- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04100928
Evaluating the Well-being Among Dental Students With Warwick-Edinburg Mental Well-Being Scale
September 24, 2019 updated by: Yasemin Sezgin, Baskent University
Evaluating the Well-being Among Dental Students With Warwick-Edinburg Mental Well-Being Scale and the Relationship Between Mental Well-being and Socio-demographic Findings
The present study was conducted to measure the mental well-being amongst dental students by using Warwick-Edinburg Mental Well-being Scale (WEMWBS) and investigate factors affecting well-being among dental students.
Study Overview
Detailed Description
The survey schedule was planned to be independent of the students' assessment period and the questionnaire was administered to the students when they were attending a lecture together.
After the lecture, a researcher explained to the students the purpose of this survey and assured them of confidentiality.
Participation in this study was also voluntary, and all participants remained anonymous.
The questionnaire was given to all participants after explaining the purpose of the study.
The questionnaire included demographic details (age, gender, year of study), social background (parents' education levels, family income, first choice for admission, living accommodation) and lifestyle behaviors (smoking status, presence of regular sport activity and hobby).
In addition, Warwick-Edinburg Mental Well-Being Scale was applied to the participants of this study.
Study Type
Observational
Enrollment (Actual)
268
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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Ankara, Turkey, 06690
- Yasemin Sezgin
-
-
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
18 years to 27 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
All students in the faculty of dentistry, Baskent University
Description
Inclusion Criteria:
to be officially registered in the faculty of dentistry, Baskent University
Exclusion Criteria:
unwilling to participate
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Warwick-Edinburg Mental Well-being Scale
Time Frame: day 1
|
Individuals completing the scale are required to tick the box that best describes their experience of each statement over the past two weeks using a 5-point Likert scale (none of the time, rarely, some of the time, often, all of the time).
The Likert scale represents a score for each item from 1 to 5 respectively, giving a minimum score of 14 and maximum score of 70.
|
day 1
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: yasemin sezgin, Dr.
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)
September 9, 2019
Primary Completion (Actual)
September 20, 2019
Study Completion (Actual)
September 21, 2019
Study Registration Dates
First Submitted
September 23, 2019
First Submitted That Met QC Criteria
September 23, 2019
First Posted (Actual)
September 24, 2019
Study Record Updates
Last Update Posted (Actual)
September 25, 2019
Last Update Submitted That Met QC Criteria
September 24, 2019
Last Verified
September 1, 2019
More Information
Terms related to this study
Other Study ID Numbers
- BaskentU6
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
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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