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Reducing HIV Risk Among Mexican Youth

Reducing HIV Risk Among Mexican Youth

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01084395
Enrollment
1620
Registered
2010-03-10
Start date
2002-09-30
Completion date
2006-09-30
Last updated
2010-03-19

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

Conditions

AIDS, HIV Infections, Sexually Transmitted Diseases

Keywords

Parent, Adolescent, Mexico, Safer Sex Communication, Randomized Controlled Trial, HIV/AIDS, STD, Sexual Behavior

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.

Interventions

BEHAVIORALAdolescent Safer Sex Intervention

Adolescents are randomly assigned to the HIV risk-reduction intervention condition. Adolescents receive a theory-based intervention designed to reduce HIV risk-associated behavior. The intervention consists of six 50-minute modules implemented over the course of two days. The intervention is highly interactive and includes games, videos, discussion, and role-plays.

BEHAVIORALParent Safer Sex Communication Intervention

Parents are randomly assigned to the Safer Sex Communication Intervention. Parents learn about HIV and other consequences of unprotected sexual behavior. The intervention contains content that focuses on enhancing parent-adolescent communication.

OTHERAdolescent Health Promotion Control Condition

Adolescents are randomly assigned to the Health Promotion control condition. Adolescents receive an intervention aimed at significant health problems affecting Mexicans that are related, not to sexual behavior, but to other behaviors. These health problems include heart disease, certain cancers, and diabetes. Adolescents are taught that these health problems can be prevented by changing personal behaviors, primarily exercise, diet, cigarette smoking, and alcohol and drug use.

OTHERParent Health Promotion Control Condition

Parents are randomly assigned to the Health Promotion control condition. Parents receive an intervention aimed at significant health problems affecting Mexicans that are related, not to sexual behavior, but to other behaviors. These health problems include heart disease, certain cancers, and diabetes. Parents will be taught that these health problems can be prevented by changing personal behaviors, primarily exercise, diet, cigarette smoking, and alcohol and drug use. The intervention also provides content that emphasizes the importance of families.

Sponsors

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

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

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

Design outcomes

Primary

MeasureTime frameDescription
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-upQuestions regarding this measure were asked to adolescent participants only
Intentions to Use Condoms and ContraceptivesPretest, Posttest, 6 month follow-up, 12 month follow-upQuestions regarding this measure were asked to adolescent participants only

Countries

Mexico

Outcome results

None listed

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