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Firefighters Accessing Care for Trauma: A Clinical Case Series of Distance NET for PTSD/I Symptoms

Firefighters Accessing Care for Trauma: A Clinical Case Series Testing the Efficacy of Distance-Delivered Narrative Exposure Therapy in Reducing PTSD/I Symptoms

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04386330
Enrollment
19
Registered
2020-05-13
Start date
2020-06-29
Completion date
2021-12-31
Last updated
2022-03-31

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

Conditions

Post Traumatic Stress Disorder, Post Traumatic Stress Injury

Brief summary

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.

Interventions

BEHAVIORALDistance-delivered NET

One-on-one intervention delivered by a paraprofessional; 12 weekly videoconference sessions at 90 minutes.

Sponsors

Canadian Institutes of Health Research (CIHR)
CollaboratorOTHER_GOV
University of New Brunswick
CollaboratorOTHER
IWK Health Centre
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Participants must meet the following criteria to be eligible to move on to Consent 1. Be at least 19 years of age 2. Be able to understand spoken and written English at a Grade 8 level 3. Be employed, or have been employed, by the fire service or be current or past fire service volunteers. 4. Fulfill the criteria of full or subclinical PTSD/I according to the PCL-5. 5. Have access to a computer with Internet. 6. Live in Atlantic Canada or Ontario. 7. Consent to be audio- (for consent and interview) and video-recorded (for intervention sessions).

Exclusion criteria

1. Having a psychotropic medication change in the past three weeks. 2. Are currently engaged in or have previously been engaged in exposure therapy for PTSD/I. 3. Meet criteria for current mania or psychosis. 4. Endorse suicidal ideation with plan or intent. 5. Experience high levels of dissociation (as assessed by a score of \>18.5 on the Shutdown Dissociation Scale).

Design outcomes

Primary

MeasureTime frameDescription
Change in PTSD/I symptomsBaseline, Immediately Post- intervention, 2 month follow up, 6 month follow upPTSD/I symptoms are measured with the PTSD Checklist - 5 (PCL-5)
Change in depressive symptomsBaseline,Immediately Post-intervention, 2 month follow up, 6 month follow upDepression symptoms will be measured using the Patient Health Questionnaire (PHQ-9)
DisabilityBaseline, Immediately Post-intervention, 2 month follow up, 6 month follow upDisability will be measured with the Sheehan Disability Scale

Secondary

MeasureTime frameDescription
Recruitment RatesBaselineRecruitment rates will be tracked by research staff throughout the study
Intervention AdherenceImmediately Post-InterventionIntervention 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.
Anxiety SymptomsBaseline, Immediately Post-intervention, 2 month follow up, 6 month follow upAnxiety symptoms will be measured using the Generalized Anxiety Disorder - 7 item (GAD-7)
Intervention Perceptions and SatisfactionImmediately Post-InterventionIntervention perceptions and satisfaction will be measured via open-ended questions administered through a post-intervention interview
Coach AllianceImmediately Post-InterventionCoach alliance will be measured using the Working Alliance Inventory - Short Form Revised (WAI-SR)
Physical HealthBaseline, Immediately Post-intervention, 2 month follow up, 6 month follow upPhysical health will be measured with the Patient Health Questionnaire Physical Symptoms (PHQ-15)
Health Service UseBaseline, Immediately Post-intervention, 2 month follow up, 6 month follow upHealth 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

Countries

Canada

Outcome results

None listed

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