Project Remission: Maximizing Outcomes With Intensive Treatments for Combat-Related PTSD
Posttraumatic Stress Disorder (PTSD)
About this trial
This is an interventional treatment trial for Posttraumatic Stress Disorder (PTSD) focused on measuring Posttraumatic Stress Disorder, PTSD, Post-Traumatic Stress, Trauma and Stressor Related Disorders, Trauma, Combat, Military, Veterans, Prolonged Exposure, Exposure Therapy, Behavior Therapy, Psychological Treatment, Psychotherapy
Eligibility Criteria
Inclusion Criteria:
- Active duty military service member or veteran (age 18- 65 years) who deployed in support of combat operations post-9/11 seeking behavioral health treatment for PTSD.
- PTSD diagnosis as assessed by Clinician-Administered Posttraumatic Stress Scale (CAPS-5).
- Able to speak and read English (due to standardization of outcome measures)
Exclusion Criteria:
- Current manic episode or a psychotic symptoms requiring immediate stabilization or hospitalization (as determined by the bipolar and psychosis modules of the MINI).
- Current and severe alcohol use warranting immediate intervention based on clinical judgment.
- Evidence of a moderate or severe traumatic brain injury (as determined by the inability to comprehend the baseline screening questionnaires).
- Current suicidal ideation severe enough to warrant immediate attention (as determined by the Depressive Symptoms Index-Suicidality Subscale and corroborated by a clinical risk assessment by a credentialed provider)
- Other psychiatric disorders severe enough to warrant designation as the primary disorder as determined by clinician judgment.
Sites / Locations
- Carl R. Darnall Army Medical Center
- South Texas Veterans Health Care System
- Brooke Army Medical Center
- Central Texas Veterans Health Care System
Arms of the Study
Arm 1
Arm 2
Active Comparator
Experimental
Massed Prolonged Exposure
Intensive Outpatient Prolonged Exposure
Participants will complete fifteen weekday 90-minute Prolonged Exposure therapy sessions over three consecutive weeks. If necessary, the treatment window may be extended for another week.
The IOP-PE will include the same primary treatment components as the Massed-PE protocol (fifteen weekday 90-minute PE sessions delivered five days a week over a three-week period) plus eight augmentations designed to maximize treatment outcomes. Similar to the Mass-PE, participants will have three consecutive weeks to complete treatment; however, the treatment window may be extended another week if necessary.