CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 245 enrolled
Drug / intervention
PPRS +1 morebehavioral
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01430624
NCT01430624Phase 2Completed
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Prevention of Postrape Drug Abuse: Replication Study

Medical University of South Carolina·interventional·Posted Sep 8, 2011·Updated Apr 13, 2016

In Brief

A Phase 2 clinical trial evaluating PPRS and PIRI for Drug Use and 2 related conditions. Completed, enrolled 245 participants across 2 sites.

Detailed 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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsDrug Use, Drug Abuse, Posttraumatic Stress Disorder
CountriesUnited States
CollaboratorsNational Institute on Drug Abuse (NIDA)

Timeline

Phase 2CompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
First PostedSep 8, 2011
Enrollment StartMay 1, 2009
Primary CompletionDec 1, 2013
TodayJul 2, 2026
Enrollment to primary: 4.6 yearsPosted 14.8 years ago

Interventions

PPRSbehavioral

Video including information psychoeducation and modeling of adaptive behavioral coping strategies for use post-assault. Shown at time of post assault medical exam.

PIRIbehavioral

Video containing pleasant imagery and relaxation instruction information. Shown at time of post assault medical exam.