Pediatric Readiness Intervention in Manitoba
Improving Pediatric Readiness of Emergency Departments in Manitoba, Canada: a Randomized Controlled Trial and Survey Sampling
1 other identifier
interventional
17
1 country
1
Brief Summary
The goal of this clinical trial is to improve emergency care of children in Manitoba by increasing the weighted pediatric readiness scores (WPRS) of the general EDs through the implementation of provincially derived interventional measures (PDIM). Investigators want to test the effects of PDIM on the general EDs in Manitoba. The main questions it aims to answer are:
- What is the magnitude and direction of the effect of implementing PDIM on baseline WPRS of the general EDs, if any?
- Which implementation strategies effectively support the full incorporation of PDIM to increase the WPRS of general EDs across Manitoba? The participating general EDs will be asked to
- Gather individuals providing emergency care in their centers for training and education around PDIM.
- Select a lead person who will act as the general ED Champion.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Oct 2022
Typical duration 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
October 2, 2022
CompletedFirst Submitted
Initial submission to the registry
October 11, 2023
CompletedFirst Posted
Study publicly available on registry
February 14, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 31, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
May 31, 2025
CompletedJune 13, 2025
June 1, 2025
2.7 years
October 11, 2023
June 11, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Weighted Pediatric Readiness Scores
To be measured using the Manitoba Pediatric Readiness Initiative for Emergency department Survey
9 months
Study Arms (2)
PDIM component 1, 2, and 3
EXPERIMENTALIntervention component 2 to be tested. Pediatric resources toolkits availability via Translating Emergency Knowledge for Kids network (TREKK). Investigators will provide resource toolkits to support clinical care in pediatric sepsis, seizure, diabetes ketoacidosis, dehydration, hypovolemic shock, and respiratory conditions. Intervention component 3 to be tested: Ongoing interactions, and intensive training and education sessions. Investigators will hold training and education sessions at the sites. These will include (a) One on-site training (for 4-4.5 hours) with simulation sessions.
PDIM component 1
ACTIVE COMPARATORCustomized report to the general EDs and discussion with the general EDs on the gaps identified. Investigators will discuss customized baseline WPRS with each general ED, including implications of the gaps identified relative to their local context and the general ED priorities (1.5hrs/session x 2).
Interventions
Pediatric resource toolkits availability via TREKK for Kids Ongoing interactions, and intensive training and education sessions
Eligibility Criteria
You may qualify if:
- General ED located in Manitoba
- Offering emergency care to children aged 0-18 years during the study period
- Participated in the baseline evaluation of WPRS of the general EDs in Manitoba in 2019-2021
You may not qualify if:
- General EDs not providing emergency care to children aged 0-18 years during the study period.
- General EDs with no baseline WPRS
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Manitobalead
- Manitoba Medical Service Foundationcollaborator
- Children's Hospital Research Institute of Manitobacollaborator
- AstraZenecacollaborator
Study Sites (1)
University of Manitoba
Winnipeg, Manitoba, R3E 3P4, Canada
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, INVESTIGATOR
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
October 11, 2023
First Posted
February 14, 2024
Study Start
October 2, 2022
Primary Completion
May 31, 2025
Study Completion
May 31, 2025
Last Updated
June 13, 2025
Record last verified: 2025-06