NCT05388292

Brief Summary

The objective of this study is to design a computer-based Decision Support System (DSS) using the ESI (Emergency Severity Index) and ATS (Australasian Triage Scale) algorithms, integrate it into the Hospital Information Management System (HIMS), evaluate the effect of the triage management in the emergency department and ensure the continuity of the system.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
5,038

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Jul 2020

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

Study Start

First participant enrolled

July 16, 2020

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 16, 2020

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 16, 2020

Completed
1.6 years until next milestone

First Submitted

Initial submission to the registry

April 28, 2022

Completed
26 days until next milestone

First Posted

Study publicly available on registry

May 24, 2022

Completed
Last Updated

February 2, 2024

Status Verified

February 1, 2024

Enrollment Period

2 months

First QC Date

April 28, 2022

Last Update Submit

February 1, 2024

Conditions

Outcome Measures

Primary Outcomes (1)

  • Emergency Triage Decision Support System triage management was evaluated against the accuracy and duration of triage decisions

    The effect of the decision support system on the triage decision accuracy

    8 weeks (triage decision' accuracy in eight-week hospital information management system data)

Secondary Outcomes (1)

  • Emergency Triage Decision Support System

    8 weeks (triage decision' duration in eight-week hospital information management system data)

Study Arms (1)

Development of triage decision support system

OTHER

This is a quasi-experimental study with a single-group pre-test and post-test design. The study consisted of three stages. In the first stage, a structured Query Language Script was developed to evaluate the accuracy and duration of pre-and post-DSS triage decisions. In the second stage (pre-test), the accuracy and duration of pre-DSS triage decisions were evaluated. In the second stage, a DSS was prepared with rule-based decision trees method using the ESI and ATS algorithms and was integrated into the HIMS. In the third and last stage (post-test), the effect of the developed Emergency Triage Decision Support System on triage management was evaluated against the accuracy and duration of triage decisions.

Other: Emergency triage decision support system

Interventions

Evaluating the impact of the developed Emergency Triage Decision Support System on triage management

Development of triage decision support system

Eligibility Criteria

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

You may qualify if:

  • Data of adult patients who applied to the adult emergency department and whose triage record was opened by a triage nurse.
  • Patient data with no probable or definitive diagnosis of COVID-19.

You may not qualify if:

  • Data of pediatric trauma patients (under 18 years of age) Patient data for which the triage record was opened by non-nursing healthcare professionals Patient data recorded in triage by nurses who did not receive ATKDS, Emergency nurse triage, ESI, ATS training Data of patients who applied with a probable/definite diagnosis of COVID-19 and underwent PCR testing Patient data in the date range when extraordinary changes were made in the adult emergency department patient triage area and evaluation process due to the COVID 19 pandemic and the developed system could not be used (must use the SB COVID Algorithm)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Akdeniz University

Antalya, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Emergencies

Condition Hierarchy (Ancestors)

Disease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Fatma Cebeci

    1962

    STUDY CHAIR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Masking Details
This is a quasi-experimental study with a single-group pre-test and post-test design.
Purpose
PREVENTION
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

April 28, 2022

First Posted

May 24, 2022

Study Start

July 16, 2020

Primary Completion

September 16, 2020

Study Completion

September 16, 2020

Last Updated

February 2, 2024

Record last verified: 2024-02

Data Sharing

IPD Sharing
Will not share

Locations