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NCT01622855 · ClinicalTrials.gov registry record · Phase 1
Acute Intervention to Reduce Distress Following Sexual Assault
A Phase 1 study of Post Traumatic Stress Disorder and Drug Use, sponsored by Medical University of South Carolina.
- Completed
- Registry status
- Phase 1
- Development phase
- 442
- Enrollment target
- 1
- Study location
NCT01622855: Completed Phase 1 study of Post Traumatic Stress Disorder and Drug Use, sponsored by Medical University of South Carolina.
NCT01622855 is a Phase 1 study of Post Traumatic Stress Disorder and Drug Use that has completed, run by Medical University of South Carolina. The registered enrollment target is 442 participants, below the 662-participant average among 262 other Post Traumatic Stress Disorder trials with a reported enrollment target (33% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01622855, a Phase 1 study of Post Traumatic Stress Disorder and Drug Use, has completed, sponsored by Medical University of South Carolina.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 442 participants
- Enrollment target
- 1
- Study location
Study 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.
Primary Outcome
Number of days use of specific drugs in preceding 14 days at 6 week, 3 and 6 month follow-ups
Conditions Studied
Interventions
- BEHAVIORAL PPRS
Study Locations (1)
South Carolina
- Medical University of South Carolina - Charleston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 442 participants |
| Start Date | 1997-03 |
| Est. Completion | 2005-09 |
| Phase | Phase 1 |
What the finished NCT01622855 record still lists
NCT01622855 is an interventional study that assigns participants to a tested intervention. The registered 442 participants enrollment target is mid-sized for trials with a published cap, below the 662-participant average among 262 other Post Traumatic Stress Disorder trials with a reported enrollment target (33% lower).
The record links to 3 conditions, with Post Traumatic Stress Disorder appearing as the primary indexed condition, and to 1 intervention - of which PPRS is the first listed.
NCT01622855 reports a single indexed study location in South Carolina.
Frequently Asked Questions
What is clinical trial NCT01622855 about?
NCT01622855 is a clinical study titled "Acute Intervention to Reduce Distress Following Sexual Assault". 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 PT...
What is the current status of trial NCT01622855?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 442 participants. The study started on 1997-03. Estimated completion is 2005-09.
What conditions does trial NCT01622855 study?
This clinical trial studies the following conditions: Post Traumatic Stress Disorder, Drug Use, Drug Abuse.
What interventions are being tested in trial NCT01622855?
The interventions under investigation include: PPRS (BEHAVIORAL).
Who is sponsoring clinical trial NCT01622855?
This trial is sponsored by Medical University of South Carolina, which has 755 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01622855 being conducted?
This trial has 1 study location across South Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Where NCT01622855's enrollment target sits among peer trials
442 14th of 262 higher than 249 of 262 other Post Traumatic Stress Disorder trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Post Traumatic Stress Disorder trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
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