- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06722833
Physiotherapy Investigation in Patient With Temporomandibular Joint Dysfunction
Investigation of Pain, Function and Audiovestibular System Features in Individuals With Temporomandibular Joint Dysfunction
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.
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Tuba Kolaylı Çerezci, PhD(c)
- Phone Number: (216)4002222
- Email: tuba.kolayli@uskudar.edu.tr
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- 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
Exclusion Criteria:
- 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
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Visual Analog Scale
Time Frame: 1 day (The evaluation will be done one-time)
|
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
Time Frame: 1 day (The evaluation will be done one-time)
|
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 Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Measurement of Temporomandibular Joint Mobility
Time Frame: 1 day (The evaluation will be done one-time)
|
Individuals will be instructed to open their mouths as wide as possible without causing pain and joint mobility will be measured and recorded using a millimetric ruler.
TMJ movements in all directions will be measured three times and the average of the measurements will be recorded and noted.
|
1 day (The evaluation will be done one-time)
|
|
Immittancemetric Evaluation
Time Frame: 1 day (The evaluation will be done one-time)
|
Before tympanometric evaluation, otoscopic examination is performed.
Tympanometry, acoustic reflex and eustachian tube function tests are performed with the Interacoustics® Titan Handheld (Denmark) device.
|
1 day (The evaluation will be done one-time)
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Filiz Eyüboğlu, PhD, Uskudar University
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- tmjstudy1
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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