Skip to main content
Clinical Trials/NCT00255944
NCT00255944
Completed
N/A

Internet-based Efficacy Trial of an HIV Prevention Program

University of Colorado, Denver1 site in 1 country2,622 target enrollmentOctober 2005

Overview

Phase
N/A
Intervention
Not specified
Conditions
HIV Infections
Sponsor
University of Colorado, Denver
Enrollment
2622
Locations
1
Primary Endpoint
Efficacy of Internet-based Program for Increasing Condom Use With Non-main Sex Partners
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

This 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 Sexually Transmitted Diseases (STD) infection in young adults.

Detailed Description

Adolescents and young adults are at the greatest risk for acquiring an STD. Approximately 3 million people between the ages of 18 and 24 become infected 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. This 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 1-year open-label study will be recruited exclusively via the internet. Participants will be randomly assigned to receive internet-based messages from either the Youthnet program or the control program. Messages from the Youthnet program will be interactive and tailored specifically to Human Immunodeficiency Virus/Sexually Transmitted Diseases (HIV/STD) risk reduction. The control program will deliver standard STD/HIV prevention messages. Participants will be assessed at baseline and a follow-up session 4 months after enrollment. Frequency of condom use and attitudes toward condom use will be assessed using behavioral scales.

Registry
clinicaltrials.gov
Start Date
October 2005
End Date
December 2008
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Has access to the internet
  • Has an e-mail address

Exclusion Criteria

  • Colorado resident

Outcomes

Primary Outcomes

Efficacy of Internet-based Program for Increasing Condom Use With Non-main Sex Partners

Time Frame: Month 2 post baseline

Secondary Outcomes

  • Efficacy of Internet-based Program for Increasing Condom Use Attitudes, Norms, and Intentions With Non-main Sex Partners(Month 2 post baseline)

Study Sites (1)

Loading locations...

Similar Trials