Prevention of Post Sexual Assault Stress
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.
Posttraumatic Stress Disorder
|Study Design:||Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Outcomes Assessor)
Primary Purpose: Prevention
|Official Title:||Prevention of Postrape Drug Abuse: Replication Study|
- Frequency of specific drug use [ Time Frame: 14 days ] [ Designated as safety issue: No ]Number of days use of specific drugs in preceding 14 days at 6 week, 3 and 6 month follow-ups
- DAST-10 [ Time Frame: Baseline and 6 months ] [ Designated as safety issue: No ]Past 12 months assessed at baseline, post assault at 6 months
- AUDIT [ Time Frame: Baseline, 6 months ] [ Designated as safety issue: No ]Past 12 months assessed at baseline, post assault at 6 months
- PSS-SR [ Time Frame: 2 weeks ] [ Designated as safety issue: No ]Measure of PTSD symptoms.
|Study Start Date:||May 2009|
|Study Completion Date:||December 2013|
|Primary Completion Date:||December 2013 (Final data collection date for primary outcome measure)|
Experimental: PPRS video
Prevention of post sexual assault stress
Video including information psychoeducation and modeling of adaptive behavioral coping strategies for use post-assault. Shown at time of post assault medical exam.
Active Comparator: PIRI video
Pleasant imagery and relaxation instruction
Video containing pleasant imagery and relaxation instruction information. Shown at time of post assault medical exam.
No Intervention: Standard care
Treatment as usual
Post assault outcomes include coping behaviors and PTSD symptoms.
Please refer to this study by its ClinicalTrials.gov identifier: NCT01430624
|United States, Minnesota|
|Hennepin County Medical Center|
|Minneapolis, Minnesota, United States, 55404|
|North Memorial Medical Center|
|Minneapolis, Minnesota, United States, 55422|
|Principal Investigator:||Heidi Resnick, Ph.D.||Medical University of South Carolina|