- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03110536
The Burnout Syndrome in Emergency Department Triage Nurses (BurN_ED)
Sindromul de Burnout la asistenții Medicali de Triaj Din unitățile de Primire urgențe
Study Overview
Status
Conditions
Intervention / Treatment
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
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Cluj
-
Cluj-Napoca, Cluj, Romania, 400001
- Emergency County Hospital for Children
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Cluj-Napoca, Cluj, Romania, 400554
- Emergency Clinical County Hospital Cluj-Napoca - Emergency Department
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
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
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
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 9253/11.04.2017
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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