Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04677140
Other study ID # GO 20/694
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 1, 2020
Est. completion date November 1, 2021

Study information

Verified date March 2022
Source Hacettepe University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date November 1, 2021
Est. primary completion date September 15, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 10 Years to 30 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Locations

Country Name City State
Turkey Hacettepe University Physical Therapy and Rehabilitation Faculty Ankara

Sponsors (1)

Lead Sponsor Collaborator
Hacettepe University

Country where clinical trial is conducted

Turkey, 

References & Publications (1)

Choudhry MN, Ahmad Z, Verma R. Adolescent Idiopathic Scoliosis. Open Orthop J. 2016 May 30;10:143-54. doi: 10.2174/1874325001610010143. eCollection 2016. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Other Hip ROM (range of motion) Hip ROM (range of motion) will be evaluated with goniometer (degree) Baseline
Primary single leg squat test (SLS) single leg squat test will be evaluated for each patient (min:0, max:3) Baseline
Secondary Y balance test (YBT) Y balance test will be evaluated (cm) Baseline
See also
  Status Clinical Trial Phase
Recruiting NCT04914507 - A Prospective Analysis of Long-Term Clinical Outcomes and 3D Spine Growth in Anterior Vertebral Body Tethering N/A
Not yet recruiting NCT05830825 - PMCF (Post-Market Clinical Follow-up) Study on The Tether™ in UK (United Kingdom)
Terminated NCT03676712 - The Effect of Flexible Thoracolumbar Brace on Idiopathic Scoliosis, Prospective, Randomized, Open-label Trial N/A
Terminated NCT04538092 - Complex Spine Enhanced Recovery After Surgery (ERAS) N/A
Completed NCT04669327 - Hip and Knee Moments Normal and With Scoliosis
Completed NCT05033171 - Rod Shape Changing After Scoliosis Correction Surgery N/A
Recruiting NCT04505579 - The Tether™ - Vertebral Body Tethering System Post Approval Study
Recruiting NCT04047225 - POSTOPERATIVE OPIOID-SPARING EFFECT OF INTRAOPERATIVE PAIN MONITORING USING THE ANALGESIA NOCICEPTIVE INDEX (ANI) DURING IDIOPATHIC SCOLIOSIS CORRECTION IN CHILDREN. N/A
Recruiting NCT06086431 - Dexamethasone vs. Dexmedetomidine for ESPB in Pain Management After Pediatric Idiopathic Scoliosis Surgery Phase 4
Not yet recruiting NCT05039255 - Acute Effects of Self-correcting Movement on the Balance and Spine of Patients With Scoliosis.
Completed NCT03820895 - Vitamin D Levels in Adolescent Idiopathic Scoliosis
Recruiting NCT05045014 - Evaluation of Vestibular Dysfunction or Visuospatial Perception in Individuals With Idiopathic Scoliosis
Recruiting NCT05011734 - Rapid Postoperative Recovery Pathway in Adolescent Idiopathic Scoliosis.
Active, not recruiting NCT04343170 - Effect of Ultra-short-term Treatment of Patients With Iron Deficiency or Anemia Undergoing Adolescent Scoliosis Correction N/A
Recruiting NCT06093477 - Studying Melatonin and Recovery in Teens N/A
Completed NCT06063447 - Does Adolescent Idıopathic Scoliosis Cause Pelvic Floor Dysfunction?
Recruiting NCT06417944 - The Effect of Three-dimensional Exercise (Schroth Exercise) on Diaphragm Thickness in Adolescent Idiopathic Scoliosis Patients
Recruiting NCT05938959 - Erector Spinae Plane Block for Pediatric Idiopathic Scoliosis Surgery Phase 4
Completed NCT05298371 - The Effect of Sitting and Standing Posture on Trunk Rotation in Patients With Idiopathic Scoliosis
Active, not recruiting NCT03497520 - The Effect of Asymmetric Spinal Stabilization Exercise on Scoliosis N/A