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Clinical Trials/NCT07436052
NCT07436052CompletedNot Applicable

Impact on Triage Performance in Simulated Multiple-casualty Situations of TST (Ten Second Triage) Versus Sieve

Stuby Loric1 site in 1 country201 target enrollmentStarted: February 13, 2026Last updated:
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
201
Locations
1
Primary Endpoint
Triage accuracy (triage score)

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
Triple (Participant, Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • 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

Exclusion Criteria

  • 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

Arms & Interventions

Sieve

Active Comparator

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

Intervention: Sieve triage algorithm (Other)

TST

Experimental

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

Intervention: Ten Second Triage algorithm (Other)

Outcomes

Primary Outcomes

Triage accuracy (triage score)

Time Frame: Through study completion, an average of 1 hour

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.

Secondary Outcomes

  • 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)

Investigators

Sponsor
Stuby Loric
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Stuby Loric

Principal Investigator

Geneve TEAM Ambulances

Study Sites (1)

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