- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03842553
Posttraumatic Stress Symptoms Among Rescuers at Risk
Rescuers at Risk: Posttraumatic Stress Symptoms Differ Among Police Officers, Fire Fighters, Ambulance Personnel, and Emergency and Psychiatric Nurses
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
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Bern, Switzerland, 3000
- University Hospital of Psychiatry, University of Bern
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Employees of rescue and emergency services in the canton Bern, Switzerland: - Firefighters of the canton Bern
- Ambulance personnel of the canton Bern
- Police officers of the canton Bern
- Emergency nurses of the University Hospital of Bern
- Psychiatric nurses of University Hospital of Psychiatry, Bern
Description
Inclusion Criteria:
Employee at the rescue or emergency services. The participation in the anonymous online study is voluntary and promoted by the department heads at the places of work corresponding to the studied professions. No ethical approval is needed as the survey was voluntary and anonymous and participants gave consent to use the data with their participation.
Exclusion Criteria:
- None
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Police officers
Police officers from the cantonal police forces in Bern, Switzerland
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|
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Firefighters
Firefighters from the professional fire service of the Canton Bern, Switzerland
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|
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Ambulance personnel
Ambulance personnel of the Canton Bern, Switzerland
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|
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Emergency nurses
Emergency nurses of the Emergency Unit of the University Hospital of Bern, Switzerland
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|
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Psychiatric nurses
Psychiatric nurses of the University Hospital of Psychiatry, University of Bern, Switzerland
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
PTSS-10
Time Frame: at baseline
|
Posttraumatic Stress Symptoms assessed with the Post Traumatic Symptom Scale, a self-rating scale used in screening and follow-up studies on catastrophe that measures the most common posttraumatic symptoms (sleep disorders, nightmares, fear of reminders, etc.)
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at baseline
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Well-being
Time Frame: at baseline
|
Mental well-being assessed with the German version of the shortest General Health Questionnaire 12 (GHQ-12).
Psychological distress and psychiatric disorders were assessed with the German Version of the Brief Symptom Inventory (BSI).
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at baseline
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Suicidal Ideation
Time Frame: within the last 12 months before the survey
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Participants were asked if they had suicidal ideation in the 12 months prior to the questionnaire
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within the last 12 months before the survey
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Psychological distress and psychiatric disorders
Time Frame: at baseline
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German Version of the Brief Symptom Inventory (BSI).
The 53-item self-report questionnaire measures symptoms of general psychopathology.
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at baseline
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Self-efficacy
Time Frame: at baseline
|
Self-efficacy was measured using the General Perceived Self-Efficacy Scale, a 10-item self-report instrument for personality diagnostics based on Banduras's concept of perceived self-efficacy that measures the general optimistic competence expectation
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at baseline
|
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Coping Strategies
Time Frame: at baseline
|
5-point Likert scale, ranging from a score of 1, indicating "not helpful"; to 5, "very helpful."
According to the operationalization of Coolidge, coping strategies were divided into three main subscales: I) problem-focused coping strategies, which was comprised of the subscales of "instrumental support" (getting help and advice from psychologic professionals) and "active job coping" (debriefing with operation team, supervisor, and work colleagues); II) dysfunctional coping strategies, which included "substance use" (alcohol or medication), "avoidance" (avoidance of situations and emotions associated with the stressful/traumatic situation), and "self-distraction" (turning to work or other activities to take the mind off the stressful situation); III) emotion-focused coping strategy (humor, getting emotional support from close friends, thinking about the positive aspects of the job).
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at baseline
|
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The burden of stressful job-related circumstances
Time Frame: at baseline
|
The burden of stressful job-related circumstances, such as dealing with situations including people (aggressive and violent people, dealing with deaths or suicide, threats, dealing with relatives, involvement of children) and job-related conditions (incorrect or wrong information about the emergency situation, shift work, time pressure).
Participants stated if they had ever experienced a presented situation, and if so, whether the situation caused a light or heavy stress burden.
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at baseline
|
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work-unrelated trauma
Time Frame: at baseline
|
Number of previous experienced work-unrelated trauma
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at baseline
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work-related trauma
Time Frame: at baseline
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Number of experienced trauma at work
|
at baseline
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Leila Soravia, Ph.D., University Hospital of Psychiatry, University of Bern
Publications and helpful links
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- PTSD2014
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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