The Use of a Pediatric Trauma Checklist to Improve Clinical Performance in a Simulated Trauma Resuscitation
1 other identifier
interventional
56
1 country
1
Brief Summary
The use of a pre-arrival and pre-departure trauma checklist to optimize care has not yet been studied. The Alberta Children's Hospital (ACH) Trauma Checklist was developed by the ACH Resuscitation Council with input from the ACH Trauma Program. The purpose of this study is to determine if the introduction of the ACH Trauma Checklist as a cognitive aid, coupled with an educational session, will improve clinical performance in a simulated environment. The investigators plan to conduct a pilot, randomized control trial assessing the impact of the ACH trauma checklist on time to critical interventions on a simulated pediatric patient by multidisciplinary teams. The investigators hypothesize that teams who use a trauma checklist as a cognitive aid will have faster initiation of key clinical interventions within a simulated pediatric trauma resuscitation. Improvements in performance in a simulated environment with this tool may translate to similar results in the clinical setting.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Nov 2016
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
November 1, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2017
CompletedStudy Completion
Last participant's last visit for all outcomes
January 1, 2017
CompletedFirst Submitted
Initial submission to the registry
January 3, 2017
CompletedFirst Posted
Study publicly available on registry
July 31, 2017
CompletedJuly 31, 2017
July 1, 2017
2 months
January 3, 2017
July 28, 2017
Conditions
Keywords
Outcome Measures
Primary Outcomes (10)
Time measurement interval to initiation of endotracheal tube placement
Interval from start of scenario to endotracheal tube placement
within the 20 minute simulation scenario
Time measurement interval to initiation of induction medication
Interval from start of scenario to delivery of intubation induction medication
within the 20 minute simulation scenario
Time measurement interval to initiation of paralytic medication
Interval from start of scenario to delivery of intubation paralytic medication
within the 20 minute simulation scenario
Time measurement interval to initiation of bag mask ventilation
Interval from start of scenario to first assisted bag mask breath
within the 20 minute simulation scenario
Time measurement interval to initiation of fluid bolus administration
Interval from start of scenario to initiation of first crystalloid fluid bolus
within the 20 minute simulation scenario
Time measurement interval to initiation of blood product administration
Interval from start of scenario to initiation of first blood product administration
within the 20 minute simulation scenario
Time measurement interval to application of pelvic binder
Interval from start of scenario to application of pelvic binder
within the 20 minute simulation scenario
Time measurement interval to Glasgow Coma Score calculation
Interval from start of scenario to first verbalized and calculated Glasgow Coma Score
within the 20 minute simulation scenario
Time measurement interval to initiation of hyperosmolar therapy
Interval from start of scenario to initiation of hyperosmolar therapy, either mannitol or 3% saline
within the 20 minute simulation scenario
Time measurement interval to completion of log roll
Interval from start of scenario to completion of patient log roll
within the 20 minute simulation scenario
Secondary Outcomes (3)
Advanced Trauma Life Support Task Performance
within the 20 minute simulation scenario
Checklist completion
within the 20 minute simulation scenario
Eye movements of the trauma team leader
within the 20 minute simulation scenario
Study Arms (2)
Control Arm
NO INTERVENTIONIn the control arm, teams will not receive a copy of the checklist for use.
Checklist Arm
EXPERIMENTALIn the intervention arm, the participants will watch a 10 minute recorded educational video demonstrating the use of the trauma checklist prior to their simulation scenario. These teams will subsequently receive a copy of the checklist for use during their simulation scenario.
Interventions
The Alberta Children's Hospital Trauma Checklist was developed by the ACH Resuscitation Council Trauma Committee in response to a quality assurance review of high-acuity trauma activations. It is a cognitive aid and focuses in particular on pre-arrival preparation and a pre-departure review prior to patient transfer to diagnostic imaging or the operating room.
Eligibility Criteria
You may qualify if:
- Pediatric emergency medicine physician
- Pediatric emergency medicine physician
- Pediatric emergency registered nurse
You may not qualify if:
- Previous participation in the study
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- KidSIM Simulation Programlead
- KidSIM-ASPIREcollaborator
Study Sites (1)
KidSIM, Alberta Children's Hospital
Calgary, Alberta, T3B6A8, Canada
MeSH Terms
Conditions
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Adam Cheng, MD FRCPC
Alberta Children's Hospital, University of Calgary, KidSIM
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- NETWORK
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 3, 2017
First Posted
July 31, 2017
Study Start
November 1, 2016
Primary Completion
January 1, 2017
Study Completion
January 1, 2017
Last Updated
July 31, 2017
Record last verified: 2017-07
Data Sharing
- IPD Sharing
- Will not share