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Medical Checklists in the Emergency Department

Not Applicable
Recruiting
Conditions
Emergencies
Tricyclic Antidepressant Toxicity
Tricyclic Antidepressant Poisoning
Registration Number
NCT05496114
Lead Sponsor
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Brief Summary

This study aims to investigate whether the use of medical checklists in the emergency department can decrease resuscitation time in critically ill patients.

Detailed Description

A scenario evaluating tricyclic antidepressant poisoning will be carried out with and without medical checklist access. Emergency physicians from the Netherlands who are willing to take part in the study are randomly allocated to perform the scenario with or without checklists.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
56
Inclusion Criteria
  • Emergency Physicians recognised by KNMG (Koninklijke Nederlandsche Maatschappij tot bevordering van de Geneeskunst) working in the Netherlands
Exclusion Criteria
  • Residents (in Dutch: AIOS) Emergency Medicine
  • Interns (in Dutch: ANIOS) Emergency Medicine

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Duration of the scenarioThrough study completion, indicated 10 months

The primary outcome is the duration of primary resuscitation utilizing the checklists versus treatment on discretion of the treating physician. The simulation will be terminated when all indicated interventions are performed, when the team expresses that they cannot think of any other intervention to perform or when 15 minutes have elapsed.

Secondary Outcome Measures
NameTimeMethod
Number of indicated interventions performed by the emergency physicianThrough study completion, indicated 10 months

Based on the checklist, a number of predefined indicated interventions is established. When reviewing the video recordings, it will be noted whether indicated interventions were performed and when these interventions were performed. The order according to which interventions are performed will not impact on this secondary outcome.

Satisfaction of emergency physicians with the checklistsThrough study completion, indicated 10 months

Participants, who run the scenarios with checklist access, will be asked to fill out a questionnaire evaluating the checklist (5-point Likert scales).

Trial Locations

Locations (1)

Amsterdam University Medical Center

🇳🇱

Amsterdam, Netherlands

Amsterdam University Medical Center
🇳🇱Amsterdam, Netherlands
Malu van der Capellen, MD
Contact
0031645144756
malucapellen@gmail.com
Maik Berendsen, MD
Contact
0031645556601
maik.berendsen@amsterdamumc.nl

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