Hip Related Functional Limitations in Individuals With Idiopathic Scoliosis

March 15, 2022 updated by: Fatih Çelik, Hacettepe University
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.

Study Overview

Status

Completed

Conditions

Detailed Description

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.

Study Type

Observational

Enrollment (Actual)

60

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Turkey
      • Ankara, Turkey
        • Hacettepe University Physical Therapy and Rehabilitation Faculty

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

6 years to 26 years (Child, Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Our study will include cases who applied to Hacettepe University, Faculty of Physical Medicine and Rehabilitation with a diagnosis of scoliosis, had anterior-posterior and lateral radiographs, accepted to participate in the study on a voluntary basis, were literate and cooperated in completing the scales. In cases under the age of 18, the evaluation will be started by obtaining additional family consent.

Description

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.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Case-Only
  • Time Perspectives: Prospective

Cohorts and Interventions

Group / Cohort
experiment group
By a specialist physician with existing anteroposterior and lateral radiographs have been diagnosed with adolescent idiopathic scoliosis

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
single leg squat test (SLS)
Time Frame: Baseline
single leg squat test will be evaluated for each patient (min:0, max:3)
Baseline

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Y balance test (YBT)
Time Frame: Baseline
Y balance test will be evaluated (cm)
Baseline

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Hip ROM (range of motion)
Time Frame: Baseline
Hip ROM (range of motion) will be evaluated with goniometer (degree)
Baseline

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Hacettepe University

Investigators

  • Study Director: Gözde Yağcı, Associate Professor

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 1, 2020

Primary Completion (Actual)

September 15, 2021

Study Completion (Actual)

November 1, 2021

Study Registration Dates

First Submitted

December 3, 2020

First Submitted That Met QC Criteria

December 18, 2020

First Posted (Actual)

December 21, 2020

Study Record Updates

Last Update Posted (Actual)

March 16, 2022

Last Update Submitted That Met QC Criteria

March 15, 2022

Last Verified

March 1, 2022

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • GO 20/694

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Undecided

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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