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Completed

NCT Number: NCT05242601

Investigation of Quality of Life in Adolescent Idiopathic Scoliosis

the aim of our study is to identify independent predictors of quality of life in AIS.

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Key information

Age range

10 year–18 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Kırşehir Ahi Evran University

Kırşehir, 40100, Turkey (Türkiye)

About this study

Adolescent idiopathic scoliosis (AIS) is the lateral and horizontal deformity of the columna vertebralis which occurs idiopathically in adolescence ages. The aim of this study is to identify independent predictors of quality of life in AIS

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • volunteered for the study participants were diagnosed with adolescent idiopathic scoliosis,
  • between ages 10-18
  • Cobb angle between 10-30 degrees
  • Lenke curve type 1

Exclusion criteria

  • non-idiopathic scoliosis,
  • who had exercise contraindications
  • who had previous spinal surgery
  • who had orthotic treatment for scoliosis before
  • who had exercise contraindications
  • who had another neuromuscular
  • who had cardiopulmonary and rheumateulogical problem

Treatment and study plan

Primary outcomes

  1. Investigation of Quality of Life in Adolescent Idiopathic Scoliosis

    Time frame: 4 week

    Quality of life Scoliosis Research Society-22 questionnaire

Sponsors and collaborators

Lead sponsor

Kirsehir Ahi Evran Universitesi

Other

Registry information

Important dates

Study start
2021
Primary completion
2021
Study completion
2021
First posted
Feb 16, 2022
Registry last updated
Jul 26, 2022

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.

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