Bruxism Awareness in Dental Students (BADS)

August 31, 2024 updated by: Tuğba ŞAHİN, Abant Izzet Baysal University

Bruxism Awareness and Self-assessment in Dental Clinical Students: A Questionnaire Study

Clinical students in the Faculty of Dentistry were diagnosed with bruxism according to the bruxism assessment consensus 2018. A total of 128 students with (64) and without (64) bruxism, were asked 33 questions about their knowledge and self-awareness about bruxism.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

This study included systemically healthy individuals aged 18 to 27. Intraoral and extraoral examinations were performed on 128 students with (64) and without bruxism (64), 4th and 5th-grade dental students at Bolu Abant İzzet Baysal University who met the inclusion criteria. The diagnosis of bruxism was based on the 2018 International Consensus and data collected through a validated 33-item questionnaire covering general information and bruxism awareness. The questionnaire included questions on bruxism's types, risk factors, symptoms, and impact on periodontal tissues, with multiple-choice responses. Statistical analyses were performed using IBM SPSS Statistics, and p<0.05 was accepted as statistical significance

Study Type

Observational

Enrollment (Actual)

128

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

      • Bolu, Turkey, 14030
        • Bolu abant Izzet Baysal University

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

  • Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

The study included 4th and 5th dental students.

Description

Inclusion Criteria:

  • Systemically healthy individuals

Exclusion Criteria:

  • Individuals with mental retardation,
  • Individuals with suicidal tendencies,
  • Individuals with dementia,
  • Individuals with psychosis

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Dentistry clinical student diagnosed with bruxism
This group includes dental clinical students diagnosed with bruxism.
It includes 33 questions measuring awareness and knowledge about bruxism.
Dentistry clinical student without bruxism diagnosis
This group includes dental clinical students diagnosed without bruxism.
It includes 33 questions measuring awareness and knowledge about bruxism.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Bruxism Awareness Survey
Time Frame: Baseline
Determines how much information the participants have about bruxism diagnosis, symptoms, risk factors, and treatment methods. It consists of yes-no questions with two options. One is an answer.
Baseline
Bruxism Knowledge Level Survey
Time Frame: Baseline
Participants are assessed to determine the extent to which they can diagnose bruxism through self-assessment. It consists of 3 to 7 multiple-choice questions. One of the answers is the correct answer, and the assessment is based on this.
Baseline

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Bruxism symptoms Survey
Time Frame: Baseline
It includes information about whether the participants experience bruxism symptoms and the impact of these symptoms. It consists of 3 to 7 multiple-choice questions. One of the answers is the correct answer, and the assessment is based on this.
Baseline
Treatment and Follow-up Survey
Time Frame: Baseline
It includes questions about whether patients with bruxism are treated, what treatment methods are used, and whether there is an improvement in symptoms after treatment. It consists of 3 to 7 multiple-choice questions. One of the answers is the correct answer, and the assessment is based on this.
Baseline

Collaborators and Investigators

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

Investigators

  • Principal Investigator: TUGBA SAHIN, Abant Izzet Baysal University

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)

June 5, 2024

Primary Completion (Actual)

June 25, 2024

Study Completion (Actual)

June 25, 2024

Study Registration Dates

First Submitted

August 26, 2024

First Submitted That Met QC Criteria

August 31, 2024

First Posted (Actual)

September 3, 2024

Study Record Updates

Last Update Posted (Actual)

September 3, 2024

Last Update Submitted That Met QC Criteria

August 31, 2024

Last Verified

August 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • AIBU-DH-TS-03

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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