An Investigation Of The Relationship Between Temporomandibular Disorder With Posture And Pedobarographic Analysis

July 20, 2018 updated by: gizem ergezen, Istanbul Medipol University Hospital

Temporomandibular Rahatsızlığın Postür ve Pedobarografik Ölçüm Sonuçları Ile İlişkisinin Araştırılması

The aim of the study is, to evaluate the whole body posture and plantar pressure distributions in individuals with Temporomandibular Disorder and also in people with healthy temporomandibular joints. A study group aged between 18-35 years, 30 patients, who were diagnosed with Research Diagnostic Criteria for Temporomandibular Disorders (RDC/TMD) who applied us with jaw pain and 30 healthy people at the same age range as a control group were included in the study. Both groups received global postural assessments by using PostureScreen Mobile® (PSM) program which is using four side photographs and the New York Posture Scale (NYPS). Static pedobarographic measurements were taken.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

60

Phase

  • Not Applicable

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
    • Beykoz
      • Istanbul, Beykoz, Turkey, 34810
        • İstanbul Medipol 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

18 years to 35 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • clinical diagnosis of Temporomandibular Diseases
  • clinical diagnosis of healthy temporomandibular joint

Exclusion Criteria:

  • Trauma history
  • Anatomic deformities and skeletal system fractures
  • Orthopedic or rheumatic diseases diagnosed
  • Pregnancy
  • Having TMR treatment
  • Being included in the physiotherapy program in the last 6 months

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

  • Primary Purpose: Screening
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: TMD Group
people who has TMD
Other: Postural Analysis
posture and plantar pressure analysis
Other: plantar pressure analysis
posture and plantar pressure analysis
Other: Control Group
individuals who dont have healthy temporomandibular joint
Other: Postural Analysis
posture and plantar pressure analysis
Other: plantar pressure analysis
posture and plantar pressure analysis

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
flexion and extension degree
Time Frame: 5 minutes
degree
5 minutes
translation
Time Frame: 5 minutes
cm
5 minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
plantar pressure distribution
Time Frame: 2 minutes
kPa
2 minutes

Collaborators and Investigators

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

Sponsor

Istanbul Medipol University Hospital

Investigators

  • Principal Investigator: Gizem Ergezen, Medipol University
  • Study Director: Zeliha Candan Algun, Medipol 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)

April 28, 2018

Primary Completion (Actual)

May 10, 2018

Study Completion (Actual)

May 15, 2018

Study Registration Dates

First Submitted

March 25, 2018

First Submitted That Met QC Criteria

March 30, 2018

First Posted (Actual)

April 6, 2018

Study Record Updates

Last Update Posted (Actual)

July 23, 2018

Last Update Submitted That Met QC Criteria

July 20, 2018

Last Verified

May 1, 2018

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 10840098-604.01.01-E.8466

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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