- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04864756
Simulation Based Learning and Academic Performance in Medical School
Medical Simulation Teaching and Academic Performance Among Medical Students at a Medical School in Rural Uganda
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Simulation faculty development will be measured by retention and engagement in simulation sessions. The investigators will use survival analysis methods and plot Kaplan Meier curves to calculate probability of retention and determine the factors that are associated with retention as derived from participant in-depth interviews and departmental meetings. A faculty member will be considered disengaged if they do not participate in simulation session for at least 6 months post training, despite reminders and opportunities for participation. Reasons for potential disengagement will be explored qualitatively.
In the qualitative approach, the investigators will conduct in-depth key informant interviews (45 minutes to 1 hour) with administrators at the institution, namely Academic Registrar, Deans of Medical School, heads of Departments and Simulation facilitators (the post-graduate student trainers). The investigators will conduct focus group discussions (1 hour) with postgraduate simulation facilitators, the medical and nursing students before, during and after their enrollment in SBL. The interviews and focus group discussions will be audio-recorded and transcribed.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Data Santorino, MD
- Phone Number: 0774500571
- Email: sdata@must.ac.ug
Study Contact Backup
- Name: Francis Bajunirwe, MD, PhD
- Phone Number: 0772 576 396
- Email: fbaj@must.ac.ug
Study Locations
-
-
-
Mbarara, Uganda, 256
- Recruiting
- Mbarara University of Science and Technology
-
Contact:
- Data Santorino, MD
- Phone Number: 0774500571
- Email: sdata@must.ac.ug
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Medical (Medicine and Nursing) students
- Enrolled in the Faculty of medicine at Mbarara University of Science and Technology
- Currently attending clinical years
Exclusion Criteria:
- Non clinical student years in the Faculty of Medicine
- not enrolled in Medicine or Nursing programs at Mbarara University of Science and Technology
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Before/After
Grade performance before and after introduction of simulation based learning
|
Learning for medical students using simulation based techniques including scenario execution as a complement to conventional teaching methodologies
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Academic performance
Time Frame: 36 months after introduction of simulation based techniques
|
Change in CGPA scores Before and after introduction of simulation based techniques
|
36 months after introduction of simulation based techniques
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Retention of academic faculty
Time Frame: 2 years after initiation of simulation based learning
|
Percentage of faculty retained in the training program
|
2 years after initiation of simulation based learning
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 2020/MUST/SIM-II
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- ICF
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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