NCT03234049

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

87
On Track

Trial Health Score

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

Enrollment
56

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Nov 2016

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 1, 2016

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2017

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2017

Completed
2 days until next milestone

First Submitted

Initial submission to the registry

January 3, 2017

Completed
7 months until next milestone

First Posted

Study publicly available on registry

July 31, 2017

Completed
Last Updated

July 31, 2017

Status Verified

July 1, 2017

Enrollment Period

2 months

First QC Date

January 3, 2017

Last Update Submit

July 28, 2017

Conditions

Keywords

pediatricchecklistcognitive aid

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 INTERVENTION

In the control arm, teams will not receive a copy of the checklist for use.

Checklist Arm

EXPERIMENTAL

In 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.

Other: Checklist

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.

Checklist Arm

Eligibility Criteria

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

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

Study Sites (1)

KidSIM, Alberta Children's Hospital

Calgary, Alberta, T3B6A8, Canada

Location

MeSH Terms

Conditions

Wounds and Injuries

Interventions

Checklist

Intervention Hierarchy (Ancestors)

Data CollectionHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and Evaluation

Study Officials

  • Adam Cheng, MD FRCPC

    Alberta Children's Hospital, University of Calgary, KidSIM

    PRINCIPAL INVESTIGATOR

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

Locations