Awardee OrganizationVA NORTH TEXAS HEALTH CARE SYSTEM
Description
Abstract Text
Abstract
There are very few systematic studies on humans that focus on changing the underlying traumatic memory once
PTSD has been established. The proposed project is a translational study based on our work with animal models
of PTSD in which coricosterone augmented extinction of contextual fear memories. The study design is a
double-blind randomized controlled clinical trial involving eighty-eight OEF/OIF veterans with combat-related
PTSD. We plan to pair multiple fear memory reactivations, using a scripted imagery technique, with an oral
glucocorticoid or placebo. Participants will be followed at 1, 3, and 6 months post intervention to measure the
longevity of the expected effect. Outcome measures will include PTSD symptom severity, depression
symptoms severity, and physiological measures.
Specific Aims/Hypothesis:
Aim 1: Examine the effects of glucocorticoid administration following traumatic memory reactivation on
psychiatric symptoms in veterans with combat-related PTSD.
Specific hypotheses to be tested:
(A) Subjects who receive an exogenous glucocorticoid after traumatic memory reactivation will demonstrate
fewer PTSD and depression symptoms one week later, compared to those who receive a placebo after
traumatic memory reactivation.
(B) The glucocorticoid reduction effects will be cumulative; that is, reduction will persist, and further post-
reactivation glucocorticoid administration will further reduce symptoms.
(C) Decreases in PTSD and depression symptoms will persist at 1, 3, and 6 months for subjects receiving an
exogenous glucocorticoid compared to those subjects receiving placebo.
Aim 2: Examine the effects of glucocorticoid administration following traumatic memory reactivation on
physiological responses to veteran's personal combat memories.
(D) Subjects who receive an exogenous glucocorticoid after traumatic memory reactivation will demonstrate
decreased physiological responses one week later, compared to those who receive a placebo after
traumatic memory reactivation.
(E) As with the psychological measures, suppression of the physiological measures will demonstrate both
persistence over time and accumulation with subsequent post-reactivation glucocorticoid administration.
Public Health Relevance Statement
Project Narrative
Prevalence rates of combat-related post-traumatic stress disorder (PTSD) are increasing
because of Operation Enduring Freedom/Operation Iraqi Freedom (OEF/OIF)
deployments, with the estimated risk for PTSD from OEF/OIF service ranging from 11%
to 18%. PTSD is characterized by intrusive memories in the form of unwanted images,
nightmares, and flashbacks as the result of being exposed to a traumatic event. These
memories are associated with intense distressand involve excessive physiological and
psychological responses to trauma related stimuli. Current research efforts are focused on
exploring the underlying neurochemical changes associated with PTSD in an effort to
prevent or treat associated traumatic memories. To date, there have been very few
systematic studies on humans that focus on changing the underlying traumatic memories
once PTSD has been established. Memory can be changed in various ways including
interference with reconsolidation of an established fear memory or by extinction, in
which new memories associated with the trauma are formed. A traditional behavior
therapy called exposure therapy uses the same process of extinction that we are using in
the proposed study. Although effective, this therapy is not widely used because of
barriers perceived by the providers of therapy as well as the recipients. The proposed
study is a novel approach to treatment for established PTSD, applying an animal model
of fear memory extinction to humans, to augment the extinction of underlying traumatic
memories related to combat by pairing reactivation of a traumatic memory with a
glucocorticoid. We will measure veterans' responses to scripts of their own combat
traumas by looking at their physiological responses as well as self-reported psychiatric
symptoms of PTSD and depression as well as clinician rated assessments of PTSD. The
results of this study may offer a unique, inexpensive, and rapid method to treat PTSD, as
well as lay the groundwork for the development of other pharmacotherapeutic agents that
specifically target the extinction of combat-related fear memories. Although we are not
developing a new type of exposure therapy, because we are using the same extinction
principles as traditional exposure therapy uses, the information provided by this study
will lay the groundwork for future studies combining pharmacotherapy and behavior
therapy. The information gained from this study will be applicable not only to veterans
who have combat-related PTSD, but to any individual with suffering intrusive memories
from any type of trauma.
No Sub Projects information available for 5I01RX000178-02
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