NCT06092320

Brief Summary

The goal of the randomized educational intervention study is to test whether simulation preceding didactic teaching leads to improved knowledge and performance retention compared to a didactic lecture proceeding simulation for medical students Participants will be randomized to one of two different groups with reverse orders for simulation and lectures. Researchers will compare each group to see which way is better for learning.

Trial Health

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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
40

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Sep 2023

Geographic Reach
1 country

1 active site

Status
recruiting

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

September 20, 2023

Completed
13 days until next milestone

First Submitted

Initial submission to the registry

October 3, 2023

Completed
20 days until next milestone

First Posted

Study publicly available on registry

October 23, 2023

Completed
1.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2025

Completed
Last Updated

July 5, 2024

Status Verified

July 1, 2024

Enrollment Period

1.7 years

First QC Date

October 3, 2023

Last Update Submit

July 3, 2024

Conditions

Keywords

Medical EducationSimulationPediatrics

Outcome Measures

Primary Outcomes (1)

  • Change from baseline in resuscitation performance retention score 2 months post-initial training assessed using global simulation performance score

    The scoring sheet used will be the Global Simulation performance score a one to seven scale that assess over medical expertise performance in the simulation with higher values representing increased competence.

    From initial simulation until repeat simulation 2 months later

Secondary Outcomes (3)

  • Change in knowledge assessment score at 2 months post-initial training assessed using an MCQ

    From initial knowledge test until repeat testing 2 months later

  • Learner satisfaction measured by Likert scale items after each simulation debrief

    Single time metric completed five minutes after initial simulation session

  • Time to resuscitation metrics

    The time for each metric will be measured once during the second evaluatory simulation 2 months after the initial simulation and participant enrolment.

Study Arms (2)

Simulation - Didactic Lecture Group

EXPERIMENTAL

This group will start with a Simulation and debrief followed by a didactic lecture afterwards. They will then complete a simulation 2 months later.

Other: Simulation on Pediatric Status EpilepticusOther: Didactic Lecture on Pediatric Status Epilepticus

Didactic Lecture - Simulation Group

EXPERIMENTAL

This group will start with a didactic lecture and then complete a simulation and debrief. They will then complete a simulation 2 months later.

Other: Simulation on Pediatric Status EpilepticusOther: Didactic Lecture on Pediatric Status Epilepticus

Interventions

The participants will complete a simulation session and debrief lead by a pediatric emergency medicine physician on status epilepticus.

Didactic Lecture - Simulation GroupSimulation - Didactic Lecture Group

The participants will complete a lecture on pediatric status epilepticus

Didactic Lecture - Simulation GroupSimulation - Didactic Lecture Group

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • \- Second year medical student at the University of British Columbia

You may not qualify if:

  • \- None

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

BC Children's Hospital

Vancouver, British Columbia, V6H 3N1, Canada

RECRUITING

Study Officials

  • Melissa Chan, MD

    Provincial Health Services Authority British Columbia

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Masking Details
Participants will not know the specific pediatric resuscitation simulation they will be completing. Simulation reviewers will not know which arm of the intervention the participants are in.
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principle Investigator

Study Record Dates

First Submitted

October 3, 2023

First Posted

October 23, 2023

Study Start

September 20, 2023

Primary Completion

June 1, 2025

Study Completion

June 1, 2025

Last Updated

July 5, 2024

Record last verified: 2024-07

Data Sharing

IPD Sharing
Will not share

Locations