Triage Assessment and NEWS-score as Risk Predictor in Older Frailty Adults in the ED

January 29, 2022 updated by: Janne Alakare, Helsinki University Central Hospital

3-level Triage Assessment and National Early Warning Score as Predictor for Mortality, Hospital Admission and ED Readmission for Older Frailty Patients in the ED

Emergency Department Triage Systems have not been shown to sufficiently recognize frail elderly patients in need of urgent assessment and care. In this prospective, observational study the performance of the 3-level triage system and the National Early Warning Score (NEWS) 2 are assessed (separately and combined) for predicting adverse outcomes in older frailty patients visiting in the ED. Observational data for this study is gathered as part of GAOPS - main study (ClinicalTrials.gov Identifier: NCT03751319).

Study Overview

Status

Completed

Conditions

Study Type

Observational

Enrollment (Actual)

1711

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Espoo, Finland, 02740
        • Helsinki University Central Hospital, Jorvi

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

75 years and older (Older Adult)

Accepts Healthy Volunteers

N/A

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Residents of aforementioned counties, aged over 75 years, who attend the Emergency department and have clinical frailty scale minimum 4.

Description

Inclusion Criteria:

  • "Clinical Frailty Scale" minimum 4 estimated at the arrival to the ED by nurse

Exclusion Criteria:

• Non-resident of the counties (City of Espoo, Kirkkonummi, Kauniainen) of the hospital district.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Older Adult Patients
ED patients age of ≥ 75 who have nurse assessed Clinical Frailty Scale ≥ 4.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Mortality
Time Frame: 30 days
Mortality during the 30 day follow-up
30 days

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Hospital admission
Time Frame: Day 0
Admission to hospital from the Emergency Department
Day 0
ICU/HDU admission
Time Frame: Day 0
Admission to the Intensive Care Unit or High Dependency Unit from the Emergency Department
Day 0
Readmission in the ED
Time Frame: Hour 72, Day 30
Re-visits to the ED after the index-visit
Hour 72, Day 30

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Veli-Pekka Harjola, Department of Emergency Medicine and Services, Helsinki University Hospital
  • Principal Investigator: Janne Alakare, MD, Department of Emergency Medicine and Services, Helsinki University Hospital

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Helpful Links

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 11, 2018

Primary Completion (Actual)

September 1, 2019

Study Completion (Actual)

October 28, 2020

Study Registration Dates

First Submitted

December 19, 2018

First Submitted That Met QC Criteria

December 19, 2018

First Posted (Actual)

December 20, 2018

Study Record Updates

Last Update Posted (Actual)

February 1, 2022

Last Update Submitted That Met QC Criteria

January 29, 2022

Last Verified

January 1, 2022

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • HUS/278/2018

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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