Evaluating Post-test HIV Counseling Videos for Teens (Control)

This study has been completed.
Sponsor:
Collaborator:
Information provided by (Responsible Party):
Yvette Calderon,MD, MS, North Bronx Healthcare Network
ClinicalTrials.gov Identifier:
NCT00851539
First received: February 25, 2009
Last updated: December 9, 2014
Last verified: December 2014

February 25, 2009
December 9, 2014
June 2008
November 2008   (final data collection date for primary outcome measure)
Intention to use condoms [ Time Frame: 5 months ] [ Designated as safety issue: No ]
Participants are asked about their intention to use condoms during sexual activity over the next 5 months
intention to use condoms [ Time Frame: 5 months ] [ Designated as safety issue: No ]
Complete list of historical versions of study NCT00851539 on ClinicalTrials.gov Archive Site
Consent to rapid HIV testing [ Time Frame: Immediate ] [ Designated as safety issue: No ]
All participants are offered an HIV test but do not have to get tested to participate. We will evaluate whether the videos or counselors convince more participants to get tested for HIV.
consent to rapid HIV testing [ Time Frame: 5 months ] [ Designated as safety issue: No ]
Not Provided
Not Provided
 
Evaluating Post-test HIV Counseling Videos for Teens
Educational Effectiveness of an HIV Pretest Video for Adolescents: A Randomized Controlled Trial

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.

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.

Interventional
Not Provided
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Single Blind (Caregiver)
Primary Purpose: Prevention
  • HIV
  • HIV Infections
Behavioral: Video
Behavioral Intervention Video
  • No Intervention: Control
    Participants received counseling from a live counselor.
  • Experimental: Video
    Behavioral Intervention Video
    Intervention: Behavioral: Video
Calderon Y, Cowan E, Leu CS, Brusalis C, Rhee JY, Nickerson J, Leider J, Bauman LJ. A human immunodeficiency virus posttest video to increase condom use among adolescent emergency department patients. J Adolesc Health. 2013 Jul;53(1):79-84. doi: 10.1016/j.jadohealth.2013.01.028. Epub 2013 Apr 9.

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
200
April 2011
November 2008   (final data collection date for primary outcome measure)

Inclusion Criteria:

  1. Youth who have had vaginal, anal or oral sex
  2. 15-21 years of age
  3. English speaking

Exclusion Criteria:

  1. Clinically unstable secondary to pain or unstable vitals signs
  2. Unable to understand the consent process for the study
  3. Known HIV status or recent HIV test
  4. Language other than English
Both
15 Years to 21 Years
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00851539
2006-443, 5K23HD054315
Yes
Yvette Calderon,MD, MS, North Bronx Healthcare Network
North Bronx Healthcare Network
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Principal Investigator: Yvette Calderon, MD MS Jacobi Medical Center/ Albert Einstein Medical College
North Bronx Healthcare Network
December 2014

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP