A Video-Based HCV Curriculum for Active Injection Drug Users
Cooperative Agreement to Develop, Implement, and Evaluate Viral Hepatitis and Training
2 other identifiers
interventional
103
1 country
1
Brief Summary
The investigators hypothesize that a well-designed hepatitis C (HCV) video education curriculum for active drug injectors will lead to measurable improvements in HCV testing rates, HAV and HBV vaccination rates, as well as knowledge and attitudes about this condition. The investigators will use a short 10 minute video designed for active drug users to and assess its impact vs. a usual-care counseling intervention. The investigators will measure and compare its impact at baseline, 4 weeks after video viewing, and 12 weeks after intervention.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Nov 2005
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
October 18, 2005
CompletedFirst Posted
Study publicly available on registry
October 19, 2005
CompletedStudy Start
First participant enrolled
November 1, 2005
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2007
CompletedStudy Completion
Last participant's last visit for all outcomes
August 1, 2007
CompletedDecember 9, 2008
December 1, 2008
1.7 years
October 18, 2005
December 8, 2008
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
HCV testing rates, intervention vs. usual care
HAV vaccination rates, intervention vs. usual care
HBV vaccination rates, intervention vs. usual care
Secondary Outcomes (3)
Improvement in knowledge, intervention vs. usual care
Improvement in attitudes toward behavior change, intervention vs. usual care
Improvement in motivations toward behavior change, intervention vs. usual care
Interventions
Eligibility Criteria
You may qualify if:
- Age 18 and older
- Attendance at syringe exchange program
You may not qualify if:
- Unable to provide informed consent
- Not interested in study
- Not able to speak or understand English
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
HEPPAC
Oakland, California, 94601, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Diana L. Sylvestre, MD
Organization to Achieve Solutions in Substance Abuse (OASIS)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
October 18, 2005
First Posted
October 19, 2005
Study Start
November 1, 2005
Primary Completion
August 1, 2007
Study Completion
August 1, 2007
Last Updated
December 9, 2008
Record last verified: 2008-12