PTSD Clinical Trial
Official title:
Neurobiology of Sleep and Sleep Treatment Response in Returning Veterans
The overarching objectives of this study are: 1) To investigate the neurobiology of
posttraumatic stress disorder (PTSD) during REM and NREM sleep relative to wakefulness; 2)
To identify the neurobiological underpinnings of sleep treatment response to prazosin or
placebo during wakefulness, REM sleep, and NREM sleep in OIF/OEF veterans with PTSD; and 3)
To explore pre-treatment brain activity patterns during wakefulness, REM sleep, and NREM
sleep that predict sleep treatment response. We will also explore the stability of the PET
signal by comparing pre- and post-placebo changes in brain glucose metabolism in
non-responders. For non-PTSD veterans, the stability of the PET signal will be evaluated in
a subsample of 6 veterans without PTSD who will repeat the PET imaging procedures 8 weeks
after the initial PET series.
The overarching hypothesis is that PTSD is characterized by neurobiological alterations in
the amygdala, mPFC, and brain centers involved in the regulation of NREM and REM sleep, and
that these neurobiological changes are normalized with effective sleep treatment.
PTSD affects both daytime functioning and sleep. Complaints of poor sleep, objective disruption of sleep, and heightened sympathovagal tone during sleep occurring early after trauma exposure increase the risk of developing PTSD up to one year later. (1-4). Insomnia is one the most common reasons for referral to mental health services in active duty personnel (5). In military personnel returning from Iraq and Afghanistan, more than 70 percent of those with PTSD report sleep problems and fatigue, whereas more than 25% percent of those without PTSD endorse these symptoms (6). Other disruptive nocturnal behaviors and sleep disorders including sleep terrors, nocturnal anxiety attacks, simple and complex motor behaviors and vocalizations, acting out dreams, sleep apnea, and periodic leg movement disorders are also frequently reported by PTSD patients (7-12). In PTSD, sleep disturbances independently contribute to poor clinical outcomes such as increased severity of daytime PTSD symptoms (8), depression (13), suicidality (13), general psychiatric distress (14), poorer quality of life and functioning (14), poorer perceived physical health (14), and increased substance use (15;16). ;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
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