- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06583044
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
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
-
-
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Bolu, Turkey, 14030
- Bolu abant Izzet Baysal University
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-
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.
Sponsor
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
Keywords
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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