Actively Recruiting
Validity, Reliability and Responsiveness of the Cognitive Exercise Therapy Approach Biopsychosocial Questionnaire in Individuals with Temporomandibular Disorder
Led by Hacettepe University · Updated on 2025-03-13
150
Participants Needed
2
Research Sites
54 weeks
Total Duration
On this page
Sponsors
H
Hacettepe University
Lead Sponsor
K
Karabuk University
Collaborating Sponsor
AI-Summary
What this Trial Is About
This research aims to evaluate the Cognitive Exercise Therapy Approach Biopsychosocial Questionnaire (BETY-BQ) in adults diagnosed with temporomandibular disorder, a condition affecting the jaw joint and muscles. The study investigates how well BETY-BQ measures depression, physical symptoms, anxiety, quality of life, disability, and function, comparing it with other established questionnaires. Researchers will also assess the stability and internal consistency of BETY-BQ. Participants will complete several questionnaires, including the BETY-BQ, 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. For reliability, a group of 30 participants will retake the BETY-BQ after two weeks. To evaluate responsiveness, the same 30 participants will complete the questionnaire again after three months. During the study, participants will be asked to fill out these questionnaires at specified intervals, allowing researchers to analyze test-retest stability and consistency over time. The main outcomes focus on the validity of BETY-BQ in measuring various mental health and functional aspects at baseline, as well as its reliability from baseline to the second week. The study is expected to run until August 2025, involving adults aged 18 to 64 years diagnosed with temporomandibular disorder.
CONDITIONS
Brief Title
Cognitive Exercise Therapy Approach Biopsychosocial Questionnaire (BETY-BQ) in Patient with Temporomandibular Disorders
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 18 to 64 years
- Having received a diagnosis of temporomandibular disorder
You will not qualify if you...
- Difficulty cooperating to fill out the questionnaires
- Unwillingness to participate in the study
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Baseline
Participants complete several questionnaires assessing depression, physical symptoms, anxiety, quality of life, disability, and function related to temporomandibular disorder.
1 visit (in-person)
Duration - 2 weeks
Questionnaires are repeated after 2 weeks to assess test-retest reliability in a subset of participants.
1 follow-up visit (in-person)
Duration - 3 months
Questionnaires are reapplied after 3 months to determine responsiveness to changes over time.
1 follow-up visit (in-person)
Trial Site Locations
Total: 2 locations
1
Karabük University
Karabük, Karabük Province, Turkey (Türkiye), 78050
Actively Recruiting
2
Hacettepe University
Ankara, Turkey (Türkiye), 06100
Actively Recruiting
Research Team
H
Harun Gençosmanoğlu, PT, MSc
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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