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An Efficient Treatment for Posttraumatic Injury for Firefighters

P

Palo Alto Veterans Institute for Research

Status

Enrolling

Conditions

Posttraumatic Stress Disorder
Insomnia
Nightmare

Treatments

Behavioral: Written Exposure Therapy (WET)
Behavioral: Cognitive Behavioral Therapy for Insomnia (CBTi)
Behavioral: Cognitive Behavioral Therapy for Nightmares (CBTn)
Behavioral: Waitlist

Study type

Interventional

Funder types

Other

Identifiers

NCT05950035
MCA0006AGG

Details and patient eligibility

About

The goal of this two-arm pilot randomized controlled trial is to test a behavioral intervention that integrates three evidence-based cognitive behavioral interventions (written exposure therapy; WET, cognitive behavioral therapy for insomnia; CBT-I, and cognitive behavioral therapy for nightmares; CBT-N) among firefighters. The main questions it aims to answer are:

  • Is the behavioral intervention feasible, acceptable, and effective in reducing symptoms of posttraumatic stress, insomnia, and nightmares?
  • What is the efficacy of efficient treatment vs. delayed treatment (2-4 week waitlist) in reducing symptoms of posttraumatic stress, insomnia, and nightmares?

We will beta test the intervention in 1-2 groups of 3-5 firefighters. Then we will randomize 50 participants to immediate or delayed (2-4 week waitlist) treatment. Consented participants will:

  • Complete self-report and interview measures assessing posttraumatic stress disorder, insomnia (PTSD), and nightmares
  • Attend an individual treatment orientation session
  • Attend a 4-day (~3 hours per day over 4 consecutive days) group treatment that integrates WET, CBT-I, and CBT-N
  • Attend an individual booster session held approximately one week later
  • Complete self-report measures before, during, and after treatment, and at a 3-month follow up assessment and a clinical interview before and after treatment to assess program efficacy.

Enrollment

50 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18-65 years old
  • Firefighter
  • Able to speak and read English
  • Clinically significant posttraumatic stress symptoms: CAPS-5 total score ≥ 25; ≥ 1 intrusion symptom; ≥ 1 avoidance symptom
  • Clinically significant symptoms of insomnia: SCISD insomnia criteria are met; ISI ≥ 15
  • Clinically significant symptoms of nightmare disorder: SCISD nightmare disorder criteria are met, nightmares ≥ 1 monthly.

Exclusion criteria

  • Current suicide or homicide risk meriting crisis intervention
  • Inability to speak and read English
  • Inability to comprehend the baseline screening questionnaires
  • Unwilling to remain abstinent from alcohol during treatment
  • Serious mental health diagnosis such as bipolar disorder or psychosis.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

50 participants in 2 patient groups

Immediate Intervention
Experimental group
Description:
Will begin treatment within 2 weeks of randomization.
Treatment:
Behavioral: Cognitive Behavioral Therapy for Nightmares (CBTn)
Behavioral: Cognitive Behavioral Therapy for Insomnia (CBTi)
Behavioral: Written Exposure Therapy (WET)
Delayed Intervention
Active Comparator group
Description:
Will be scheduled to begin treatment within 4-6 weeks of randomization.
Treatment:
Behavioral: Waitlist

Trial contacts and locations

1

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Central trial contact

Sara A Jahnke, PhD; Carrie Sutherland, MS

Data sourced from clinicaltrials.gov

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