Clinical Trials Directory

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

TypeNameDescription
BEHAVIORALPPRSVideo 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.