Prevention of Post Sexual Assault Stress

Status Completed

Clinical Trial Summary

The purpose of this study is to evaluate whether a brief intervention in video format, that includes education about reactions to assault and modeling of adaptive coping strategies, designed to reduce post assault drug use or abuse and PTSD and shown to recent victims of sexual assault at the time of receipt of post assault medical care is associated with better post-assault outcomes as compared to a comparable length video that includes pleasant imagery and relaxation instruction or standard care.

Clinical Trial Description

Post assault outcomes include coping behaviors and PTSD symptoms. ;

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Prevention

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01430624
Study type	Interventional
Source	Medical University of South Carolina
Contact
Status	Completed
Phase	Phase 1/Phase 2
Start date	May 2009
Completion date	December 2013

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