- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06503575
Adolescent Idiopathic Scoliosis and Body Schema
May 21, 2026 updated by: Nuray Alaca, Acibadem University
Investigation of Body Schema as Sensorimotor Representation in Adolescent Idiopathic Scoliosis and Comparison With Healthy Individuals-A Case Control Study
Adolescent idiopathic scoliosis is the most common form of scoliosis.
Although an increasing number of studies suggest that an abnormal sensory-motor integration critically contributes to the cause of adolescent idiopathic scoliosis , there is uncertainty about the level of the central nervous system explaining this dysfunction.
Therefore, the planned master's thesis study aims to compare proprioception, tactile acuity, right-left reasoning ability, motor imagery ability, including the evaluation of body schema, which is a sensorimotor representation in adolescent idiopathic scoliosis patients with healthy individuals.
In addition, the relationship of these markers with posture results, body perception and quality of life of individuals with adolescent idiopathic scoliosis will be investigated as a secondary aim.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
90
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Turkey
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Istanbul, Turkey, Turkey (Türkiye), +90
- Acibadem University
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Istanbul, Turkey, Turkey (Türkiye), +90
- Maslak Acıbadem
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Probability Sample
Study Population
Adolescent idiopathic scoliosis consulting a surgeon and adolescent healthy/untreated population consulting a surgeon
Description
Inclusion Criteria (Adolescent idiopathic scoliosis)
- Diagnosis of Adolescent idiopathic scoliosis
- Age <19 years old
- Curve severity over 10°
Exclusion Criteria (Adolescent idiopathic scoliosis)
- History of spine surgery
- Surgery or trauma
- Secondary scoliosis
- Unable to fill out the questionnaires or attend the physical examination,
- History of musculoskeletal injury in the last six months
- Known systematic and psychological illness
- Use of prescription medication
Inclusion Criteria (adolescent healthy/untreated population)
-Age < 19 years Matched for age/height/weight (+/-5 years; +/- 10 lbs; +/- 10cm) to a scoliosis participant
Exclusion Criteria (adolescent healthy/untreated population)
- History of spine surgery
- Spine deformity
- Surgery or trauma
- Primer and Secondary scoliosis
- Unable to fill out the questionnaires or attend the physical examination,
- History of musculoskeletal injury in the last six months
- Known systematic and psychological illness
- Use of prescription medication
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Healthy control
|
All assessments will be made
|
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Patient with adolescent idiopathic scoliosis
|
All assessments will be made
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The two-point discrimination test
Time Frame: Baseline
|
The two-point discrimination test is used to assess if the patient is able to identify two close points on a small area of skin, and how fine the ability to discriminate this are.
It is a measure of tactile agnosia, or the inability to recognize these two points despite intact cutaneous sensation and proprioception
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Baseline
|
|
Left/right discrimination (Lateralization)
Time Frame: Baseline
|
Right-Left Discrimination will be evaluated with Recognise™ applications (Back) developed by the "Neuro Orthopedic Institute".
|
Baseline
|
|
Kinesthetic and Visual Imagery Questionnaire
Time Frame: Baseline
|
Motor imagery ability will be assessed with the Kinesthetic and Visual Imagery Questionnaire (KVIQ).
The participant gives a score between 1 and 5 for the image he/she imagines: "1 point: no image, 5 points: as clear as the original."
This process is repeated for each task and at the end of the survey, kinesthetic imagery score, visual imagery score and total score are calculated.
|
Baseline
|
|
Lumbar proprioception test
Time Frame: Baseline
|
In both groups, thoracic and lumbar repositioning accuracy will be measured and evaluated using the dual inclinometer system.
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Baseline
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Pressure Pain Threshold
Time Frame: Baseline
|
A digital pressure algometer will be applied to the web space of the foot opposite the trigger point.
Participants are instructed to say "stop" or "pain" so the stimulus can be terminated "when the sensation first transitions from pressure to pain" (pain threshold).
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Baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
4D DIERS FORMETIC
Time Frame: baseline
|
In this study, the newly developed 4D DIERS FORMETIC movable spine and surface topography evaluation device will be used.
This device is equipped with a digital network camera that allows measurements at a maximum frequency of up to 50 frames per second.
The camera uses CMOS sensors with a resolution of 1280x1024 pixels.
Thanks to these sensors and reflective markers, measurements are reconstructed in 3D.
Thus, it allows real-time evaluation of posture parameters.
Evaluation is done without radiation and without contact.
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baseline
|
|
Body Image Disturbance Questionnaire--Scoliosis Version
Time Frame: Baseline
|
It is a seven-item instrument that measures body image disturbance.
It assesses (1) concern about body part(s) felt to be unattractive; (2) preoccupation with the concern(s); (3) experiences of emotional distress about appearance; (4) impairment in social, occupational, or other areas of functioning; (5) interference with social life, school, job, or role functioning; (6) avoidance of activities because of appearance; and (7) behavioral avoidance10,26.
Using a rating scale from 1 to 5 (with 1 = not at all concerned, and 5 = extremely concerned) to measure each of these items and a mean score for the seven items, the BIDQ allows for continuous, quantitative measurement.
Higher scores reflect more severe body image disturbance
|
Baseline
|
|
Walter Reed Visual Assessment Scale
Time Frame: Baseline
|
It is a scale that scores the severity of curvature by focusing on the person's perception of posture.
It is divided into 7 parameters including body curvature, rib prominence, lumbar prominence, head-rib-pelvis positional relationship, head-pelvis relationship, shoulder level and scapula rotation.
A high score means that the perceived deformity is high.
|
Baseline
|
|
Scoliosis Research Society 22
Time Frame: Baseline
|
It is a quality of life questionnaire which consists of 22 questions assessing 5 quality of life domains: Function, Pain, Self-Image, Mental health (5 questions), satisfaction (2 questions).
Each category is rated on 5.
The categories are summed and divided by 5 to have a total score on 5 points.
5 is the best score and 1 the worst
|
Baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 15, 2024
Primary Completion (Actual)
January 15, 2025
Study Completion (Actual)
May 15, 2025
Study Registration Dates
First Submitted
July 10, 2024
First Submitted That Met QC Criteria
July 10, 2024
First Posted (Actual)
July 16, 2024
Study Record Updates
Last Update Posted (Actual)
May 26, 2026
Last Update Submitted That Met QC Criteria
May 21, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ATADEK-2024/9/343
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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