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Clinical Trials/NCT00255944
NCT00255944CompletedNot Applicable

Internet-based Efficacy Trial of an HIV Prevention Program

University of Colorado, Denver1 site in 1 country2,622 target enrollmentStarted: October 1, 2005Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
2,622
Locations
1
Primary Endpoint
Efficacy of Internet-based Program for Increasing Condom Use With Non-main Sex Partners

Study 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
18 Years to 25 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

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

Exclusion Criteria

  • Colorado resident

Arms & Interventions

Youthnet messages on Facebook

Experimental

Participants will receive internet-based messages from the Youthnet program

Intervention: Youthnet Internet-based program (Behavioral)

Messages on Facebook about current events

Active Comparator

Participants will receive internet-based messages from the control program

Intervention: Control Internet based program (Behavioral)

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)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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