Impact of the Qatar 2022 FIFA World Cup on PED Use and Misuse Patterns
The Impact of the Qatar 2022 FIFA World Cup During Winter Epidemics on Paediatric Emergency Department Use and Misuse Patterns: a Multicentre, Retrospective, Population-based Study
1 other identifier
observational
18,000
1 country
1
Brief Summary
A retrospective cohort study to explore the impact of the FIFA World Cup 2022 Qatar on paediatric emergency department attendance at two tertiary centres during unprecedent winter viral epidemics.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Sep 2021
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
September 1, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 20, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
January 20, 2023
CompletedFirst Submitted
Initial submission to the registry
April 5, 2023
CompletedFirst Posted
Study publicly available on registry
April 18, 2023
CompletedApril 18, 2023
April 1, 2023
1.4 years
April 5, 2023
April 5, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
PED visits
Retrospective analysis of number of PED visits (counts).
Institutional electronic medical records analysed retrospectively from October 1st, 2022 to December 31, 2022
Secondary Outcomes (7)
Triage acuity score
Institutional electronic medical records analysed retrospectively from October 1st, 2022 to December 31, 2022
Chief complaint
Institutional electronic medical records analysed retrospectively from October 1st, 2022 to December 31, 2022
Main diagnosis
Institutional electronic medical records analysed retrospectively from October 1st, 2022 to December 31, 2022
Audience
Analysed retrospectively from October 1st, 2022 to December 31, 2022
RSV incidence
Analysed retrospectively from October 1st, 2022 to December 31, 2022
- +2 more secondary outcomes
Study Arms (1)
All participants
Data from electronic medical records of all patients under 16 years of age with medical, surgical and traumatology emergencies attending the paediatric emergency departments during the study period
Interventions
Eligibility Criteria
All patients under 16 years of age with medical, surgical and traumatology emergencies attending each pediatric emergency department during the study period will be included. This also includes transfer cases from other hospitals, as well as those who leave prematurely without being seen.
You may qualify if:
- all patients
You may not qualify if:
- none
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Geneva Children's Hospital
Geneva, Switzerland
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Johan N Siebert, MD
Geneva Children's Hospital, Geneva University Hospitals, Geneva, Switzerland
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
April 5, 2023
First Posted
April 18, 2023
Study Start
September 1, 2021
Primary Completion
January 20, 2023
Study Completion
January 20, 2023
Last Updated
April 18, 2023
Record last verified: 2023-04
Data Sharing
- IPD Sharing
- Will share
- Time Frame
- Available from 6 month to 5 years after trial publication.
- Access Criteria
- * Data will be made available from the corresponding author upon approval of a proposal and with a signed data access agreement. * Data will be made available for a specified research purpose. * The request proposal must include a statistician.
Individual Participant Data will be deidentified and the study investigators will house the data locally on secured servers at the Geneva University Hospitals. The datasets used or analysed during the current trial will be available from the corresponding author upon reasonable request. Only deidentified/anonymised data will be shared.