Testing of Cognitive Behavioral Therapy Resource of Turkish Version

March 17, 2022 updated by: Aliye Tugce Gurcan, Altinbas University

Adaptation and Testing of Cognitive Behavioral Therapy Resource of Turkish Version of ''Message to Dentist'' to Reduce Dental Anxiety in Children

This study aimed to evaluate the cognitive behavioral therapy source of Turkish version of the 'message to dentist' (MTD) with children attending two dental settings.

Study Overview

Status

Completed

Conditions

Detailed Description

Children aged 5-16 years attending a dental faculty clinic and a private dental office were invited to complete the MTD form. Children were asked to report how worried they felt, their level of pain they anticipated and the actual level of pain they experienced on a scale of 1-10 (with 1 being the best outcome).

Study Type

Interventional

Enrollment (Actual)

262

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Istanbul, Turkey, 34147
        • Altinba University Faculty of Dentistry
    • Bakirkoy
      • Istanbul, Bakirkoy, Turkey, 34147
        • Altinbas University, Faculty of Dentistry

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

5 years to 15 years (Child)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

Having dental anxiety but not having negative experiences during dental treatment in childhood or adolescence

  • Without any systemical and mental diasabilities
  • Who volunteered to participate in the study and whose parental consent was obtained.

Exclusion Criteria:

  • not have dental anxiety
  • having any systemical or mental disability
  • having negative experiences during dental treatment in childhood or adolescence
  • and who did not volunteer to participate in the study and did not have parental consent for the study were excluded.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: dental anxiety group

Children,

  • Aged 5-15 years
  • Having dental anxiety but not having negative experiences during dental treatment in childhood or adolescence
  • Without any systemical and mental diasabilities
  • Who volunteered to participate in the study and whose parental consent was obtained.
Message to Dentist form

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
clinic differences and dental anxiety
Time Frame: 6 month
according to CBT form, it will be evaluated
6 month
worry type of participants
Time Frame: 6 month
according to Cognitive Behavioral Therapy form, it will be evaluated
6 month
Gender anxiety differences
Time Frame: 6 month
according to Cognitive Behavioral Therapy form, it will be evaluated
6 month

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 4, 2021

Primary Completion (Actual)

May 4, 2021

Study Completion (Actual)

August 4, 2021

Study Registration Dates

First Submitted

February 4, 2022

First Submitted That Met QC Criteria

March 15, 2022

First Posted (Actual)

March 18, 2022

Study Record Updates

Last Update Posted (Actual)

March 31, 2022

Last Update Submitted That Met QC Criteria

March 17, 2022

Last Verified

March 1, 2022

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • AltinbasU

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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