Positive Lifestyles Using Safety

NCT00836290 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 90

Last updated 2015-10-21

No results posted yet for this study

Summary

Project PLUS tests an HIV risk reduction/adherence behavioral intervention with HIV-infected individuals in Connecticut prisons. Participants are randomly assigned to one of three groups: prior to release from incarceration (Group 1), after release from incarceration (Group 2), and treatment-as-usual (Group 3). We hypothesize that the intervention groups (Groups 1 \& 2) will demonstrate significantly greater knowledge regarding drug- and sex- related HIV risk behavior and HIV medication adherence, greater motivation to reduce HIV risk behavior and improve HIV medication adherence, and enhanced skills for engaging in HIV risk reduction behavior and HIV medication adherence vs. the treatment-as-usual group. We will also compare these outcomes between Groups 1 and 2.

Conditions

  • HIV
  • HIV Infections

Interventions

BEHAVIORAL

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.

BEHAVIORAL

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.

Sponsors & Collaborators

  • Centers for Disease Control and Prevention

    collaborator FED
  • National Institute on Drug Abuse (NIDA)

    collaborator NIH
  • Yale AIDS Program

    collaborator UNKNOWN
  • AIDS Project Hartford

    collaborator INDUSTRY
  • Connecticut State, Department of Correction

    collaborator UNKNOWN
  • Yale University

    lead OTHER

Principal Investigators

  • Frederick Altice, MD · Yale University

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
FACTORIAL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-01-31
Primary Completion
2010-08-31
Completion
2010-08-31

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00836290 on ClinicalTrials.gov