Comparison of Reposition Sense in Scoliosis and Healthy Adolescents

Sponsor
Istanbul University-Cerrahpasa (Other)
Overall Status
Recruiting
CT.gov ID
NCT05187780
Collaborator
Biruni University (Other), Istanbul University (Other)
63
1
10
6.3

Study Details

Study Description

Brief Summary

The aim of the study is to compare the spine joint reposition sense in adolescent idiopathic scoliosis and healthy adolescents and to investigate whether there is a difference.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Considering the role of proprioception during activities of daily living and exercises, it is important for clinicians and researchers to determine the joint position senses of adolescents with scoliosis and to compare them with their healthy peers in planning appropriate treatment programs. In the light of this information, the aim of the study is to compare the spine joint reposition sense in adolescent idiopathic scoliosis and healthy adolescents and to investigate whether there is a difference. Patients who were diagnosed with Adolescent Idiopathic Scoliosis (AIS) in the Department of Orthopedics and Traumatology of Istanbul University and who were referred to the Department of Physiotherapy and Rehabilitation of the Faculty of Health Sciences of Istanbul University-Cerrahpaşa and Biruni University and their healthy peers will be included in the study.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    63 participants
    Observational Model:
    Other
    Time Perspective:
    Cross-Sectional
    Official Title:
    Comparison of Spinal Joint Reposition Sense in Idiopathic Scoliosis and Healthy Adolescents
    Actual Study Start Date :
    Jan 22, 2022
    Anticipated Primary Completion Date :
    Sep 22, 2022
    Anticipated Study Completion Date :
    Nov 22, 2022

    Arms and Interventions

    Arm Intervention/Treatment
    Group 1

    Adolescents with Idiopathic Scoliosis who have 10⁰-24⁰ Cobb angles

    Group 2

    Adolescents with Idiopathic Scoliosis who have 25⁰-40⁰ Cobb angles

    Group 3

    Healthy adolescents without scoliosis as controls

    Outcome Measures

    Primary Outcome Measures

    1. Evaluation of spine joint position reproduction [Baseline]

      Acumar™ Dual Inclinometer: The subjects will be asked to stay at the reference position for three seconds and then move to the upright position and then go back to the reference angle with their eyes closed. The absolute difference between the two positions in degrees will be noted as the reposition error value. The decrease in the reposition error value is considered as the improvement in the reposition sense.

    Secondary Outcome Measures

    1. Spinal pain assessment [Baseline]

      Visual Analogue Scale (VAS): It is used to quantify the pain intensity of patients. Rest, activity, and night pain will be assessed in the study. The condition that there is no pain is expressed as 0, and the condition that there is too much pain to be tolerated is expressed as 10.

    2. Physical activity level [Baseline]

      The subjects' physical activity will be assessed with the Physical Activity Questionnaire for Older Children. The questionnaire consists of a total of 9 items (21 activities) that questions the last 7 days with the form of a 5-point Likert-type. The high scores indicate a high physical activity level. Scoring is based on the frequency of the activities, 'never done' (1 point), '1-2 times' (2 points), '3-4 times' (3 points), '5-6 times' (4 points), ' 7 times and more' (5 points).

    3. Adam's Forward Bending Test [Baseline]

      The curve for the diagnosis of scoliosis will be analyzed in the Adam's forward bending test. The test will be performed with a scoliometer to measure the degree of rotation of the vertebrae in the horizontal plane in scoliosis. Rotation measured below 5 degrees is considered normal and does not require follow-up.

    4. Cobb angle assessment [Baseline]

      The Cobb method has an important role in determining the size of the spinal curve in frontal plane radiography, determining the size of the treatment, and measuring the effectiveness of the treatment. Cobb angle measurement is performed on standard anteroposterior spine radiography. In the measurement, the angle between a line drawn parallel to the upper vertebra joining the curve and a line drawn parallel to the bottom of the lowest vertebra of the same curve is calculated. The increase in the Cobb degree is considered as an indicator of the increase in the severity of the curvature.

    5. Flexicurve ruler [Baseline]

      The ruler, which has a plastic and reshapeable structure, is used for the noninvasive measurement of thoracic kyphosis. The tip of the Flexicurve is placed at C7 and shaped caudally to the contour of the thoracic spine. The Flexicurve is then carefully placed on paper and the outline of the shaped thoracic curve is drawn. This process is repeated three times, straightening the ruler between each measurement. The kyphosis index and Flexicurve angle are calculated using the formulas. The kyphosis index is calculated by dividing the apex of kyphosis by the length of the thoracic curve and multiplying by 100. A kyphosis index value greater than 13 is defined as hyperkyphosis.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    10 Years to 19 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Being between the ages of 10 and 19 years

    • Having a Cobb angle of 10-40 degrees measured on the anteroposterior radiograph or a healthy spine alignment (Forward Bend Test < 5⁰ (negative) and Flexicurve Kyphosis Index ≤13)

    • No previous conservative approach to scoliosis

    • Volunteer to participate in the study

    Exclusion Criteria:
    • Concomitant mental problem, rheumatological, neuromuscular, cardiovascular, pulmonary history

    • Any orthopedic disability or severe pain that would preclude evaluations

    • Musculoskeletal injury related to the spine in the last 3 months

    • Having had spine surgery

    • Presence of tumor in the spine

    • Loss of vision and/or hearing/presence of vestibular problems

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 İstanbul University Cerrahpasa Istanbul Turkey

    Sponsors and Collaborators

    • Istanbul University-Cerrahpasa
    • Biruni University
    • Istanbul University

    Investigators

    • Principal Investigator: Ayşe Zengin Aplözgen, PhD, Istanbul University-Cerrahpasa

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Ayse Zengin Alpozgen, Asst. Prof., Istanbul University-Cerrahpasa
    ClinicalTrials.gov Identifier:
    NCT05187780
    Other Study ID Numbers:
    • 2020/01
    First Posted:
    Jan 12, 2022
    Last Update Posted:
    Aug 4, 2022
    Last Verified:
    Aug 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Ayse Zengin Alpozgen, Asst. Prof., Istanbul University-Cerrahpasa
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 4, 2022