RECRUITING

Treatments in Women Veterans With Insomnia and PTSD

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This pilot trial will compare trauma-informed Cognitive Behavioral Therapy for Insomnia (CBT-I) to a psychoeducational intervention in women Veterans with comorbid insomnia and posttraumatic stress disorder (PTSD). The CBT-I intervention includes trauma-informed adaptations to an insomnia treatment and the psychoeducational intervention is modeled after usual care in a VA Women's Mental Health Clinic. The study objectives are to: 1) Iteratively refine the structure and materials of trauma-informed CBT-I in preparation for a pilot trial, 2) Pilot test the effects of trauma-informed CBT-I on PTSD treatment readiness and engagement in a sample of women Veterans, and 3) Examine potential mechanisms underlying variations in PTSD treatment readiness and engagement over time among women Veterans. Women Veterans with insomnia and comorbid PTSD who receive care at Sepulveda and West Los Angeles facilities will be recruited for the study. Those who pass an initial eligibility screen will be enrolled and written informed consent will be obtained. A baseline assessment will be completed that includes measures of PTSD treatment readiness, perceived barriers to PTSD treatment, and sleep and mental health symptoms. Then Veterans who meet all eligibility criteria will be randomly assigned to trauma-informed CBT-I (n=25) or the psychoeducational intervention (n=25). Both treatments will be provided in 5 one-on-one sessions by a trained instructor who is supervised by a behavioral sleep medicine specialist. All randomized participants (n=50) will have 2 follow-up assessments (post-treatment and 3-months). The follow-up assessments will collect information on PTSD treatment readiness, perceived barriers to PTSD treatment, and sleep and mental health symptoms. Chart reviews will be conducted 6-months post-treatment to assess number of PTSD treatment appointments attended (treatment engagement measure). Qualitative interviews will be conducted to identify mechanisms underlying PTSD treatment engagement.

Official Title

Increasing PTSD Treatment Engagement in Women Veterans: Role of CBT for Insomnia (CDA 20-227)

Quick Facts

Study Start:2023-06-01
Study Completion:2028-12-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05683132

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Community-dwelling women Veterans aged 18 years and older
  2. * Received care from VAGLAHS
  3. * Have symptoms of PTSD
  4. * Have symptoms of insomnia
  1. * Reported health or emotional problems, or use of drugs or alcohol that would make it difficult for them to participate in this study
  2. * Too ill to engage in the study procedures
  3. * Unable to self-consent to participate
  4. * Previously engaged in Cognitive Behavioral Therapy for Insomnia (CBT-I) treatment
  5. * Previously engaged in PTSD psychoeducational group offered in VAGLAHS Women's Health Clinic
  6. * Previously completed \>3 sessions of PTSD treatment (Cognitive Processing Therapy and/or Prolonged Exposure)
  7. * Pregnant or pregnant within 6 months of study
  8. * Untreated moderate to severe obstructive sleep apnea diagnosis as evidenced by Apnea Hypopnea Index (AHI) in chart and/or screens that indicate high risk
  9. * Unstable housing
  10. * Inability to read, write, and communicate in English
  11. * Unstable medical or psychiatric disorders (which is a contraindication for behavioral treatment of insomnia)
  12. * Remission of PTSD or insomnia symptoms

Contacts and Locations

Study Contact

Michael K Ong, MD PhD
CONTACT
(310) 478-3711
Michael.Ong2@va.gov
Scott E Krahl, PhD MA BA
CONTACT
(818) 895-5861
scott.krahl@va.gov

Principal Investigator

Gwendolyn C Carlson, PhD
PRINCIPAL_INVESTIGATOR
VA Greater Los Angeles Healthcare System, West Los Angeles, CA

Study Locations (Sites)

VA Greater Los Angeles Healthcare System, West Los Angeles, CA
West Los Angeles, California, 90073-1003
United States

Collaborators and Investigators

Sponsor: VA Office of Research and Development

  • Gwendolyn C Carlson, PhD, PRINCIPAL_INVESTIGATOR, VA Greater Los Angeles Healthcare System, West Los Angeles, CA

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-06-01
Study Completion Date2028-12-31

Study Record Updates

Study Start Date2023-06-01
Study Completion Date2028-12-31

Terms related to this study

Keywords Provided by Researchers

  • Insomnia Disorder
  • Posttraumatic Stress Disorder
  • Women's Health

Additional Relevant MeSH Terms

  • Insomnia
  • PTSD
  • Women Veterans