Exposure Therapy for Active Duty Soldiers With Post Traumatic Stress Disorder
VRPE
Comparing Virtual Reality Exposure Therapy to Prolonged Exposure in the Treatment of Soldiers With PTSD
2 other identifiers
interventional
162
1 country
1
Brief Summary
This study is evaluating the efficacy of virtual realty exposure therapy (VRET)by comparing it to prolonged exposure therapy (PE) and a waitlist (WL) group for the treatment of post traumatic stress disorder (PTSD) in active duty (AD) Soldiers with combat-related trauma. The investigators will test the general hypotheses that 10 sessions of VRET or PE will successfully treat PTSD, therapeutically affect levels of physiological arousal, and significantly reduce perceptions of stigma toward seeking behavioral health services.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Mar 2009
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 1, 2009
CompletedFirst Submitted
Initial submission to the registry
August 30, 2010
CompletedFirst Posted
Study publicly available on registry
September 2, 2010
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2013
CompletedStudy Completion
Last participant's last visit for all outcomes
November 1, 2014
CompletedApril 14, 2015
April 1, 2015
4.7 years
August 30, 2010
April 13, 2015
Conditions
Keywords
Outcome Measures
Primary Outcomes (5)
Clinician-Administered PTSD Scale (CAPS)
The CAPS is a structured interview that assesses all DSM-IV PTSD criteria in terms of frequency and intensity. Scores are computed for Intrusion, Avoidance and Hyperarousal symptom clusters, as well as a Total score.
Screening Visit ( Day 1)
Clinician-Administered PTSD Scale (CAPS)
The CAPS is a structured interview that assesses all DSM-IV PTSD criteria in terms of frequency and intensity. Scores are computed for Intrusion, Avoidance and Hyperarousal symptom clusters, as well as a Total score.
2.5 weeks (or after treatment session 5)
Clinician-Administered PTSD Scale (CAPS)
The CAPS is a structured interview that assesses all DSM-IV PTSD criteria in terms of frequency and intensity. Scores are computed for Intrusion, Avoidance and Hyperarousal symptom clusters, as well as a Total score.
5 weeks (or after treatment session 10)
Clinician-Administered PTSD Scale (CAPS)
The CAPS is a structured interview that assesses all DSM-IV PTSD criteria in terms of frequency and intensity. Scores are computed for Intrusion, Avoidance and Hyperarousal symptom clusters, as well as a Total score.
12 Week follow-up
Clinician-Administered PTSD Scale (CAPS)
The CAPS is a structured interview that assesses all DSM-IV PTSD criteria in terms of frequency and intensity. Scores are computed for Intrusion, Avoidance and Hyperarousal symptom clusters, as well as a Total score.
26 Week follow-up
Secondary Outcomes (70)
PTSD Checklist (PCL-C)
Screening Visit (Day 1)
Primary Care PTSD Screen (PC-PTSD)
Screening Visit(Day 1)
Beck Depression Inventory-II (BDI-II)
Screening Visit(Day 1)
Inventory of Attitudes Toward Seeking Mental Health Services (IASMHS)
Screening Visit(Day 1)
Perceived Stigma Measure (PSS)
Screening Visit(Day 1)
- +65 more secondary outcomes
Study Arms (3)
Prolonged Exposure Therapy (PE)
ACTIVE COMPARATORThe PE protocol is based on manualized procedures, which are derived from the theory that effective treatment for PTSD requires that the underlying pathological fear structure be activated and paired with new information that is incompatible with the fear structure. PE involves imaginal exposure and in vivo exposure as the two primary strategies to elicit repeated confrontation of feared but objectively safe thoughts, feelings, situations and events.
Virtual Reality Exposure Therapy (VRET)
EXPERIMENTALThe VRET protocol follows the same procedures as the PE protocol with the primary exception being that all instances of imaginal exposure will be augmented by immersion into Virtual Iraq environments, thus creating a situation known as immersive exposure.
Waitlist
PLACEBO COMPARATORThe waitlist (WL) participants will be asked to refrain from psychotherapy during the 5 weeks of study participation.
Interventions
Prolonged exposure therapy will consist of 10 treatment sessions lasting 90 - 120 minutes each, with additional between-session homework assignments.
Virtual Reality Exposure Therapy will consist of 10 treatment sessions lasting 90 -120 minutes with additional between-session homework assignments.
This group will refrain from psychotherapy until after the completion of the 5 weeks of study participation
Eligibility Criteria
You may qualify if:
- PTSD diagnosis as assessed by CAPS
- history of deployment in support of OIF/OEF
- non sexually based deployment related trauma
- three or more months since index trauma
- stable on psychotropic medications for 30 days
You may not qualify if:
- index trauma in the last three months
- history of schizophrenia, other psychotic or bipolar disorder
- history of organic brain disorder
- suicidal risk or intent or self-mutilating behavior requiring hospitalization in the last 6 months
- ongoing threatening situation
- current drug or alcohol dependence
- history of seizures
- prior history of PE for PTSD
- other current psychotherapy
- physical condition that interferes with proper use of Virtual Reality head mounted display
- history of loss of consciousness since entering active duty service greater than 15 minutes
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
National Center for Telehealth and Technology
Tacoma, Washington, 98431, United States
Related Publications (84)
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PMID: 31880749DERIVED
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Gregory A Gahm, PhD
DCoE - National Center for Telehealth and Technology
- PRINCIPAL INVESTIGATOR
Greg Reger, PhD
DCoE - National Center for Telehealth and Technology
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- FED
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 30, 2010
First Posted
September 2, 2010
Study Start
March 1, 2009
Primary Completion
November 1, 2013
Study Completion
November 1, 2014
Last Updated
April 14, 2015
Record last verified: 2015-04