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Maintaining HIV Prevention Gains in Female Adolescents

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

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00161343
Enrollment
640
Registered
2005-09-12
Start date
2004-12-31
Completion date
2009-08-31
Last updated
2012-09-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV Infection, Sexually Transmitted Diseases

Keywords

HIV, Prevention Intervention, Female, Adolescents, STD, HIV Seronegativity

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.

Interventions

BEHAVIORALHealth Improvement Project for Teens on HIV Prevention

Comparison of 2 facilitator-led intervention groups: (1) HIV prevention, and (2) general health promotion. Outcome measures: sexual risk behaviors in adolescent girls

Sponsors

National Institute of Nursing Research (NINR)
CollaboratorNIH
University of Rochester
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
15 Years to 19 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frame
rates of STIsBaseline, 6 and 12 months
computer-assisted survey resultsbaseline, 1 week, 3, 6, & 12 months
- score on self-report of frequency of risky sexual and substance use behaviorsbaseline, 1 week, 3, 6, & 12 months

Secondary

MeasureTime frame
- score on assessments of information, motivation, and behavioral skills to reduce risk for HIVbaseline, 3, 6, & 12 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026