primary completion
May 31, 2026
Completion
Jun 15, 2026
Last update
Jul 2, 2026

Study contacts

Meltem Kaya, Assoc. Prof.
principal investigator · Atlas University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jun 2026. You cannot join it, but the record below documents what was studied.

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