Relationship Between the Biological and Psychological Correlates of PTSD
Completed · Phase 2
Conditions studied: Post-Traumatic Stress Disorder
In brief
This study will determine the effectiveness of immediate treatment with prolonged exposure therapy (PE) versus delaying treatment with PE in altering neuroendocrine-related symptoms of post-traumatic stress disorder in women.
Key facts
- Study ID
- NCT00183300
- Run by
- University of Pennsylvania
- People needed
- 120
- Starts
- 2001-09-01
- Expected to finish
- 2007-07-01
- Last updated by the study team
- 2015-10-06
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Chronic post-traumatic stress disorder
- Minimum of 3 months passed since traumatic event happened
- Agree to use an effective form of contraception throughout the study
You may not qualify if…
- History of schizophrenia, bipolar disorder, or cognitive dysfunction due to a general medical condition
- History of alcohol or other drug abuse or dependence within 3 months of study enrollment
- Mental retardation or other pervasive developmental disorder
- Unwillingness or inability to discontinue current psychotherapy treatment (stable psychiatric medication therapy taken during the study is not criteria for exclusion)
- Significant risk of violence or history of serious violent behavior within one year of study enrollment
- Medically unstable condition
- Continuing intimate relationship with the perpetrator when the trauma involves assault
- At risk for suicide risk
- Currently pregnant
Where it is running
- Center for the Treatment and Study of Anxiety, University of Pennsylvania — Philadelphia, Pennsylvania, United States
Full record on ClinicalTrials.gov
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