Trials / Unknown
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
| Type | Name | Description |
|---|---|---|
| BEHAVIORAL | Prolonged Exposure therapy | 10 weekly sessions |
| DRUG | Hydrocortisone | 30mg 20 minutes prior to each PE session including imaginal exposure (8 total) |
| BEHAVIORAL | Prolonged Exposure therapy | 10 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.