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A Theory Based HIV Prevention Video For Rapid HIV Testing: A Randomized Trial

The recruitment status of this study is unknown because the information has not been verified recently.
Verified May 2005 by North Bronx Healthcare Network.
Recruitment status was  Active, not recruiting
Sponsor:
Information provided by:
North Bronx Healthcare Network
ClinicalTrials.gov Identifier:
NCT00250549
First received: November 7, 2005
Last updated: November 16, 2005
Last verified: May 2005

November 7, 2005
November 16, 2005
May 2005
Not Provided
Mean Knowledge Score within both groups.
Same as current
Complete list of historical versions of study NCT00250549 on ClinicalTrials.gov Archive Site
Overall condom intention measures and Condom Self efficacy measures
Same as current
Not Provided
Not Provided
 
A Theory Based HIV Prevention Video For Rapid HIV Testing: A Randomized Trial
Not Provided

OraQuick is a safe, rapid test that accurately identifies HIV in as little as 20 minutes. By providing an accurate, quick method for detecting a person’s serostatus and access to immediate post-test counseling, rapid testing has a crucial role in identifying HIV status and improving post-test counseling rates in populations who are at high risk of HIV infection and high failure to return rates. This prospective randomized control trial compared the educational effectiveness of a fifteen-minute post-test counseling video with the normal practice of a session with an HIV counselor.

A convenience sample of stable patients presenting to the walk-in section of the Jacobi Medical Center Adult ED were recruited for rapid HIV testing. After consenting for the rapid HIV test and completing measures on condom intention and condom use self-efficacy, participants were randomized to either a fifteen-minute HIV post-test educational video available in English or to an HIV counselor for post-test counseling. Afterwards, both groups completed a measure of HIV knowledge assessing relevant testing information and level of satisfaction. An equivalence analysis was carried out to assess whether the video was at least as good as counseling, measured by total score on the knowledge questionnaire, with a lower equivalence bound of -5%.

Interventional
Not Provided
Allocation: Randomized
Endpoint Classification: Bio-equivalence Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Prevention
Rapid HIV Testing
Behavioral: Post test video
Not Provided
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Active, not recruiting
130
October 2005
Not Provided

Inclusion Criteria:

  • All adult patients presenting to the Urgent Care Area at Jacobi Medical Center

Exclusion Criteria:

  • Patients that were in to much pain, unable to understand the consent process or spoke another language other than the languages offered via the video or were HIV tested with in 6 months.
Both
18 Years and older
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00250549
03-190
Not Provided
Not Provided
North Bronx Healthcare Network
Not Provided
Principal Investigator: Yvette Calderon, MD, MS Jacobi Medical Center
North Bronx Healthcare Network
May 2005

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