- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05411770
The Relationship Between The Stomatognathic System, Spine Posture And Pelvic Symmetry
June 6, 2022 updated by: Sanko University
Investigation of The Relationship Between The Stomatognathic System, Spine Posture and Pelvic Symmetry in Adolescence Individuals
This study was planned to examine the relationship between the stomatognathic system, spine posture and pelvis symmetry.
91 healthy adolescence were included in the study.
For stomatognathic system, temporomandibular range of motion with millimeter ruler, cervical joint range of motion and craniovertebral angle measurement with goniometer, tragus-wall distance measurement with tape measure, kyphosis and lordosis angle measurement with Baseline Bubble Inclinometer®, trunk rotation angle scoliometer for scoliosis, lower extremity length measurements for pelvis symmetry were made using a tape measure.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
91
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
-
-
Şehitkamil
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Gaziantep, Şehitkamil, Turkey, 27620
- SANKO University
-
-
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
10 years to 18 years (ADULT, CHILD)
Accepts Healthy Volunteers
N/A
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Healthy adolescent individuals aged 10-18 years were included in the study.
Description
Inclusion Criteria:
- No known neurological, rheumatological, musculoskeletal problems
- Has no visual or hearing impairment
- Ability to adapt to the parameters to be applied in the study
- Ability to perform tests to be applied
- Consists of voluntary adolescent individuals whose families gave permission to participate in the study.
Exclusion Criteria:
- Receiving joint sounds in the form of clicks or crepitations from the TMJ during mouth opening and closing or chewing
- Passion and tenderness in the TMJ on palpation
- Having a tumor Having received orthodontic treatment in the last 3 years
- Having a history of head, neck and maxillofacial surgery
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Thoracic kyphosis and lumbar lordosis angle assessment
Time Frame: 12 Weeks
|
Thoracic kyphosis and lumbar lordosis angle assessment was performed with the reliable Baseline Bubble Inclinometer®.
|
12 Weeks
|
Temporomandibular range of motion
Time Frame: 12 Weeks
|
TMJ range of motion, maximum mouth opening amount (MAAM), right and left lateral movements of the mandible (laterotrusion), anterior movement of the mandible (protrusion), and backward movement of the mandible (retrusion) were measured with a millimetric ruler, while the adolescent was seated on a chair and recorded in mm.
|
12 Weeks
|
Measuring the cervical joint range of motion
Time Frame: 12 Weeks
|
Cervical joint flexion, extension, lateral flexion and rotation ranges of motion were measured with a universal goniometer while the adolescent was sitting in a chair.
|
12 Weeks
|
Craniovertebral angle measurement
Time Frame: 12 Weeks
|
Head posture of the adolescent was evaluated by craniovertebral angle (CVA) method.
Adolescents sat on a chair with back support in an upright position and turned sideways to the worker.
The pivot point was accepted as the seventh cervical vertebra, and the angle between the head (tragus) and the horizontal plane was measured with a goniometer and recorded in degrees.
|
12 Weeks
|
Tragus-to-wall distance measurement
Time Frame: 12 Weeks
|
Tragus-to-wall distance was measured using a tape measure and recorded in cm.
|
12 Weeks
|
Scoliosis angle assessment
Time Frame: 12 Weeks
|
Scoliosis angle assessment was done with a scoliometer.
|
12 Weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Emine Betül Demirkapi, MSc, SANKO University
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)
July 30, 2020
Primary Completion (Actual)
March 30, 2021
Study Completion (Actual)
July 30, 2021
Study Registration Dates
First Submitted
May 31, 2022
First Submitted That Met QC Criteria
June 6, 2022
First Posted (Actual)
June 9, 2022
Study Record Updates
Last Update Posted (Actual)
June 9, 2022
Last Update Submitted That Met QC Criteria
June 6, 2022
Last Verified
May 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- 2020/09
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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