- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07393724
Enhancing Tooth Reduction Skill in Fixed Prosthodontics Using Case-Based Learning Among Dental Students
January 30, 2026 updated by: Dr. Moaz Mohamed
Enhancing Tooth Reduction Skill in Fixed Prosthodontics Using Case-Based Learning Among Dental Students: A Quasi-Experimental Study
This study aimed to evaluate the effectiveness of CBL compared to traditional lecture-demonstration methods in enhancing the foundational knowledge and practical tooth reduction skills of dental students in fixed prosthodontics.
Participants were assigned to an experimental group (n=30) receiving four weekly 90-minute CBL sessions and a control group (n=30) receiving traditional lectures and clinical demonstrations
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
60
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
-
-
-
Tanta, Egypt
- Moaz EltoRKY
-
-
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
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Undergraduate preclinical dental students enrolled in the fixed prosthodontics course.
- Students who agreed to participate and provided informed consent.
Exclusion Criteria:
- Students who had previously received formal training in case-based learning (CBL) methodology.
- Students with more than 25% absence rate in regular prosthodontics classes.
- Students who had previously failed the fixed prosthodontics course.
- Individuals with physical limitations that might affect their performance in practical assessments.
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: Other
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Conventional teaching group
Participants received conventional teaching methods as part of the standard fixed prosthodontics curriculum.
|
Traditional lecture-based teaching delivered as part of the standard fixed prosthodontics curriculum.
|
|
Experimental: Case-Based Learning (CBL) group
Participants received a case-based learning (CBL) educational intervention in fixed prosthodontics.
|
A structured case-based learning approach was used to support active learning, clinical reasoning, and application of theoretical knowledge during fixed prosthodontics teaching sessions.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Theoretical knowledge examination score
Time Frame: At the end of the educational intervention (up to 4 weeks)
|
Students' theoretical knowledge in teeth preparation in fixed prsothdontics was assessed using scores obtained from a structured written theoretical examination (score range: 0-10), where higher scores indicate better theoretical knowledge.
The examination was conducted as part of the course assessment.
|
At the end of the educational intervention (up to 4 weeks)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: moaz MO osama ahmed, PHD, Faculty of Dentistry, Tanta 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 1, 2025
Primary Completion (Actual)
August 30, 2025
Study Completion (Actual)
December 30, 2025
Study Registration Dates
First Submitted
January 23, 2026
First Submitted That Met QC Criteria
January 30, 2026
First Posted (Actual)
February 6, 2026
Study Record Updates
Last Update Posted (Actual)
February 6, 2026
Last Update Submitted That Met QC Criteria
January 30, 2026
Last Verified
January 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- R-FP-7-25-3209
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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