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

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-64
SponsorHacettepe University

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Having received a diagnosis of temporomandibular disorder

Disqualifiers

Experiencing difficulty in cooperating to fill out the questionnaires

Being unwilling to participate in the study

Trial population

Patients with temporomandibular disorder

Trial design

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

  • Validity and reliability analyses

    Other intervention

    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.

Treatment groups

150 Participants
are divided into 1 treatment group
Group A: Patients with temporomandibular disorder1 intervention

Trial outcomes

Primary outcomes

1

Validity of BETY-BQ in measuring depression

Patient Health Questionnaire-9. Minimum and maximum values are 0 and 3 points, respectively. Higher scores mean a worse outcome.

Time frame
Baseline
2

Validity of BETY-BQ in measuring physical symptoms

Patient Health Questionnaire-15. Minimum and maximum values are 0 and 2 points, respectively. Higher scores mean a worse outcome.

Time frame
Baseline
3

Validity of BETY-BQ in measuring anxiety

Generalized Anxiety Disorder-7. Minimum and maximum values are 0 and 3 points, respectively. Higher scores mean a worse outcome.

Time frame
Baseline
4

Validity of BETY-BQ in measuring quality of life

Short Form-36. It is a 36-item valid and reliable evaluation with eight areas covering physical functioning, role limitations brought on by physical issues, bodily pain, general health perceptions, vitality, social functioning, role limitations brought on by emotional issues, and perceived mental health. The SF-36 also contains a single question called "health transition" that measures how respondents feel their over health status has changed over the course of a year.

Time frame
Baseline

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Hacettepe University

Lead sponsor

Karabuk University

Sponsor institution

Karabuk University

Collaborator