- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06773234
Evaluation of the Dental Educational Environment Using the DREEM Tool
January 16, 2025 updated by: Shereen Shaaban, Beni-Suef University
Evaluation of the Dental Educational Environment in Upper Egypt Using the DREEM Tool: a Cross-Sectional Study
This Cross-Sectional Study aims to evaluate the dental educational environment in Upper Egypt using the Dundee Ready Education Environment Measure (DREEM) Questionnaire.
Study Overview
Detailed Description
This Cross-Sectional Study aims to evaluate the dental educational environment in Upper Egypt using the Dundee Ready Education Environment Measure (DREEM) Questionnaire.
The questionnaire will be sent to students in Faculty of Dentistry, Beni-Suef University to assess their perception of the educational environment.
Study Type
Observational
Enrollment (Estimated)
215
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Shereen Mustafa
- Phone Number: 082 2247883
- Email: shereen.shaaban@dent.bsu.edu.eg
Study Locations
-
-
-
Banī Suwayf, Egypt
- Recruiting
- Faculty of Dentistry, Beni-Suef University.
-
Contact:
- Phone Number: 0822247883
- Email: shereen.shaaban@dent.bsu.edu.eg
-
-
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Probability Sample
Study Population
students registered in the Faculty of Dentistry, Beni-Suef University
Description
Inclusion Criteria:
- Students registered in the Faculty of Dentistry, Beni-Suef University
Exclusion Criteria:
- Students registered in any dental school other than the Faculty of Dentistry, Beni-Suef University.
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 |
|---|---|
|
students from Faculty of Dentistry, Beni-Suef University
students from different educational levels in the Faculty of Dentistry, Beni-Suef University
|
DREEM Tool
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Evaluation of dental students' perception of the educational environment.
Time Frame: 3 months
|
Outcome Measuring Unit is 5 Likert scale scores as follows Strongly agree 4, Agree 3, Unsure 2, Disagree 1, and Strongly disagree 0
|
3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Shereen Mustafa, Lecturer of Pediatric Dentistry and Dental Public Health Faculty of Dentistry, Beni-Suef 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)
December 26, 2024
Primary Completion (Estimated)
March 1, 2025
Study Completion (Estimated)
March 1, 2025
Study Registration Dates
First Submitted
December 31, 2024
First Submitted That Met QC Criteria
January 8, 2025
First Posted (Actual)
March 25, 2025
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
January 16, 2025
Last Verified
January 1, 2025
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- # REC-FDBSU/05122024-02/MS
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
product manufactured in and exported from the U.S.
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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