The Burnout Syndrome in Emergency Department Triage Nurses (BurN_ED)

August 6, 2018 updated by: Eugenia-Maria Muresan, Iuliu Hatieganu University of Medicine and Pharmacy

Sindromul de Burnout la asistenții Medicali de Triaj Din unitățile de Primire urgențe

Assessment of burnout syndrome of triage nurses from Emergency Departments from Cluj-Napoca, Romania.

Study Overview

Detailed Description

This study is aiming at assessing the burnout syndrome amongst triage nurses working in the Emergency Departments in Cluj-Napoca. The study design is observational, prospective and multicentric.

At this moment, there are 43 nurses covering triage shifts in the Emergency Clincial County Hospital Cluj and 18 more within Emergency Clinical Hospital for Children Cluj-Napoca. On average, these ED roughly attend 90.000 patients yearly.

Questionnaires are based on Copenhagen Burnout Inventory, with additional clinical cases that require triage coding according to The Romanian National Triage Protocol of 2016. Each triage nurse will complete the questionnaire when beginning the triage shift and after a period of 2, 4 or 6 hours.

Study Type

Observational

Enrollment (Actual)

56

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

    • Cluj
      • Cluj-Napoca, Cluj, Romania, 400001
        • Emergency County Hospital for Children
      • Cluj-Napoca, Cluj, Romania, 400554
        • Emergency Clinical County Hospital Cluj-Napoca - Emergency Department

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Emergency Department nurses from Emergency Clinical County Hospital Cluj and Emergency Clinic Hospital for Children Cluj-Napoca.

Description

Inclusion Criteria:

  • ED nurse within Emergency Clinical County Hospital Cluj and Emergency Clinic Hospital for Children Cluj-Napoca.

Exclusion Criteria:

  • triage experience of at least 1 year

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

  • Observational Models: Cohort
  • Time Perspectives: Prospective

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
2h assessment
The assessment of the burnout syndrome will be carried out at the beginning of the triage shift and after 2 hours.

A questionnaire based on Copenhagen Burnout Inventory will be completed by each participant to the study, at the beginning of the triage shift and after 2, 4 or 6 hours.

The questionnaire also contains clinical cases that require triage coding.

The triage scores of the first 5 and the last 5 cases assessed by the investigated nurse will be compared with the triage codes of an expert evaluator (nurse involved in designing The National triage Protocol).
4h assessment
The assessment of the burnout syndrome will be carried out at the beginning of the triage shift and after 4 hours.

A questionnaire based on Copenhagen Burnout Inventory will be completed by each participant to the study, at the beginning of the triage shift and after 2, 4 or 6 hours.

The questionnaire also contains clinical cases that require triage coding.

The triage scores of the first 5 and the last 5 cases assessed by the investigated nurse will be compared with the triage codes of an expert evaluator (nurse involved in designing The National triage Protocol).
6h assessment
The assessment of the burnout syndrome will be carried out at the beginning of the triage shift and after 6 hours.

A questionnaire based on Copenhagen Burnout Inventory will be completed by each participant to the study, at the beginning of the triage shift and after 2, 4 or 6 hours.

The questionnaire also contains clinical cases that require triage coding.

The triage scores of the first 5 and the last 5 cases assessed by the investigated nurse will be compared with the triage codes of an expert evaluator (nurse involved in designing The National triage Protocol).

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Assessment of burnout syndrome in triage ED nurses
Time Frame: 2 to 6 hours
Copenhagen Burnout Inventory
2 to 6 hours

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Efficacy of triage ED nurses
Time Frame: 2 to 6 hours
The triage scores of the first 5 and the last 5 cases assessed by the investigated nurse will be compared with the diagnostic codes of the physicians who treated those patients.
2 to 6 hours

Collaborators and Investigators

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

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)

April 15, 2017

Primary Completion (Actual)

June 15, 2017

Study Completion (Actual)

September 30, 2017

Study Registration Dates

First Submitted

April 7, 2017

First Submitted That Met QC Criteria

April 7, 2017

First Posted (Actual)

April 12, 2017

Study Record Updates

Last Update Posted (Actual)

August 7, 2018

Last Update Submitted That Met QC Criteria

August 6, 2018

Last Verified

August 1, 2018

More Information

Terms related to this study

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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