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Comparison of Reposition Sense in Scoliosis and Healthy Adolescents

I

Istanbul University - Cerrahpasa (IUC)

Status

Enrolling

Conditions

Healthy
Scoliosis; Adolescence
Proprioception

Study type

Observational

Funder types

Other

Identifiers

NCT05187780
2020/01

Details and patient eligibility

About

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.

Full 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.

Enrollment

63 estimated patients

Sex

All

Ages

10 to 19 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

63 participants in 3 patient groups

Group 1
Description:
Adolescents with Idiopathic Scoliosis who have 10⁰-24⁰ Cobb angles
Group 2
Description:
Adolescents with Idiopathic Scoliosis who have 25⁰-40⁰ Cobb angles
Group 3
Description:
Healthy adolescents without scoliosis as controls

Trial contacts and locations

1

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Central trial contact

Begüm KARA KAYA, MSc; Ayşe Zengin Aplözgen, PhD

Data sourced from clinicaltrials.gov

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