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OpenTrials
Completed

NCT Number: NCT04677140

Hip Related Functional Limitations in Individuals With Idiopathic Scoliosis

The aim of this study is to examine the functional parameters of hip and jaw in terms of scoliosis degree and scoliosis pattern in individuals with idiopathic scoliosis.

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Key information

Age range

10 year–30 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Hacettepe University Physical Therapy and Rehabilitation Faculty

Ankara, Turkey (Türkiye)

About this study

In this study investigators will examine the hip functional parameters and jaw functional parameters separately.

In hip study hip functional parameters will be evaluated for determining the correlation between scoliosis degree/pattern and hip functions.

In jaw study jaw functional parameters will be evaluated for determining the correlation between scoliosis degree/pattern and hip functions.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

(for all hip and jaw evaluation)

  • Having been diagnosed with adolescent idiopathic scoliosis by a specialist physician with existing anterior-posterior and lateral lateral radiographs,
  • Primary curvature over 10 degrees in the coronal plane according to the Cobb method,
  • Being literate,
  • To cooperate in answering and implementing evaluation scales,
  • Children with written consent from their parents and themselves will be included.

Exclusion criteria

(for hip evaluation)

  • Having any systemic illness,
  • Spinal surgery history,
  • Presence of any acute or chronic disease other than scoliosis,
  • Inadequate quality to examine the measurement parameters of the current vertebral radiography,
  • Use of musical instruments,
  • Long-term and professional sports.

Exclusion criteria

(for jaw evaluation)

  • Having any systemic illness,
  • Spinal surgery history,
  • Presence of any acute or chronic disease other than scoliosis,
  • Aesthetics or any injection intervention in the face and neck area,
  • Spinal surgery history,
  • Orthodontic treatment,
  • Use of musical instruments,
  • Long-term and professional sports.

Treatment and study plan

Primary outcomes

  1. single leg squat test (SLS)

    Time frame: Baseline

    single leg squat test will be evaluated for each patient (min:0, max:3)

Secondary outcomes

  1. Y balance test (YBT)

    Time frame: Baseline

    Y balance test will be evaluated (cm)

Other outcomes

  1. Hip ROM (range of motion)

    Time frame: Baseline

    Hip ROM (range of motion) will be evaluated with goniometer (degree)

Sponsors and collaborators

Lead sponsor

Hacettepe University

Other

Registry information

Important dates

Study start
2020
Primary completion
2021
Study completion
2021
First posted
Dec 21, 2020
Registry last updated
Mar 16, 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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