Evaluation of Emergency Department (ED) Staff Stress Level During COVID-19 Pandemic

NCT04383886 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 247

Last updated 2023-04-06

No results posted yet for this study

Summary

In the context of the COVID-19 pandemic, Emergency Department (ED) are in front line for the reception of patients presenting COVID-19 symptoms and have to face a new situation given the expected number of patients. Staff participate in suspect patients triage, in the diagnosis and the management of Covid-19 patients, having to follow the instructions and recommendations that evolve in real time, depending on the stage, resources and means available. This situation requires that the staff immediately adaptation within this reorganization and redeployment of the activity. Then; they are subject to many stress and anxiety factors such as:

* Increased activity: massive influx of patients, overload of work, lack of material and human resources
* Modification of practices: training in procedures, measures isolation and prevention of contamination of other patients, replacement by professionals reassigned from other departments
* Ethical dilemma: decisions to be made in an emergency, patient prioritization
* Numerous, evolving information, from various sources and sometimes contradictory (national, governance, service, media)
* Individual: fear of personal contamination and of those close to you, personal organization in a situation of confinement of the population, loss of usual social support
* Anxiety and stress management of patients and relatives, their entourage and colleagues In this study, it is proposed to study the psychic impact of the COVID-19 pandemic on emergency department staff.

Conditions

  • Emergency Department Staff During the COVID-19 Pandemic
  • Emergency Department Staff's Level of Stress

Interventions

OTHER

stress and anxiety questionnaire

Emergency department staff will be asked to fill in questionnaires in order to measure their stress and anxiety level, their propensity to have a burn-out, their consumption of psychoactive substances such as alcohol, tobacco, coffee or anxiolytic, their sleep disorder.

Sponsors & Collaborators

  • Hospices Civils de Lyon

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-04-18
Primary Completion
2020-09-12
Completion
2020-09-12

Countries

  • France

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04383886 on ClinicalTrials.gov