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
NA
90 participants
INTERVENTIONAL
2008-01-31
2010-08-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
FACTORIAL
PREVENTION
NONE
Study Groups
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Pre-release
Participants in the pre-release intervention group will receive four sessions in the four-week period prior to release and will receive a comprehensive booster session four weeks after release.
Pre-Release (Group 1)
Participants in the pre-release intervention group will receive four sessions in the four-week period prior to release and will receive a comprehensive booster session four weeks after release.
Post-release
Participants in the post-release intervention group will receive one comprehensive introductory session four weeks before release and four sessions during the four-week period after release.
Post-release (Group 2)
Participants in the post-release intervention group will receive one comprehensive introductory session four weeks before release and four sessions during the four-week period after release.
Control
Participants in the control group do not receive education sessions during their term in the study. However, these sessions are available to them after completing the study.
No interventions assigned to this group
Interventions
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Pre-Release (Group 1)
Participants in the pre-release intervention group will receive four sessions in the four-week period prior to release and will receive a comprehensive booster session four weeks after release.
Post-release (Group 2)
Participants in the post-release intervention group will receive one comprehensive introductory session four weeks before release and four sessions during the four-week period after release.
Eligibility Criteria
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Inclusion Criteria
* Meet DSM-IV criteria for opioid-dependence
* Are scheduled to be released from prison within the next 30 days
* Are confirmed to be HIV-infected
* Report drug- or sex-related HIV risk behavior prior to incarceration
* Are willing to provide locator information
* Able to read and understand the questionnaires and consent form
* No minimum duration of incarceration
* Available for the full duration of the study with no anticipated circumstances impeding participation (e.g., pending court case or warrant).
Exclusion Criteria
* Suicidal or homicidal ideation
18 Years
ALL
No
Sponsors
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Centers for Disease Control and Prevention
FED
National Institute on Drug Abuse (NIDA)
NIH
Yale AIDS Program
UNKNOWN
AIDS Project Hartford
INDUSTRY
Connecticut State, Department of Correction
UNKNOWN
Yale University
OTHER
Responsible Party
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Principal Investigators
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Frederick Altice, MD
Role: PRINCIPAL_INVESTIGATOR
Yale University
Locations
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Yale AIDS Program, Yale University School of Medicine
New Haven, Connecticut, United States
Countries
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Other Identifiers
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0701002257
Identifier Type: -
Identifier Source: org_study_id
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