HFR-Fribourg
Fribourg, Canton of Fribourg, 1700, Switzerland
NCT Number: NCT06971419
Emergency department (ED) overcrowding is a growing issue, affecting patient safety, healthcare quality, and hospital efficiency. One strategy to manage low-acuity patients is triage-based redirection, where patients with non-urgent conditions are offered the option to receive care at external medical facilities instead of the ED.
This monocentric, prospective observational study will be conducted at Fribourg Cantonal Hospital, Switzerland, and evaluates the impact of a new electronic triage and redirection system (Logibec Réorientation). The study compares two triage processes:
Current practice - Redirection based on the Swiss Emergency Triage Scale (SETS), limited to low-acuity patients (SETS 4).
New practice - Redirection using the Logibec software, allowing redirection of both low-acuity (SETS 4) and semi-urgent (SETS 3) patients based on predefined criteria.
The primary objective is to assess whether the new triage-based redirection reduces the number of ED consultations per patient within 48 hours of their initial visit.
Secondary outcomes include:
Number of consultations in the ED or other medical facilities within 7 days Rate of hospital admissions within 7 days Patient satisfaction with redirection Evolution of health literacy over 6 months Number of ED visits over 6 months Participants are adult patients (≥18 years old) classified as SETS 3-4 and identified as eligible for redirection by the Logibec software. Data will be collected through phone interviews and questionnaires over a 6-month follow-up period.
This study aims to improve triage efficiency, patient flow management, and healthcare accessibility, while ensuring patient safety in the redirection process.
Trial opening soon.
Get Notified18 year and older
All sexes
Observational
Fribourg, Canton of Fribourg, 1700, Switzerland
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Name: Logibec Réorientation software-assisted triage and redirection
Type: Decision support system for emergency triage
Implementation:
Comparator: Standard nurse-led triage and redirection based only on the Swiss Emergency Triage Scale (SETS)
Key Distinction:
Time frame: From initial emergency department visit to 48 hours post-visit
This measure refers to the total number of emergency department (ED) visits per patient within 48 hours following their initial presentation to the ED.
The first consultation at the ED is counted as the initial visit.
This outcome aims to assess whether electronic triage-assisted redirection is effective, by providing service through alternative health care providers ,without patients needing further ED care
Time frame: From initial emergency department visit to 7 days post-visit
Time frame: From initial emergency department visit to 7 days post-visit
Time frame: At day 2 and day 7 post-visit
Patient satisfaction as assessed by satisfaction questionnaire
Time frame: From initial emergency department visit to 6 month post-visit
Time frame: At day 7 post-visit and 6 months post-visit
Health literacy as evaluated by EU-HLS-Q16 questionnaire
Contact information is provided by the study sponsor or research team.
Ludovic Galofaro, MD
CONTACT
Youcef Guechi, MD
CONTACT
Hôpital Fribourgeois
Other
FOllow-Up of LOW-Acuity Patients After REdirection From the Emergency Department at Fribourg Cantonal Hospital in Switzerland Using an Electronic TRIage Application: a Monocentric, Prospective Observational Study
Acronym: FO-LOW-RETRI
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07725965
Clinical Decision Support, Emergency Care
Cologne, Germany
View Trial DetailsNCT06034184
Learning, Mass Casualty Incident
Stockholm, Stockholm County, Sweden
View Trial DetailsNCT07312968
Triage
Catanzaro, Italy
View Trial DetailsNCT06666647
Emergency Medical Services, Intensive Care Patients Invasively Ventilated
Odense, Denmark
View Trial Details