NCT06722833

Brief Summary

Knowing the associated factors for people suffering from TMD may help to develop preventive, therapeutic and health strategies. The aim of this study was to present the assessments of audiovestibular symptoms in people with TMD. The main question it aims to answer is the questions are as follows: 1\. Is there a relationship between TMJ symptoms and audiovestibular assessment in people with TMD? Participants will: Participants diagnosed with TMD will be informed about the study and informed consent will be obtained. Data obtained after the TMJ and vestibular system evaluation of the participants will be analyzed.

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
70

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Dec 2024

Shorter than P25 for all trials

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 4, 2024

Completed
5 days until next milestone

First Posted

Study publicly available on registry

December 9, 2024

Completed
21 days until next milestone

Study Start

First participant enrolled

December 30, 2024

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 30, 2025

Completed
1 day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2025

Completed
Last Updated

December 9, 2024

Status Verified

December 1, 2024

Enrollment Period

4 months

First QC Date

December 4, 2024

Last Update Submit

December 6, 2024

Conditions

Keywords

temporomandibular dysfunctionpain

Outcome Measures

Primary Outcomes (2)

  • Visual Analog Scale

    Visual analog scale (VAS) will be used to assess the pain intensity of individuals related to TMJD. The individual will be asked to mark the perceived pain intensity on a 10 cm long horizontal line. The individual's pain intensity will be recorded by measuring the distance the individual marks on the line in millimeters.

    1 day (The evaluation will be done one-time)

  • Evaluation of Temporomandibular Joint Functional Status

    Mandibular Dysfunction Questionnaire (MFBA) was administered to individuals to assess the functional status of the joint and the level of functional impairment that its dysfunction may cause.

    1 day (The evaluation will be done one-time)

Secondary Outcomes (2)

  • Measurement of Temporomandibular Joint Mobility

    1 day (The evaluation will be done one-time)

  • Immittancemetric Evaluation

    1 day (The evaluation will be done one-time)

Eligibility Criteria

Age18 Years - 35 Years
Sexall
Age GroupsAdult (18-64)
Sampling MethodProbability Sample
Study Population

Young adults diagnosed with TMD

You may qualify if:

  • Volunteer to participate in the study between the ages of 18-35
  • Diagnosed with unilateral TMJ disorder at least 1 month ago according to the - Research Diagnostic Criteria of Temporomandibular Disorders (RDC/TMD) classification (Dworkin et al., 1992)
  • Having muscle tenderness and pain in the temporomandibular joint region

You may not qualify if:

  • Traumatic injuries in the same area other than TMD
  • Ear diseases that cause hearing loss
  • Dentofacial Anomalies
  • Receiving orthodontic treatment
  • Neurological diseases, vestibular or visual problems

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Temporomandibular Joint DisordersPain

Condition Hierarchy (Ancestors)

Craniomandibular DisordersMandibular DiseasesJaw DiseasesMusculoskeletal DiseasesJoint DiseasesMuscular DiseasesStomatognathic DiseasesNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Filiz Eyüboğlu, PhD

    Uskudar University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Tuba Kolaylı Çerezci, PhD(c)

CONTACT

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
CROSS SECTIONAL
Target Duration
1 Day
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
PhD

Study Record Dates

First Submitted

December 4, 2024

First Posted

December 9, 2024

Study Start

December 30, 2024

Primary Completion

April 30, 2025

Study Completion

May 1, 2025

Last Updated

December 9, 2024

Record last verified: 2024-12