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NCT Number: NCT06971419

FOllow-up of LOW-acuity Patients After REdirection From a Swiss Emergency Department Using an Electronic TRIage Application

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥18 years old
  • Triage level SETS 3 or SETS 4 (classified as semi-urgent or low-acuity)
  • Identified as eligible for redirection by the Logibec electronic triage system
  • Able to speak and read French or German (for informed consent and follow-up)
  • Provides informed consent: Oral consent at Day 2 and Signed informed consent sent by post after inclusion

Exclusion criteria

  • Inability to provide informed consent (e.g., cognitive impairment, language barrier without translation support)
  • Inability to comply with study procedures, such as: Severe hearing impairment without hearing aids; Acute psychiatric conditions preventing participation; Not available for follow-up phone calls within the next 6 months

Treatment and study plan

intervention is the use of aTriage-Based Patient Redirection Using an Electronic Decision Support Toolin the emergency department (ED)

Other

Name: Logibec Réorientation software-assisted triage and redirection

Type: Decision support system for emergency triage

Implementation:

  • Applied during patient triage in the emergency department
  • Assists in identifying low-acuity (SETS 4) and semi-urgent (SETS 3) patients eligible for redirection
  • Uses standardized inclusion/exclusion criteria to guide redirection decisions

Comparator: Standard nurse-led triage and redirection based only on the Swiss Emergency Triage Scale (SETS)

Key Distinction:

  • The investigated group receives Logibec-assisted triage and redirection.
  • The comparator group follows traditional nurse-led triage without electronic support, limiting redirection to SETS 4 patients only.

Primary outcomes

  1. Number of Emergency Department Consultations per Patient Within 48 Hours After Initial Visit

    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.

    • Any subsequent unplanned return visits to the ED within 48 hours of the initial visit are included in the count.
    • Data collection is conducted through electronic health records (EHR) review and patient follow-up phone calls.

    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

Secondary outcomes

  1. the number of consultations per patient in the ED or other medical services within 7 days after the first ED visit

    Time frame: From initial emergency department visit to 7 days post-visit

  2. the proportion of patients who need hospitalization related to initial complaint within 7 days

    Time frame: From initial emergency department visit to 7 days post-visit

  3. the proportion of patients satisfied with the redirection process

    Time frame: At day 2 and day 7 post-visit

    Patient satisfaction as assessed by satisfaction questionnaire

  4. the mean number of ED consultations after 1 month, 3 months and 6 months per patient

    Time frame: From initial emergency department visit to 6 month post-visit

  5. the evaluation of the health literacy and its evolution within 6 months of visit

    Time frame: At day 7 post-visit and 6 months post-visit

    Health literacy as evaluated by EU-HLS-Q16 questionnaire

Study contacts

Contact information is provided by the study sponsor or research team.

Ludovic Galofaro, MD

CONTACT

[email protected]

+41263063112

Youcef Guechi, MD

CONTACT

[email protected]

+41263063112

Sponsors and collaborators

Lead sponsor

Hôpital Fribourgeois

Other

Collaborators

  • University of Fribourg

Registry information

Official study title

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

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
May 14, 2025
Registry last updated
May 14, 2025

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.

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