Viewing Study NCT06186830



Ignite Creation Date: 2024-05-06 @ 7:55 PM
Last Modification Date: 2024-10-26 @ 3:17 PM
Study NCT ID: NCT06186830
Status: RECRUITING
Last Update Posted: 2024-01-02
First Post: 2023-12-17

Brief Title: Cognitive Exercise Therapy Approach Biopsychosocial Questionnaire BETY-BQ in Patient with Temporomandibular Disorders
Sponsor: Hacettepe University
Organization: Hacettepe University

Study Overview

Official Title: Validity Reliability and Responsiveness of the Cognitive Exercise Therapy Approach Biopsychosocial Questionnaire in Individuals with Temporomandibular Disorder
Status: RECRUITING
Status Verified Date: 2023-12
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: 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

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None