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Recruiting NCT06186830

Cognitive Exercise Therapy Approach Biopsychosocial Questionnaire (BETY-BQ) in Patient with Temporomandibular Disorders

— Observational Temporomandibular Disorder Temporomandibular Joint Disorders Temporomandibular Joint Dysfunction Syndrome

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Validity and reliability analyses.
Who it may be relevant to
Registry conditions: Temporomandibular Disorder, Temporomandibular Joint Disorders, Temporomandibular Joint Dysfunction Syndrome. Basic parameters: 18 years — 64 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Validity, Reliability and Responsiveness of the Cognitive Exercise Therapy Approach Biopsychosocial Questionnaire in Individuals with Temporomandibular Disorder

Overview

The aim of this study is to investigate the validity, reliability, and responsiveness of the Cognitive Exercise Therapy Approach-Biopsychosocial Questionnaire (BETY-BQ) in individuals with temporomandibular disorder. The following are alternative hypotheses of the study: * BETY-BQ has significant convergence with the Patient Health Questionnaire-9 measuring depression. * BETY-BQ has significant convergence with the Patient Health Questionnaire-15 measuring physical symptoms. * BETY-BQ has significant convergence with the Generalized Anxiety Disorder-7 measuring anxiety. * BETY-BQ has significant convergence with the Short Form-36 measuring quality of life. * BETY-BQ has significant convergence with the Craniomandibular Pain and Disability Inventory measuring disability. * BETY-BQ has significant convergence with the Mandibular Function Impairment Questionnaire measuring function. * BETY-BQ has significant stability. * BETY-BQ has significant internal consistency.

Detailed description

Patient Health Questionnaire-9 (Depression), Patient Health Questionnaire-15 (Physical Symptoms), Generalized Anxiety Disorder-7 (Anxiety), Short Form-36 (Quality of Life), Craniomandibular Pain and Disability Inventory (Disability), and Mandibular Function Impairment Questionnaire (Function) will be administered to participants. For reliability analysis, test-retest stability evaluations will be repeated with the same questionnaire on 30 individuals with a 2-week interval. To determine responsiveness, the same questionnaire will be reapplied to the same 30 individuals at 3-month intervals.

Interventions

  • Other Validity and reliability analyses
    Validity and reliability analyses will be performed using Cognitive Exercise Therapy Approach Biopsychosocial Questionnaire, Patient Health Questionnaire-9, Patient Health Questionnaire-15, Generalized Anxiety Disorder-7, Short Form-36, Craniomandibular Pain and Disability Inventory, and Mandibular Function Impairment Questionnaire.

Primary outcome measures

  • Validity of BETY-BQ in measuring depression [Time frame: Baseline]
  • Validity of BETY-BQ in measuring physical symptoms [Time frame: Baseline]
  • Validity of BETY-BQ in measuring anxiety [Time frame: Baseline]
  • Validity of BETY-BQ in measuring quality of life [Time frame: Baseline]
  • Validity of BETY-BQ in measuring disability [Time frame: Baseline]
  • Validity of BETY-BQ in measuring function [Time frame: Baseline]
  • Test-retest stability of BETY-BQ [Time frame: From baseline to 2nd week]
  • Internal consistency of BETY-BQ [Time frame: Baseline]

Eligibility criteria

Inclusion criteria

  • Having received a diagnosis of temporomandibular disorder

Exclusion criteria

  • Experiencing difficulty in cooperating to fill out the questionnaires
  • Being unwilling to participate in the study

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Other

Study locations

Turkey (Türkiye) · 2 centers
  • Karabük University — Karabük
  • Hacettepe University — Ankara

Identifiers

NCT: NCT06186830 · 2023/1361

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