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Clinical Trials/NCT00851539
NCT00851539
Completed
Not Applicable

Educational Effectiveness of an HIV Pretest Video for Adolescents: A Randomized Controlled Trial

North Bronx Healthcare Network1 site in 1 country200 target enrollmentJune 2008

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
HIV
Sponsor
North Bronx Healthcare Network
Enrollment
200
Locations
1
Primary Endpoint
Intention to use condoms
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

The design of this randomized controlled trial (RCT) is to test the effectiveness of a post-test behavioral video in educating adolescents about HIV transmission and affecting their intentions to engage in risk-reduction behavior.

Detailed Description

Adolescents are at risk for HIV because of their engagement in high risk sexual activity. This study seeks to determine effective ways to educate teens about HIV and how to protect themselves by use of multimedia. All eligible participants who agree to enroll in this trial will be randomized into two arms: the behavioral intervention video (intervention group) or meeting with an in-person counselor (control group) as they wait for their rapid HIV results. The goals of the RCT involve establishing the feasibility of using touch-screen technology for teenagers in the ED; establishing the receptivity of teens to HIV rapid testing in the ED; providing data on rates, and obtaining preliminary data on the effectiveness of the video in changing condom efficacy, condom outcome expectancies and condom use intention. Consenting to rapid HIV testing is a secondary outcome.

Registry
clinicaltrials.gov
Start Date
June 2008
End Date
April 2011
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
North Bronx Healthcare Network
Responsible Party
Principal Investigator
Principal Investigator

Yvette Calderon,MD, MS

Professor of Clinical Emergency Medicine

North Bronx Healthcare Network

Eligibility Criteria

Inclusion Criteria

  • Youth who have had vaginal, anal or oral sex
  • 15-21 years of age
  • English speaking

Exclusion Criteria

  • Clinically unstable secondary to pain or unstable vitals signs
  • Unable to understand the consent process for the study
  • Known HIV status or recent HIV test
  • Language other than English

Outcomes

Primary Outcomes

Intention to use condoms

Time Frame: 5 months

Participants are asked about their intention to use condoms during sexual activity over the next 5 months

Secondary Outcomes

  • Consent to rapid HIV testing(Immediate)

Study Sites (1)

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