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Clinical Trials/NCT01084395
NCT01084395
Completed
Not Applicable

Reducing HIV Risk Among Mexican Youth

University of Michigan1 site in 1 country1,620 target enrollmentSeptember 2002

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
HIV Infections
Sponsor
University of Michigan
Enrollment
1620
Locations
1
Primary Endpoint
General Parent-Adolescent Communication
Status
Completed
Last Updated
16 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
September 2002
End Date
September 2006
Last Updated
16 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Families (adolescents \[aged 14 to 17 years of age\] and one of their parents)

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

General Parent-Adolescent Communication

Time Frame: pretest, posttest, 6 month follow-up, 12 month follow-up

Parent-Adolescent Sexual Risk Communication

Time Frame: Pretest, Posttest, 6 month follow-up, 12 month follow-up

Comfort With Communication

Time Frame: Pretest, Posttest, 6 month follow-up, 12 month follow-up

Intentions To Have Sexual Intercourse

Time Frame: Pretest, Posttest, 6 month follow-up, 12 month follow-up

Questions regarding this measure were asked to adolescent participants only

Intentions to Use Condoms and Contraceptives

Time Frame: Pretest, Posttest, 6 month follow-up, 12 month follow-up

Questions regarding this measure were asked to adolescent participants only

Study Sites (1)

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