HIV Infections Clinical Trial
Official title:
Randomized Controlled Trial to Establish Efficacy of a Website to Promote Condom Use for Adults Aged 18-25
This study will develop and evaluate the effectiveness of tailored web-based messages in promoting condom use among young adults.
Adolescents and young adults are at the greatest risk for acquiring a sexually transmitted
disease (STD). Approximately 3 million people between the ages of 18 and 24 become infected
with an STD each year. Education about the risks and consequences of unprotected sex is a
powerful tool that can be used to prevent or reduce the risk of infection. The program in
this study will deliver messages to educate participants about condom use and the risk of
STD infection. The study will evaluate the effectiveness of a tailored interactive online
risk reduction program versus a standard online risk reduction program in reducing the risk
of STD infection in young adults.
Participants in this open-label study will be recruited from one of two clinics in the
Denver, Colorado area: Denver Metropolitan Health Clinic or Planned Parenthood of the Rocky
Mountains. Participants will be randomly assigned to receive internet-based messages from
either the Youthnet program or the control program while filling out a risk assessment
survey. Participants in the Youthnet program will be asked their gender and ethnicity so
they may be assigned to a role model of the same gender and ethnicity via a computer
program. This role model will appear online 5 times during the survey to deliver interactive
messages that will be tailored to HIV/STD risk reduction and will specifically address
attitudes about condom usage. The control program will deliver 5 general, non-tailored
messages containing information on reproductive health not specific to condoms or STDs.
Participants will be assessed at baseline and a follow-up session 3 months after enrollment.
Frequency of condom use and attitudes toward condom use will be assessed using behavioral
scales.
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention
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