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Effectiveness of an Online Prevention Program in Reducing the Risk of STD Infection in Young Adults (Youthnet suppl)
This study is ongoing, but not recruiting participants.
Sponsored by: National Institute of Mental Health (NIMH)
Information provided by: National Institute of Mental Health (NIMH)
ClinicalTrials.gov Identifier: NCT00255944
  Purpose

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.


Condition Intervention Phase
HIV Infections
Sexually Transmitted Diseases
Behavioral: Youthnet Internet-based program
Behavioral: Control Internet based program
Phase I
Phase II

MedlinePlus related topics: AIDS Sexually Transmitted Diseases
U.S. FDA Resources
Study Type: Interventional
Study Design: Prevention, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study
Official Title: Internet-Based Efficacy Trial of an HIV Prevention Program

Further study details as provided by National Institute of Mental Health (NIMH):

Primary Outcome Measures:
  • Efficacy of internet-based program for increasing condom use with non-main sex partners [ Time Frame: Measured at baseline and Month 2 ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Efficacy of internet-based program for increasing condom use attitudes, norms, and intentions with non-main sex partners [ Time Frame: Measured at baseline and Month 2 ] [ Designated as safety issue: No ]

Estimated Enrollment: 1860
Study Start Date: October 2005
Estimated Study Completion Date: December 2008
Estimated Primary Completion Date: November 2008 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
1: Experimental
Participants will receive internet-based messages from the Youthnet program
Behavioral: Youthnet Internet-based program
Messages from the Youthnet program will be interactive and tailored specifically to HIV/STD risk reduction. Participants will be exposed to five flash computer vignettes of 30 seconds each, concerning condom attitudes, norms self-efficacy, and risk awareness.
2: Active Comparator
Participants will receive internet-based messages from the control program
Behavioral: Control Internet based program
The control program will deliver standard STD/HIV prevention messages.

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 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.

  Eligibility

Ages Eligible for Study:   18 Years to 25 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

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

Exclusion Criteria:

  • Colorado resident
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00255944

Locations
United States, Maryland
Internet-Based, accessible from anywhere
Bethesda, Maryland, United States, 20892
Sponsors and Collaborators
Investigators
Principal Investigator: Sheana Bull, PhD University of Colorado at Denver and Health Sciences Center
  More Information

Responsible Party: University of Colorado at Denver and Health Sciences Center ( Sheana Bull, PhD, MPH, Associate Professor )
Study ID Numbers: R01 MH63690-03, DAHBR 9A-ASI
Study First Received: November 16, 2005
Last Updated: October 28, 2008
ClinicalTrials.gov Identifier: NCT00255944  
Health Authority: United States: Federal Government

Keywords provided by National Institute of Mental Health (NIMH):
HIV Prevention
Internet Intervention
STDs

Study placed in the following topic categories:
Genital Diseases, Female
Virus Diseases
Sexually Transmitted Diseases, Viral
HIV Infections
Acquired Immunodeficiency Syndrome
Sexually Transmitted Diseases
Genital Diseases, Male
Retroviridae Infections
Immunologic Deficiency Syndromes

Additional relevant MeSH terms:
Communicable Diseases
RNA Virus Infections
Slow Virus Diseases
Immune System Diseases
Lentivirus Infections
Infection

ClinicalTrials.gov processed this record on January 16, 2009