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Clinical Trials/NCT00250549
NCT00250549
Completed
Not Applicable

A Randomized Control Trial Evaluating the Educational Effectiveness of a Rapid HIV Post-Test Counseling Video.

North Bronx Healthcare Network1 site in 1 country128 target enrollmentMay 2005
ConditionsHIV

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
HIV
Sponsor
North Bronx Healthcare Network
Enrollment
128
Locations
1
Primary Endpoint
Mean Knowledge Score within both groups.
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

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.

Detailed Description

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%.

Registry
clinicaltrials.gov
Start Date
May 2005
End Date
March 2006
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

  • 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.

Outcomes

Primary Outcomes

Mean Knowledge Score within both groups.

Time Frame: One year

Secondary Outcomes

  • Overall condom intention measures and Condom Self efficacy measures(One year)

Study Sites (1)

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