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Behavioral Treatments for Acute Stress Disorder In Firefighters

Developing Group Treatments for Acute Stress Disorder

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00183508
Enrollment
169
Registered
2005-09-16
Start date
Unknown
Completion date
2009-05-31
Last updated
2015-12-14

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

Conditions

Stress Disorders, Post-Traumatic

Keywords

PTSD, Occupational Health, Trauma, Job, CBT

Brief summary

This study will develop a treatment for firefighters experiencing symptoms of acute stress disorder (ASD). Effective treatments may reduce immediate symptoms and prevent the development of more chronic conditions, such as post-traumatic stress disorder (PTSD).

Detailed description

Exposure to traumatic events has reached unprecedented proportions in American society, and the rates of PTSD have risen significantly, particularly among populations with repetitive exposure to critical incidents. The continued threat of attacks against Americans warrants development of preventive interventions to reduce the occurrence of PTSD and its precursor, ASD. This study will determine the effectiveness of a preventive treatment in urban firefighters who have experienced a traumatic event. Firefighters will undergo an initial assessment that will include an interview and self-report questionnaires to measure depression, anxiety, coping skills, social support, physical health, and work functioning. Following the occurrence of a traumatic work-related event, firefighters will be reassessed. The post-incident assessment will consist of self-report questionnaires that assess ASD symptoms. Participants who display ASD symptoms will be randomly assigned to one of two groups: the first group will learn cognitive behavioral strategies for symptom reduction, and the second group will receive psychoeducation regarding common reactions to traumatic events. Participants' treatment will last for 12 weeks. Participants will have follow-up assessments 1 and 3 months after the interventional part of the study. Assessments will include clinical scales and interviews.

Interventions

BEHAVIORALCognitive behavioral therapy

Participants will learn cognitive behavioral strategies for symptom reduction

BEHAVIORALPsychoeducation

Participants will receive psychoeducation regarding common reactions to traumatic events

Sponsors

National Institute of Mental Health (NIMH)
CollaboratorNIH
Boston University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
21 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Currently an active duty, nonofficer member of a Boston area fire department * Willing and able to comply with all study requirements

Exclusion criteria

* Pregnancy or plan to become pregnant during the study * Plan to relocate within 2 months of study entry * Psychotic symptoms within 30 days prior to study entry * Experiencing severe depression at study entry OR having suicidal thoughts within 30 days prior to study entry * Evidence of severe organic impairment that would interfere with participation in the study * Current alcohol or substance dependence * Currently awaiting outcome of a court case involving exposure to traumatic events through the fire department

Design outcomes

Primary

MeasureTime frame
Accute stress disorder symptomsMeasured pre- and post-treatment and at follow-up assessments 1 and 3 months after the intervention

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026