- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06753266
Optimizing OR Simulation in MEDI 045: Bias Reduction and Strategic Improvements (OPTIMIST) (OPTIMIST)
OPTIMIST Optimizing OR Simulation in MEDI 045 Anesthesia Program: Trends, Bias Reduction, and Strategic Improvements and Shaping Future Practices OPTIMIST
Study Overview
Status
Detailed Description
The effectiveness of simulation training is crucial in medical education, particularly for skills retention and perceived effectiveness. This section evaluates the overall effectiveness of SimMan3G sessions in enhancing clinical skills among participants.
Objectives
- To analyze the correlation between the number of SimMan3G sessions and skill retention.
- To assess the perceived effectiveness of simulation training.
- To provide actionable recommendations for improving simulation training effectiveness.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Riyadh, Saudi Arabia, 11461
- King Saud University Medical City (KSUMC), College of Medicine
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Riyadh, Saudi Arabia, 11461-7805-41
- King Saud University MedicalCity
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Riyadh, Saudi Arabia, 11461
- King Saud University , College of Medicine, Anesthesia Department
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Riydh
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Riyadh, Riydh, Saudi Arabia, 11461-7805-41
- King Saud University MedicalCity
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
The study population consists of medical trainees enrolled in the MEDI 045 anesthesia program at King Saud Medical City.
Participants will include individuals with varying levels of clinical experience who are eligible for simulation-based training.
Participants will be randomly selected from a list of eligible trainees in the MEDI 045 program.
Description
Inclusion Criteria:
- Participants enrolled in the MEDI 045 anesthesia program at King Saud Medical City.
- Medical students or trainees with prior exposure to basic clinical simulation.
- Aged 18 years or older.
- Willingness to participate in simulation-based training sessions.
- Ability to provide informed consent.
Exclusion Criteria:
- Participants with prior advanced simulation training in anesthesia.
- Individuals with documented cognitive impairments or learning disabilities that may interfere with the study tasks.
- Refuse to participate in post-simulation assessments or follow-ups.
- Lack of fluency in the language of instruction used in the simulation.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Cognitive Bias in Clinical Decision-Making
Time Frame: Immediately after simulation training (within 1 day) Over 6 months post-training
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Evaluate the change in cognitive bias during simulated clinical scenarios using the Cognitive Bias Assessment Tool (CBAT). This tool assesses the presence of cognitive biases (e.g., confirmation bias, anchoring bias) in decision-making. The unit of measure will be the percentage of bias-free decisions or correct decisions made by participants, based on the CBAT scoring system. The assessment will occur immediately after simulation training (within 1 day) and again 6 months post-training to measure both immediate and long-term changes in cognitive bias. |
Immediately after simulation training (within 1 day) Over 6 months post-training
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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
- KSU-ORSim-2024
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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