Factors Affecting Medical Student Learning in Simulation Scenarios
1 other identifier
interventional
76
1 country
1
Brief Summary
Simulation is used to teach undergraduate and postgraduate healthcare professionals, however it is not known how best to use this resource. Using qualitative methods, this study aims to investigate how medical students learn during simulation scenarios and will compare students who are paired with peers with those who are solo during their scenarios. Video and audio data from simulations will be collected and analysed with anxiety and empathy questionnaire data and semi-structured interviews.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started May 2010
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 1, 2010
CompletedFirst Submitted
Initial submission to the registry
May 4, 2010
CompletedFirst Posted
Study publicly available on registry
May 5, 2010
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2010
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2010
CompletedJune 19, 2012
June 1, 2012
7 months
May 4, 2010
June 18, 2012
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Learning during simulation scenario as measured qualitatively
2 years
Study Arms (2)
Solo
EXPERIMENTALStudents will perform their simulation scenario solo and receive feedback within the group
Paired
EXPERIMENTALStudents will be paired with one of their peers for this simulation scenario
Interventions
Eligibility Criteria
You may qualify if:
- All final year medical students at the study university who are allocated to attend the anaesthesia special study module
You may not qualify if:
- Non-English speakers
- Visiting students who will be unable to complete the study
- Students who refuse to participate
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Oxford
Oxford, Oxfordshire, OX3 9HW, United Kingdom
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Imogen Davies, MB BCh
University of Oxford
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Clinical Lecturer
Study Record Dates
First Submitted
May 4, 2010
First Posted
May 5, 2010
Study Start
May 1, 2010
Primary Completion
December 1, 2010
Study Completion
December 1, 2010
Last Updated
June 19, 2012
Record last verified: 2012-06