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

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

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON33841

Enrollment

180

Registered

2009-03-06

Start date

2009-05-25

Completion date

Unknown

Last updated

2024-05-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

burnout acute stress traumatic stress / long-term exhaustion vital exhaustion

Interventions

The Controlgroup receives a *placebo* intervention (watchful waiting). Interventiongroup-1 receives watchful waiting + psycho-education. Interventiongroup-2 receives watchful waiting + psycho-educat

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

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

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

Design outcomes

Primary

Measure	Time frame
Main study parameters: The main study parameters are the incidence of symptoms of Post Traumatic Stress Disorder, Burnout and Absenteeism four weeks post incident.	—

Secondary

Measure	Time frame
Secondary endpoint is the score on the Trauma Screening Questionnaire two weeks post incident.	—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)