Prevention of Health Care Workers* Health Problems after Work Related Critical Incidents: A Randomized Controlled Trial

Recruiting

• Conditions: 10002861; burnout; acute stress; traumatic stress / long-term exhaustion; vital exhaustion

• Registration Number: NL-OMON33841
• Lead Sponsor: Erasmus MC, Universitair Medisch Centrum Rotterdam

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 13 May 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: 180

Inclusion Criteria

Meeting with a work-related critical incident (critical incidents will be further defined after a first inventarisation in the in D3 mentioned wards)
Working in the present ward for at least 6 months at T0

Exclusion Criteria

Current serious psychiatric disorder, that needs treatment before any other intervention could be applied
Currently under treatment for any psychiatric problem

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Main study parameters: The main study parameters are the incidence of symptoms<br /><br>of Post Traumatic Stress Disorder, Burnout and Absenteeism four weeks post<br /><br>incident. </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Secondary endpoint is the score on the Trauma Screening Questionnaire two weeks<br /><br>post incident.</p><br>