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RecruitingNCT07758712Updated Oct 22, 2026

Effectiveness of a Horse Riding Simulator in Adolescents With Idiopathic Scoliosis

An interventional study of Horse Riding Simulator and Core Stabilization Exercises in Scoliosis Idiopathic Adolescent, Core Stabilization Exercise and Horseback Riding, sponsored by Bezmialem Vakif University. Recruiting at 1 site in Turkey (Türkiye). Open to participants aged 10 Years to 19 Years. Per ClinicalTrials.gov, last updated 2026-10-22.

Sponsored by Bezmialem Vakif University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started Aug 2026; still recruiting 3 months later.
Updated Oct 22, 2026Primary outcomes revisedGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
10 Years to 19 Years
Sex
All
01

Study summary

Adolescent idiopathic scoliosis (AIS) is a three-dimensional spinal deformity associated with impaired respiratory muscle strength, balance, postural control, body image, and health-related quality of life. Core stabilization exercises are widely used in the conservative management of AIS. Horse riding simulator training reproduces the multidirectional rhythmic movements of horseback riding while eliminating the potential risks associated with conventional hippotherapy and may provide additional benefits for postural control and trunk muscle activation.

The aim of this randomized controlled trial is to investigate the effects of adding horse riding simulator training to a core stabilization exercise program on respiratory muscle strength, balance, health-related quality of life, and perceived cosmetic deformity in adolescents with idiopathic scoliosis. Participants will be randomly assigned to either an experimental group receiving horse riding simulator training combined with core stabilization exercises or a control group receiving core stabilization exercises alone. Outcomes will be assessed before and after the 12-week intervention.

02

Conditions studied

  • Scoliosis Idiopathic Adolescent
  • Core Stabilization Exercise
  • Horseback Riding
  • Postural Balance

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03

In context

Scoliosis

660 studies on the registry are indexed under Scoliosis; 186 are open to participants now.

This study's planned enrollment of 30 is below the median of 45 across 386 interventional studies indexed under Scoliosis.

Browse Scoliosis studies →

Lead sponsor

Bezmialem Vakif University is the lead sponsor of 354 studies on the registry; 59 are open to participants now.

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

04

Who can participate

Ages eligible
10 Years to 19 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Diagnosis of adolescent idiopathic scoliosis
  • Age between 10 and 19 years
  • Cobb angle between 10° and 40°, measured on standing spinal radiographs
  • Willingness of the participant and, when applicable, the parent or legal guardian to participate in the study

Exclusion criteria

Exclusion Criteria:

  • Scoliosis of a non-idiopathic etiology
  • History of surgery within the previous 3 months
  • Presence of an orthopedic, neurological, or systemic condition that may prevent participation in the exercise program
  • Cognitive, communication, or behavioral disorders that may interfere with understanding instructions, answering questions, or performing the exercises
  • Participation in regular exercise on 3 or more days per week
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
30 participants (estimated)

Study arms

  • Experimental
    Horse Riding Simulator + Core Stabilization

    Participants will receive supervised 60-minute core stabilization exercises combined with 30-minute horse riding simulator training twice weekly for 12 weeks. Home-based core stabilization exercises will be performed on the remaining days of the week.

    Device: Horse Riding Simulator · Behavioral: Core Stabilization Exercises

  • Active comparator
    Core Stabilization

    Participants will receive supervised 60-minute core stabilization exercises twice weekly for 12 weeks. Home-based core stabilization exercises will be performed on the remaining days of the week.

    Behavioral: Core Stabilization Exercises

Interventions

  • DeviceHorse Riding Simulator

    Participants will receive 30-minute horse riding simulator training twice weekly for 12 weeks in addition to supervised core stabilization exercises. Each session consists of 5 minutes of warm-up at low speed, 20 minutes of training at the highest speed tolerated by the participant, and 5 minutes of cool-down at low speed.

  • BehavioralCore Stabilization Exercises

    Participants will perform supervised 60-minute core stabilization exercises twice weekly for 12 weeks. Home-based core stabilization exercises will be prescribed for the remaining days of the week.

06

What researchers measure

Primary outcomes

  1. Balance

    Balance will be assessed using the Biodex Balance System.

    Time frame: Baseline and Week 12

  2. Respiratory Muscle Strength

    Respiratory muscle strength will be assessed by measuring maximal inspiratory pressure (MIP) and maximal expiratory pressure (MEP) using a portable mouth pressure device.

    Time frame: Baseline and Week 12

  3. Cobb Angle

    The Cobb angle will be measured on standing spinal radiographs as the angle formed by the intersection of lines drawn perpendicular to the endplates of the upper and lower end vertebrae of the spinal curvature. Measurements will be recorded in degrees (°), with higher values indicating greater spinal curvature severity.

    Time frame: Baseline and Week 12

  4. Angle of Trunk Rotation

    The angle of trunk rotation will be measured using a Bunnell scoliometer during the Adam's forward bending test. Measurements will be performed by a physiotherapist at the thoracic, thoracolumbar, and lumbar regions. Values will be recorded in degrees (°), with higher values indicating greater trunk rotational asymmetry.

    Time frame: Baseline and Week 12

Secondary outcomes

  1. Health-Related Quality of Life

    Health-related quality of life will be evaluated using the Scoliosis Research Society-22 (SRS-22) questionnaire.

    Time frame: Baseline and Week 12

  2. Perceived Cosmetic Deformity

    Perceived cosmetic deformity will be assessed using the Walter Reed Visual Assessment Scale (WRVAS).

    Time frame: Baseline and Week 12

07

Study locations

1 of 1 sites recruiting
08

Updates

1 registry update since Sep 25, 2026
Primary outcomes
2 time frame changed, 2 added
What changed in the outcomes
  • AddedCobb AngleTime frame: Baseline and Week 12
  • AddedAngle of Trunk RotationTime frame: Baseline and Week 12
  • Time frameBalanceBaseline and after 12 weeks → Baseline and Week 12
  • Time frameRespiratory Muscle StrengthBaseline and after 12 weeks → Baseline and Week 12
Oct 22, 2026
Secondary outcomes
2 time frame changed
What changed in the outcomes
  • Time frameHealth-Related Quality of LifeBaseline and after 12 weeks → Baseline and Week 12
  • Time framePerceived Cosmetic DeformityBaseline and after 12 weeks → Baseline and Week 12
Oct 22, 2026
Show all 1 update
  1. Oct 22, 2026
    Primary outcomes 2 time frame changed, 2 added
    What changed in the outcomes
    • AddedCobb AngleTime frame: Baseline and Week 12
    • AddedAngle of Trunk RotationTime frame: Baseline and Week 12
    • Time frameBalanceBaseline and after 12 weeks → Baseline and Week 12
    • Time frameRespiratory Muscle StrengthBaseline and after 12 weeks → Baseline and Week 12
    Secondary outcomes 2 time frame changed
    What changed in the outcomes
    • Time frameHealth-Related Quality of LifeBaseline and after 12 weeks → Baseline and Week 12
    • Time framePerceived Cosmetic DeformityBaseline and after 12 weeks → Baseline and Week 12
    + 1 other change: verification date

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

09

Registry details

Key details

Study ID
NCT07758712
Responsible party
Sponsor
First posted
Aug 11, 2026
Start date
Aug 5, 2026
Primary completion
Jan 10, 2027 (estimated)
Completion
Jan 10, 2027 (estimated)
Last update
Oct 22, 2026

Study contacts

Sefa Yıldırım
Contact
syildirim@bezmialem.edu.tr
+905385984870

Oversight

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

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