Trials / Completed
CompletedNCT01622855
Acute Intervention to Reduce Distress Following Sexual Assault
Prevention of Post-Rape Psychopathology and Drug Abuse
- Status
- Completed
- Phase
- Phase 1 / Phase 2
- Study type
- Interventional
- Enrollment
- 442 (actual)
- Sponsor
- Medical University of South Carolina · Academic / Other
- Sex
- Female
- Age
- 14 Years – 90 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study was to evaluate whether a brief intervention in video format delivered in the post assault medical exam setting and including education about assault reactions and instruction in and modeling of successful coping strategies would reduce post assault drug use or abuse and PTSD symptoms as compared to standard care.
Detailed description
The intervention being evaluated was shown at the time of the post assault medical exam and includes two main components: preparation for the medical exam; and information about and modelling of coping strategies that may help women cope in the aftermath of assault. The intervention content is delivered via video. Intervention and standard care groups were compared with regard to measures of substance use and abuse and symptoms of PTSD and other potentially comorbid problems including symptoms of depression or other anxiety.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| BEHAVIORAL | PPRS | Video including psycho-education and modeling of adaptive behavioral coping strategies for use post-assault. |
Timeline
- Start date
- 1997-03-01
- Primary completion
- 2005-09-01
- Completion
- 2005-09-01
- First posted
- 2012-06-19
- Last updated
- 2015-04-22
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01622855. Inclusion in this directory is not an endorsement.