- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03258073
Does Simulation Scenario Execution Improve Acute Care Skills and Confidence Related to Maternal and Pediatric Care Emergencies? (SimForLife)
Impact of Simulation Scenario Execution on Acute Care Skills and Confidence Related to Maternal and Pediatric Care Emergencies Among Pre-service Health Professional Trainees in Uganda
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
In Uganda and many countries in Sub-Saharan Africa, health providers have minimal training and intermittent opportunity to maintain skills in managing delivery complications and acute newborn and pediatric conditions. Interventions like effective resuscitation assistance at the time of birth are lifesaving. Every 30 second delay in establishing effective resuscitation at birth increases the risk of death by 16%. The purpose of this study is to test whether medical simulation can improve acute care skills and confidence related to maternal and pediatric care emergencies.
A solid body of evidence now supports simulation-based learning as superior to didactic teaching and problem-based learning for the acquisition of critical assessment and management skills, particularly for clinical emergencies. Simulation-based training promotes skill acquisition and retention, enhances teamwork, and increases knowledge and understanding of key procedures. Simulation-based learning is now the norm in medical, nursing and paramedical training in most high income settings. There remains a critical need to operationalize simulation-based learning in resource-constrained settings
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
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Mbarara, Uganda, 256
- Mbarara University of Science and Technology
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Participants are medical and nursing students in active clinical rotation; third and fifth year medical students and third and fourth year nursing students at Mbarara University of Science and Technology.
Exclusion Criteria:
- Exclude medical and nursing students in the pre-clinical years and those in non-clinical rotations at the time of the intervention.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: OTHER
- Allocation: NA
- Interventional Model: SINGLE_GROUP
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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EXPERIMENTAL: Medical simulation using scenarion execution
Study participants will be exposed to medical simulation using scenario execution.
In this exercise, participants will be exposed to a scenario that simulates a medical emergency.
They will be required to respond.
Following their response, the participants will have a chance to share with the investigators their experiences and what they have learnt from the exposure in a debriefing session.
The investigator will then provide feedback on their performance.
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Each team of students will be exposed to simulation two times in a semester totaling to four times a year.
In a scenario execution, participants are placed in a simulated experience of a medical emergency.
Participants are required to respond and their reactions are observed by the investigators.
After the experience, participants will have a debriefing session to learn from their experience of handling this emergency.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Skills using the Scenario-execution-group test score
Time Frame: Immediately Post scenario execution
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This is a scenario specific score obtained from a multiple choice question (MCQ) test following execution of the scenario to measure.
The MCQs are standard questions developed to accompany a given scenario.
The maximum score is 100%.
A scenario-execution-group test score of less than 60% will be a fail and a score of more than or equal to 60% will be a pass.
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Immediately Post scenario execution
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Knowledge
Time Frame: Change in knowledge scores at 4 months from Baseline
|
Knowledge will be measured using multiple choice questions (MCQs) and Investigators will use the Retrospective pre-post survey (RPP survey) to assess performance confidence among participants.
In the RPP, the participant is asked to compare their performance after the intervention with that before the intervention.
This assessment removes the bias of over or underestimating how much the participant knew before the intervention.
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Change in knowledge scores at 4 months from Baseline
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Collaborators and Investigators
Collaborators
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- MUST 21/06-16b
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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