NCT07436052

Brief Summary

This study will compare two emergency triage algorithm - Ten Second Triage (TST) versus Sieve - to see which one works better during simulated mass-casualty incidents. Triage is the process of quickly deciding which patients need immediate care when there are many injured people. Making fast and accurate decisions is essential in these situations. Ambulance professionals and students in French-speaking Switzerland will be invited to take part. Participants will be randomly assigned to use either the TST method or the Sieve method. After a short introduction to the assigned method, each participant will complete two computer-based simulation scenarios involving 17 injured patients each (one scenario with penetrating injuries and one with blunt injuries). The simulated patients' conditions will change over time, similar to real-life emergencies using a physiological validated simulator (HUMAn). The main goal is to measure how accurately participants identify patients who need immediate treatment. For each correct triage decision, participants receive one point. A total score will be calculated across both scenarios. If a sufficient sample size could be reached, a mixed effect logistic regression model will be generated to answer to research question. The study will also measure how long participants take to make triage decisions, how often patients are over-triaged or under-triaged, and how easy participants find the method to use. The results will help determine which triage method may be more effective for use by ambulance personnel during major incidents.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
201

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Feb 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

First Submitted

Initial submission to the registry

February 13, 2026

Completed
Same day until next milestone

Study Start

First participant enrolled

February 13, 2026

Completed
14 days until next milestone

First Posted

Study publicly available on registry

February 27, 2026

Completed
14 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 13, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 13, 2026

Completed
Last Updated

April 22, 2026

Status Verified

April 1, 2026

Enrollment Period

28 days

First QC Date

February 13, 2026

Last Update Submit

April 17, 2026

Conditions

Keywords

Mass casualty incidentSimulationRandomized controlled trialTriage accuracyEmergency medical services (EMS)Ten Second Triage (TST)Overtriage and undertriageBlunt and penetrating traumaSieveSimulation-basedMajor incident preparednessSimulation trainingDisaster medicineTriageTriage algorithmsPrehospital TriageEmergency Medical Services

Outcome Measures

Primary Outcomes (1)

  • Triage accuracy (triage score)

    Triage accuracy is defined as the proportion of correct triage decisions made by each participant across two simulated mass-casualty scenarios (34 patients in total). For each simulated patient, participants receive: 1 point for a correct triage decision (0 points for an incorrect decision). A triage decision is considered correct if the assigned priority category matches the simulated patient's expected clinical evolution based on the HUMAn dynamic simulation model (i.e., correct identification of patients requiring immediate treatment versus those who do not, including appropriate classification of deceased patients). The primary endpoint is the total triage score per participant (range 0-34), calculated by summing correct decisions across both scenarios.

    Through study completion, an average of 1 hour

Secondary Outcomes (4)

  • Triage duration

    Through study completion, an average of 1 hour

  • Overtriage rate

    Through study completion, an average of 1 hour

  • Undertriage rate

    Through study completion, an average of 1 hour

  • User satisfaction and perceived ease of use

    Through study completion, an average of 1 hour

Study Arms (2)

Sieve

ACTIVE COMPARATOR

The control group will be provided with the Sieve triage algorithm.

Other: Sieve triage algorithm

TST

EXPERIMENTAL

The experimental group will be provided with the Ten Seconde Triage algorithm

Other: Ten Second Triage algorithm

Interventions

Ten Second Triage (TST) is a rapid primary triage algorithm designed for use in mass-casualty incidents. It aims to allow rescuers to assess and categorize a patient in approximately 10 seconds based on a small number of immediately observable clinical signs. The algorithm focuses on key life-saving indicators such as ability to walk, presence of major external bleeding, airway status, breathing effectiveness, and level of consciousness. Based on these findings, patients are assigned to standard triage categories (e.g., immediate, urgent, delayed, or deceased). TST prioritizes speed and simplicity to support rapid decision-making when resources are limited and many victims require simultaneous assessment.

TST

Sieve (NARU) triage algorithm is a structured primary triage method used during mass-casualty incidents, developed and promoted by the National Ambulance Resilience Unit (NARU). It is designed to rapidly sort large numbers of patients based on simple physiological criteria. The Sieve algorithm follows a stepwise assessment focusing on the ability to walk, breathing status and rate, and circulation (including signs of life-threatening hemorrhage). Patients are then assigned to standard triage categories (immediate, urgent, delayed, or deceased). Sieve emphasizes consistency and reproducibility of triage decisions and is widely used in prehospital disaster response and training to support safe prioritization when resources are limited.

Sieve

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Prehospital care professionals (e.g., ambulance personnel) or paramedic students
  • Practicing or training in French-speaking Switzerland
  • Likely to be involved in the management of major incidents or mass-casualty events
  • Provided informed consent to participate

You may not qualify if:

  • Participants who answered "No" to the statement confirming that their questionnaire responses reflect their usual personal practice
  • Participants who did not view the instructional video of the assigned triage algorithm (time spent on the video page is recorded), except participants randomized to the Sieve arm who routinely use the Sieve algorithm in their clinical practice

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

École supérieure de soins ambulanciers (ESAMB)

Geneva, Canton of Geneva, 1213, Switzerland

Location

Study Officials

  • Loric Stuby

    Genève TEAM Ambulances

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
TRIPLE
Who Masked
PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

February 13, 2026

First Posted

February 27, 2026

Study Start

February 13, 2026

Primary Completion

March 13, 2026

Study Completion

March 13, 2026

Last Updated

April 22, 2026

Record last verified: 2026-04

Locations