University of New Brunswick
Fredericton, New Brunswick, E3B5A3, Canada
NCT Number: NCT04386330
Repeated exposure to trauma is an unavoidable part of the job for firefighters. Because of this, many Canadian firefighters screen positive for posttraumatic stress disorder/injury (PTSD/I). Unfortunately, like the general population, firefighters face many barriers to accessing mental health care. As a result, additional efforts are needed to increase timely access to effective PTSD/I services that are delivered in a way that reduces confidentiality and stigma risk.
This research study will test the preliminary efficacy and feasibility of distance-delivered Narrative Exposure Therapy (NET) delivered by a paraprofessional for firefighters with PTSD/I. NET is an evidence-based intervention approach developed specifically for PTSD/I resulting from repeated and continuous trauma. The intervention will be conducted via videoconference with a trained paraprofessional supervised by a clinical psychologist. The NET intervention will consist of 12 weekly 90-minute videoconference sessions.
Approximately 25 firefighters will be recruited to participate in the study. To test the efficacy of the intervention, participants will complete self-report questionnaires about PTSD/I and other mental health symptoms pre- and post-intervention as well as two- and six-months following intervention completion. Participants will also complete an open-ended interview at the end of the intervention to assess feasibility and participant satisfaction.
Looking for future studies?
Notify Me19 year and older
All sexes
Interventional
Not applicable
Fredericton, New Brunswick, E3B5A3, Canada
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Participants must meet the following criteria to be eligible to move on to Consent
Exclusion criteria
One-on-one intervention delivered by a paraprofessional; 12 weekly videoconference sessions at 90 minutes.
Time frame: Baseline, Immediately Post- intervention, 2 month follow up, 6 month follow up
PTSD/I symptoms are measured with the PTSD Checklist - 5 (PCL-5)
Time frame: Baseline,Immediately Post-intervention, 2 month follow up, 6 month follow up
Depression symptoms will be measured using the Patient Health Questionnaire (PHQ-9)
Time frame: Baseline, Immediately Post-intervention, 2 month follow up, 6 month follow up
Disability will be measured with the Sheehan Disability Scale
Time frame: Baseline, Immediately Post-intervention, 2 month follow up, 6 month follow up
Anxiety symptoms will be measured using the Generalized Anxiety Disorder - 7 item (GAD-7)
Time frame: Baseline, Immediately Post-intervention, 2 month follow up, 6 month follow up
Physical health will be measured with the Patient Health Questionnaire Physical Symptoms (PHQ-15)
Time frame: Baseline, Immediately Post-intervention, 2 month follow up, 6 month follow up
Health service use will be measured using a series of questions regarding participant's use of health services as well as frequency and intensity of service use
Time frame: Baseline
Recruitment rates will be tracked by research staff throughout the study
Time frame: Immediately Post-Intervention
Intervention adherence will be measured via attendance records of participants kept by their coach. These attendance records will be used to measure the average number of completed sessions and the percentage of participants who did not complete the intervention.
Time frame: Immediately Post-Intervention
Coach alliance will be measured using the Working Alliance Inventory - Short Form Revised (WAI-SR)
Time frame: Immediately Post-Intervention
Intervention perceptions and satisfaction will be measured via open-ended questions administered through a post-intervention interview
IWK Health Centre
Other
Firefighters Accessing Care for Trauma: A Clinical Case Series Testing the Efficacy of Distance-Delivered Narrative Exposure Therapy in Reducing PTSD/I Symptoms
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT04385927
Mental Disorders, Post Traumatic Stress Disorder
Halifax, Nova Scotia, Canada
View Trial DetailsNCT07737652
Anxiety, Anxiety Disorders
Tuscaloosa, Alabama, United States
View Trial DetailsNCT06868446
Mental Disorders, PTSD
Tallahassee, Florida, United States
View Trial DetailsNCT04888169
Mental Disorders, Post Traumatic Stress Disorder
San Francisco, California, United States
View Trial Details