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Reducing HIV Risk Among Mexican Youth

Not Applicable
Completed
Conditions
HIV Infections
AIDS
Sexually Transmitted Diseases
Interventions
Behavioral: Parent Safer Sex Communication Intervention
Other: Adolescent Health Promotion Control Condition
Other: Parent Health Promotion Control Condition
Behavioral: Adolescent Safer Sex Intervention
Registration Number
NCT01084395
Lead Sponsor
University of Michigan
Brief Summary

The broad objective of this project is to test the efficacy of a theory-based HIV risk-reduction intervention, which includes both an adolescent component and parental component, designed to reduce the adolescents' risk of sexually transmitted HIV.

Detailed Description

Sexually transmitted HIV infection among adolescents is a growing and significant problem in Mexico. Given the high mortality rate associated with AIDS, the lack of available treatment, and the social stigma associated with the disease, prevention is the key to reducing the threat of AIDS among this important subgroup in Mexico. The study has four specific aims including 1) to determine whether the HIV risk-reduction intervention causes a greater increase in adolescents' intentions to abstain from intercourse and/or avoid unprotected intercourse at post-intervention and decreased self-reported intercourse and unprotected intercourse at 3, 6, 12, and 48 month follow-ups, compared with the general health promotion control intervention; 2) to determine whether the effects of the intervention are moderated by individual, microsystem, and macrosystem variables; 3) to identify theory-based variables that mediate effects of the HIV intervention on adolescents' self-reported behavior; and 4) to determine whether the HIV risk-reduction intervention causes a greater increase in parents' comfort with, and quantity of communication (general and HIV specific) with adolescents at post-intervention, 3, 6, 12, and 48 month follow-up compared with the general health promotion control intervention.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
1620
Inclusion Criteria
  • Families (adolescents [aged 14 to 17 years of age] and one of their parents)
Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Parent Safer Sex InterventionParent Safer Sex Communication Intervention-
Adolescent Health Promotion ControlAdolescent Health Promotion Control Condition-
Parent Health Promotion ControlParent Health Promotion Control Condition-
Adolescent Safer Sex InterventionAdolescent Safer Sex Intervention-
Primary Outcome Measures
NameTimeMethod
General Parent-Adolescent Communicationpretest, posttest, 6 month follow-up, 12 month follow-up
Parent-Adolescent Sexual Risk CommunicationPretest, Posttest, 6 month follow-up, 12 month follow-up
Comfort With CommunicationPretest, Posttest, 6 month follow-up, 12 month follow-up
Intentions To Have Sexual IntercoursePretest, Posttest, 6 month follow-up, 12 month follow-up

Questions regarding this measure were asked to adolescent participants only

Intentions to Use Condoms and ContraceptivesPretest, Posttest, 6 month follow-up, 12 month follow-up

Questions regarding this measure were asked to adolescent participants only

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Preparatory Schools

🇲🇽

Monterrey, NL, Mexico

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