Skip to main content
OpenTrials
Completed

NCT Number: NCT06503575

Adolescent Idiopathic Scoliosis and Body Schema

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.

Completed

Looking for future studies?

Notify Me

Key information

Age range

11 year–19 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Acibadem University, Istanbul, Turkey, Turkey (Türkiye)

Loading trial locations.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Assesment

Other

All assessments will be made

Primary outcomes

  1. 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

  2. Left/right discrimination (Lateralization)

    Time frame: Baseline

    Right-Left Discrimination will be evaluated with Recognise™ applications (Back) developed by the "Neuro Orthopedic Institute".

  3. 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.

  4. Lumbar proprioception test

    Time frame: Baseline

    In both groups, thoracic and lumbar repositioning accuracy will be measured and evaluated using the dual inclinometer system.

  5. 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).

Secondary outcomes

  1. 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.

  2. 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

  3. 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.

  4. 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

Sponsors and collaborators

Lead sponsor

Acibadem University

Other

Registry information

Official study title

Investigation of Body Schema as Sensorimotor Representation in Adolescent Idiopathic Scoliosis and Comparison With Healthy Individuals-A Case Control Study

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Jul 16, 2024
Registry last updated
May 26, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.