Functionality and Clinical Correlates in TMD

NCT ID: NCT06937502

Last Updated: 2025-06-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

62 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-06-10

Study Completion Date

2025-08-10

Brief Summary

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Temporomandibular disorders (TMD) are among the most common causes of orofacial pain and refer to structural and functional impairments related to the masticatory muscles, surrounding soft tissues, and/or the temporomandibular joint (TMJ). They negatively affect individuals physically, psychologically, and socially. The structural and functional impairments observed in TMD typically manifest as pain, restricted jaw movement, joint sounds, and muscle tension. In addition to these core symptoms, secondary issues such as chewing difficulties may also occur. Pain in TMD can negatively impact many orofacial functions, especially chewing. Functional impairment in individuals with TMD may result from pain, restricted jaw mobility, muscle tension, alterations in muscle activation, mandibular asymmetry, and morphological changes in the joint. These findings highlight the importance of addressing factors associated with functional impairment in individuals with TMD.

Pain severity is strongly associated with functional limitations of the TMJ and neck disability. Particularly in cases of muscular-origin TMD, significant impairments in neck muscle function and joint mobility have been observed. This condition directly affects jaw function and leads to a decrease in quality of life. The impact of TMD on quality of life is directly related to pain severity and functional limitations. As pain severity increases, limitations in daily activities and reductions in overall quality of life also increase. Therefore, a multidisciplinary approach to TMD is essential for pain management, functional rehabilitation, and improving quality of life.

The aim of this study is to investigate the relationships between functionality and pain, range of motion, neck disability, and quality of life in individuals with TMD. Understanding these relationships will form a basis for the effective management of TMD and improving individuals' quality of life.

Detailed Description

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Conditions

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Temporomandibular Disorders (TMD) Functional Limitation Pain Severity Neck Disability Quality of Life

Study Design

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Observational Model Type

OTHER

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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Temporomandibular Disorders - Functionality Study Group

Mandibular functionality will be assessed using the Mandibular Function Impairment Questionnaire. Active temporomandibular joint (TMJ) range of motion (ROM) will be measured with a caliper. Pain will be evaluated using the Visual Analog Scale (VAS), neck disability using the Neck Disability Index (NDI), and quality of life using the World Health Organization Quality of Life Questionnaire (WHOQOL).

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Voluntary participation in the study
* Aged between 18 and 55 years
* Diagnosed with temporomandibular disorders (TMD) and exhibiting at least one of the three main symptoms (jaw pain, limited mouth opening, and/or temporomandibular joint sound)
* A Mini-Mental State Examination (MMSE) score of 24 or higher
* Pain score of 3 or above on the Visual Analog Scale (VAS)

Exclusion Criteria

* History of complex surgery, trauma, chemoradiotherapy, and/or tumors involving the head and neck region
* Ongoing use of analgesics, anti-inflammatory or psychiatric medications, and/or substance abuse
* Significant tooth loss that interferes with chewing function
* Use of dental prosthesis
* Ongoing tooth pain
* Receiving any TMD-specific treatment prior to or during the evaluation period
* History of orthodontic treatment
* Diagnosis of disc displacement without reduction
Minimum Eligible Age

18 Years

Maximum Eligible Age

55 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Istinye University

OTHER

Sponsor Role lead

Responsible Party

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Elif Kabasakal

LECTURER

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Istınye University, Istanbul,

Istanbul, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Central Contacts

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Elif Kabasakal, MSc

Role: CONTACT

05347093738

Facility Contacts

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Elif Kabasakal

Role: primary

05347093738

Other Identifiers

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ISU-2025-003

Identifier Type: -

Identifier Source: org_study_id

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