Acute Intervention to Reduce Distress Following Sexual Assault
NCT ID: NCT01622855
Last Updated: 2015-04-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE1/PHASE2
442 participants
INTERVENTIONAL
1997-03-31
2005-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
DOUBLE
Study Groups
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PPRS video
Prevention of post sexual assault stress
PPRS
Video including psycho-education and modeling of adaptive behavioral coping strategies for use post-assault.
Standard care
Receipt of standard services
No interventions assigned to this group
Interventions
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PPRS
Video including psycho-education and modeling of adaptive behavioral coping strategies for use post-assault.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Active suicidality
* Cognitive impairment
* Non-English speaking
* Severe injury
14 Years
90 Years
FEMALE
No
Sponsors
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National Institute on Drug Abuse (NIDA)
NIH
Medical University of South Carolina
OTHER
Responsible Party
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Principal Investigators
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Heidi Resnick, Ph.D.
Role: PRINCIPAL_INVESTIGATOR
Medical University of South Carolina
Locations
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Medical University of South Carolina
Charleston, South Carolina, United States
Countries
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Other Identifiers
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NCT11158
Identifier Type: -
Identifier Source: org_study_id
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