Skip to main content
Clinical Trials/NCT03070249
NCT03070249CompletedNot Applicable

Compassion Fatigue Among Emergency Department Healthcare Providers

University of Florida1 site in 1 country100 target enrollmentStarted: April 13, 2017Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
100
Locations
1
Primary Endpoint
Assess Compassion Fatigue as precursory research

Study Overview

Brief Summary

This study will assess compassion fatigue among healthcare providers in a single emergency department (ED) using the Professional Quality of Life (ProQoL) scale.

Study Design

Study Type
Observational
Observational Model
Case Only
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Currently employed as a health care provider in the emergency department. All eligible individuals will be 18 years and older.

Exclusion Criteria

  • Individuals that are not currently employed in the emergency department

Outcomes

Primary Outcomes

Assess Compassion Fatigue as precursory research

Time Frame: Baseline

Professional Quality of Life Scale survey (PROQOL) assesses compassion satisfaction and compassion fatigue. 1=Never 2=Rarely 3=Sometimes 4=Often 5=Very Often

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

Loading locations...

Similar Trials

Compassion Fatigue in ED Providers | Clinical Trial