Integrated CBT-I and PE on Sleep and PTSD Outcomes (Impact Study)
Primary Purpose
Posttraumatic Stress Disorders, Chronic Insomnia
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
CBTI-PE
Hygiene-PE
Sponsored by
About this trial
This is an interventional treatment trial for Posttraumatic Stress Disorders focused on measuring PTSD, insomnia, CBT-I, Prolonged Exposure, Veteran
Eligibility Criteria
Inclusion Criteria:
- Over the age of 19 years old
- Diagnosis of PTSD
- Meet diagnostic criteria for insomnia
- Enrolled at the VA San Diego Healthcare System (VASDHS) and living within 50 miles of the respective facility
- English literacy
Exclusion Criteria:
- Unmanaged psychosis or manic episodes in past year
- Substance/alcohol use disorder in past 6 months
Diagnosed (previously or by the investigators' study screen) and untreated sleep disorder other than insomnia
- Sleep disorders diagnosed, but stably treated, such as obstructive sleep apnea treated with continuous positive airway pressure (CPAP), will be allowed)
Participation in concurrent psychotherapies targeting PTSD
- Veteran can be reassessed after their PTSD treatment concludes
- Veterans who are engaged in treatment for non-PTSD symptoms (e.g., 12-step programs) will be eligible
- Severe medical or psychiatric illness that would make it difficult to regularly attend psychotherapy sessions or participate fully in the study
- History of moderate to severe cognitive impairment
Sites / Locations
- VA San Diego Healthcare System, San Diego, CA
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
CBTI-PE
Hygiene-PE
Arm Description
Integrates the core components of CBT-I and PE in 14 90-minute weekly sessions.
Uses non-active sleep hygiene to account for the dose response of experimental condition before starting PE. Uses 14 90-minute weekly sessions.
Outcomes
Primary Outcome Measures
Change in PTSD Symptoms
Change in PTSD Symptoms will be assessed using the Clinician-Administered PTSD Scale DSM 5 (CAPS-5)
Secondary Outcome Measures
Change in Sleep Efficiency
Change in sleep efficiency, calculated as time spent sleeping divided by time spent in bed. This data is acquired from daily sleep logs filled out by patient.
Change in Quality of Life
Change in Quality of life will be assessed using the World Health Organization Quality of Life-BREF (WHOQOL-BREF) questionnaire.
Full Information
NCT ID
NCT02774642
First Posted
May 10, 2016
Last Updated
October 19, 2022
Sponsor
VA Office of Research and Development
1. Study Identification
Unique Protocol Identification Number
NCT02774642
Brief Title
Integrated CBT-I and PE on Sleep and PTSD Outcomes (Impact Study)
Official Title
The Impact of Integrated CBT-I and PE on Sleep and PTSD Outcomes
Study Type
Interventional
2. Study Status
Record Verification Date
October 2022
Overall Recruitment Status
Completed
Study Start Date
October 1, 2016 (Actual)
Primary Completion Date
September 30, 2022 (Actual)
Study Completion Date
September 30, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
VA Office of Research and Development
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study aims to examine whether integrating insomnia and PTSD treatment will enhance sleep, PTSD, and quality of life outcomes. This is a randomized control trial comparing integrated evidence based CBT-I into PE (CBTI-PE) versus to a non-active sleep component plus PE (hygiene-PE) to optimize PTSD, sleep, and quality of life outcomes in 90 Veterans. Such benefits would further the VA's commitment to improving the mental health, recovery, and community reintegration of Veterans detailed in the 2014-2020 VHA Strategic Plan. Findings from the proposed study offer a unique opportunity to determine the malleability of mechanisms (e.g., Total sleep time, Sleep efficiency) that can improve recovery outcomes among this vulnerable population and to inform future treatment development and research. Improved PTSD, insomnia, and quality of life outcomes can decrease risk of chronic impairment and ultimately help affected Veterans live richer, more productive lives.
Detailed Description
The lifetime prevalence of posttraumatic stress disorder (PTSD) is approximately 30% among Vietnam Veterans and 11-17% among Iraq and Afghanistan Veterans. PTSD is associated with enormous health care costs, increased suicidality, depression, poorer quality of life and functioning, physical health, and increased substance use. Prolonged exposure (PE) is an efficacious treatment for Veterans with PTSD that decreases avoidance of feared, but safe, cues. Despite PE being one of the best available treatments for PTSD, 25 to 45% of PTSD patients still meet diagnostic criteria following treatment. High rates of comorbid disorders, such as insomnia, may interfere with the efficacy of PE and limit long-term rehabilitation outcomes.
Among Veterans with PTSD, sleep disturbances are nearly universal with 70 - 87% reporting comorbid insomnia. Untreated insomnia can persist for years, is independently associated with impaired health-related quality of life, does not resolve following PTSD treatment, and can exacerbate daytime PTSD symptoms.
Importantly, insomnia may interfere with the mechanisms of PE through safety learning, habituation to feared stimuli, emotional coping, emotional processing, and cognitive abilities necessary for successful treatment.
