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UnknownNCT01090518

Cortisol Augmentation of a Psychological Treatment in Warfighters With Post Traumatic Stress Disorder (PTSD)

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
50 (estimated)
Sponsor
Bronx VA Medical Center · Federal
Sex
All
Age
18 Years – 89 Years
Healthy volunteers
Not accepted

Summary

This study seeks to examine the efficacy of hydrocortisone administration in the augmentation of the therapeutic effects of Prolonged Exposure (PE) therapy, an empirically tested treatment shown to be effective in the the treatment of posttraumatic stress disorder (PTSD). The augmentation builds on both the translation of neuroscience findings demonstrating the effects of glucocorticoids (GCs) on learning, and on empirical clinical findings from other investigators demonstrating beneficial effects of GCs in reducing traumatic memories in trauma-exposed persons.

Conditions

Interventions

TypeNameDescription
BEHAVIORALProlonged Exposure therapy10 weekly sessions
DRUGHydrocortisone30mg 20 minutes prior to each PE session including imaginal exposure (8 total)
BEHAVIORALProlonged Exposure therapy10 weekly sessions

Timeline

Start date
2010-02-01
Primary completion
2013-11-01
First posted
2010-03-22
Last updated
2013-02-05

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01090518. Inclusion in this directory is not an endorsement.

Cortisol Augmentation of a Psychological Treatment in Warfighters With Post Traumatic Stress Disorder (PTSD) (NCT01090518) · Clinical Trials Directory