Digital Anticipatory Protocols at Triage to Improve ED Flow.

Recruiting Observational Study
Length of Stay Emergency Department Crowding Emergency Department Patient Emergency Department Triage Nurses Workflow Diagnostic Tests
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
15,500 (estimated)
Sponsor
Hôpital Fribourgeois · Other
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About This Trial
This study aims to evaluate a pre-post intervention adding an early management decision at the end of the triage process to improve patient throughput. The intervention consists of adding digital checkboxes to the electronic triage system, providing nurses with formalized options for anticipated management based on patient acuity. The study compares a pre-intervention phase (May 1st to July 31st, …
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * All patients over 18 years who registered at the admission desk during the study period. Exclusion Criteria: * Arrival by emergency medical services (ambulance or helicopter) * Patient trajectory bypassing the standard nurse-led triage process * Patient directly referred to …
Contacts

Thomas Castelain

+41263061392

thomas.castelain@h-fr.ch

CONTACT

Youcef Guechi

+41263063142

youcef.guechi@h-fr.ch

CONTACT