Despite this, insomnia is not a primary intervention for Veterans with PTSD. Given these factors, it is critical to evaluate whether treating insomnia prior to PTSD will improve PTSD symptoms and quality of life outcomes. Cognitive behavioral treatment for insomnia (CBT-I) is the first line treatment of chronic and severe insomnia, which produces lasting improvements in sleep. By using CBT-I prior to, and integrated with, PE offers several novel advantages that will: 1) increase client-centered treatment by addressing the number one subjective complaint among Veterans with PTSD; 2) enhance PTSD outcomes and non-response rates by addressing insomnia-related factors that interfere with PTSD treatment; 3) act as a stepping stone and help to engage patients who are not initially willing to engage in trauma-focused PE; 4) increase rehabilitation outcomes by addressing the two leading disorders that independently affect quality of life for Veterans; 5) allow patients to address both symptoms of insomnia and PTSD within a shortened timeframe; 6) increase continuity by allowing patients to work with a single provider; and 7) decrease the risk of attrition between referral clinics and waitlists. To date, no studies have capitalized on available evidence-based CBT-I prior to PE to improve insomnia, PTSD, and quality of life outcomes.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Posttraumatic Stress Disorders, Chronic Insomnia
Keywords
PTSD, insomnia, CBT-I, Prolonged Exposure, Veteran
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
92 (Actual)
8. Arms, Groups, and Interventions
Arm Title
CBTI-PE
Arm Type
Experimental
Arm Description
Integrates the core components of CBT-I and PE in 14 90-minute weekly sessions.
Arm Title
Hygiene-PE
Arm Type
Active Comparator
Arm Description
Uses non-active sleep hygiene to account for the dose response of experimental condition before starting PE. Uses 14 90-minute weekly sessions.
Intervention Type
Behavioral
Intervention Name(s)
CBTI-PE
Intervention Description
Integrates CBT-I and PE with the goal of enhancing both insomnia and PTSD outcomes. Integrated treatment will be delivered in 14 90-minute weekly sessions. CBTI-PE starts with VA rollout CBT-I for the first 3 weeks with a focus on the effects of PTSD on insomnia. PE protocol (psychoeducation) begins on week 4 of treatment and both treatments overlap till week 6 when CBT-I ends and the active treatment of PE begins (i.e., imaginal and in-vivo exposures). However, CBT-I sleep diary review and sleep time adjustment will continue till the end of treatment to increase adherence
Intervention Type
Behavioral
Intervention Name(s)
Hygiene-PE
Intervention Description
The investigators have included a non-active sleep control arm (3 Sessions)to allow for the dose response of 14 90 minute sessions. The non-active sleep control condition used in this study is a manualized protocol developed to exclude the active components of standard CBT-I treatment. Hygiene includes presentation of sleep hygiene education and reviewing daily stressors that may impact sleep before starting PE on week 4.
Primary Outcome Measure Information:
Title
Change in PTSD Symptoms
Description
Change in PTSD Symptoms will be assessed using the Clinician-Administered PTSD Scale DSM 5 (CAPS-5)
Time Frame
Baseline, Post Treatment (14-weeks), Follow-up (26-weeks)
Secondary Outcome Measure Information:
Title
Change in Sleep Efficiency
Description
Change in sleep efficiency, calculated as time spent sleeping divided by time spent in bed. This data is acquired from daily sleep logs filled out by patient.
Time Frame
Baseline, Post Treatment (14-weeks), Follow-up (26-weeks)
Title
Change in Quality of Life
Description
Change in Quality of life will be assessed using the World Health Organization Quality of Life-BREF (WHOQOL-BREF) questionnaire.
Time Frame
Baseline, Post Treatment (14-weeks), Follow-up (26-weeks)
Other Pre-specified Outcome Measures:
Title
The Client Satisfaction Questionnaire (CSQ)
Description
CSQ assesses client satisfaction for therapy session
Time Frame
up to 26 weeks
Title
Pain Disability Questionnaire (PDQ)
Description
PDQ assesses functional impairment due to pain
Time Frame
up to 26 weeks
Title
Nox T3 recorders - Obstructive Sleep Apnea (OSA)
Description
The Nox T3 recorders are a portable sleep monitoring system that can accurately diagnose OSA.
Time Frame
Pre-Treatment
Title
Medications Use Interview:
Description
Assesses medication use
Time Frame
Pre-treatment
10. Eligibility
Sex
All
Minimum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Over the age of 19 years old
Diagnosis of PTSD
Meet diagnostic criteria for insomnia
Enrolled at the VA San Diego Healthcare System (VASDHS) and living within 50 miles of the respective facility
English literacy
Exclusion Criteria:
Unmanaged psychosis or manic episodes in past year
Substance/alcohol use disorder in past 6 months
Diagnosed (previously or by the investigators' study screen) and untreated sleep disorder other than insomnia
Sleep disorders diagnosed, but stably treated, such as obstructive sleep apnea treated with continuous positive airway pressure (CPAP), will be allowed)
Participation in concurrent psychotherapies targeting PTSD
Veteran can be reassessed after their PTSD treatment concludes
Veterans who are engaged in treatment for non-PTSD symptoms (e.g., 12-step programs) will be eligible
Severe medical or psychiatric illness that would make it difficult to regularly attend psychotherapy sessions or participate fully in the study
History of moderate to severe cognitive impairment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Peter Colvonen, PhD
Organizational Affiliation
VA San Diego Healthcare System, San Diego, CA
Official's Role
Principal Investigator
Facility Information:
Facility Name
VA San Diego Healthcare System, San Diego, CA
City
San Diego
State/Province
California
ZIP/Postal Code
92161
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
34216197
Citation
Lyons R, Barbir LA, Owens R, Colvonen PJ. STOP-BANG screener vs objective obstructive sleep apnea testing among younger veterans with PTSD and insomnia: STOP-BANG does not sufficiently detect risk. J Clin Sleep Med. 2022 Jan 1;18(1):67-73. doi: 10.5664/jcsm.9498.
Results Reference
derived
Learn more about this trial
Integrated CBT-I and PE on Sleep and PTSD Outcomes (Impact Study)
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