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Clinical Trials/NCT00161343
NCT00161343
Completed
Phase 2

Randomized Controlled Trial of an Group Intervention to Maintain HIV Prevention Gains in Female Adolescents

University of Rochester1 site in 1 country640 target enrollmentDecember 2004

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
HIV Infection
Sponsor
University of Rochester
Enrollment
640
Locations
1
Primary Endpoint
rates of STIs
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

In this study, an intervention is tested that is designed to reduced risky sexual behaviors in adolescent females. Study design:

  • randomized, controlled study
  • participants: 640 girls aged 15-19 years old
  • length of follow-up: 1 year after the intervention is completed

Study hypothesis: The experimental condition will significantly reduce risky sexual behaviors in adolescent females as measured by:

  • lower incidence of STI's at 6 and 12 months, as compared to baseline
  • decreased incidence of risky sexual behaviors
  • increased knowledge of the level of risk of certain behaviors
  • increased knowledge of safer sexual behaviors that can prevention HIV infection
  • increased motivation to reduce sexual risk
  • increased behavioral skills to reduce risk of HIV infection

Detailed Description

Adolescence is the only age category where the number of females infected with HIV outnumber the number of males. Despite these data, only three randomized controlled trials have evaluated the efficacy of a gender-specific HIV-risk reduction program for adolescent females. The proposed research aims to address this gap in HIV prevention science, and will evaluate the short and longer-term efficacy of a HIV-prevention intervention for adolescent girls. We will recruit 640 adolescent females aged 15 to 19 years from family planning clinics and randomly assign them to one of two conditions: (a) an HIV-risk reduction intervention based on the Information-Motivation-Behavioral Skills (IMB) model (Fisher \& Fisher, 1992) or (b) a structurally equivalent health promotion control group (CTL) both supplemented by booster sessions at 3 and 6 months. At a short-term (3-month) follow-up, we hypothesize that IMB participants will increase HIV-related knowledge, motivation, and behavioral skills, and decrease the frequency of risky sexual practices relative to CTL participants. We will reassess all participants at 6 and 12 months to evaluate the longer-term efficacy of the interventions. At these longer-term follow-ups, we hypothesize that IMB participants will demonstrate higher levels of HIV knowledge, motivation, and behavioral skills; decreased risky sexual practices; and decreased rates of STDs (Chlamydia, gonorrhea) relative to the CTL participants. The final aim of the proposed research is to determine whether the constructs in the Information-Motivation-Behavioral Skills (IMB) Model (Fisher \& Fisher, 1992), can account for variability in HIV-related behavior. We hypothesize that preventive behavior at 6 and 12 months will be a function of a participant's HIV-related information, motivation, and behavioral skills at the 3-month follow-up, and that information and motivation will be partially mediated by behavioral skills to influence the initiation and maintenance of HIV preventive behavior. The long-term intent of the proposed research is to develop a risk reduction program that can be used by community-based health organizations to reduce the risk of HIV infection among adolescent females.

Registry
clinicaltrials.gov
Start Date
December 2004
End Date
August 2009
Last Updated
13 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Dianne Morrison-Beedy

Professor

University of Rochester

Eligibility Criteria

Inclusion Criteria

  • 15-19 years old
  • Sexually active in the past 3 months
  • Available for follow-up contacts over the next 13 months
  • English speaking

Exclusion Criteria

  • Pregnant, or had a baby in the last 3 months
  • Married or living with a partner

Outcomes

Primary Outcomes

rates of STIs

Time Frame: Baseline, 6 and 12 months

computer-assisted survey results

Time Frame: baseline, 1 week, 3, 6, & 12 months

- score on self-report of frequency of risky sexual and substance use behaviors

Time Frame: baseline, 1 week, 3, 6, & 12 months

Secondary Outcomes

  • - score on assessments of information, motivation, and behavioral skills to reduce risk for HIV(baseline, 3, 6, & 12 months)

Study Sites (1)

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