Clinical Trials Directory

Trials / Completed

CompletedNCT01317784

Behavioral Science Aspects of Rapid Test Acceptance

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
1,200 (actual)
Sponsor
California State University, Long Beach · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The relevance of this research to public health is to make it possible to test for hepatitis C and syphilis at point of care so that people will receive their results immediately instead of requiring people to wait for at least a week to get their test results. This research will make rapid tests for HIV available that can detect HIV infection earlier and are more accurate than current tests available in the United States.

Detailed description

This application addresses "Studies to improve access and utilization of HIV counseling and testing" for "HIV/AIDS and AIDS-related co-infections" such as "hepatitis C virus (HCV), other sexually transmitted infections (STIs)" that are part of PA-07-307 Drug Abuse Aspects of HIV/AIDS. The only rapid tests that are approved for use in the US currently are for HIV infection. Tests for other conditions such as hepatitis C (HCV) and syphilis are in use in other countries. In response to an Opportunity that the CDC published in the Federal Register, there are now candidate rapid test kits for HCV and syphilis available for experimental use in the US. Different combinations of rapid and standard tests will be offered to participants in a four-arm trial to assess which tests are accepted by the participants. Only a minority of clients at CBRS who have been offered the rapid test for HIV have accepted it. Those who chose rapid HIV tests were more likely to be male, educated, gay, young and White. They were less likely to be Black, or injection drug users. The proposed study has the potential to have a significant impact upon screening for HIV, syphilis, and HCV. Rapid tests have the potential to increase the receipt of test results, particularly among groups that are less likely to return for their results using traditional testing. The candidate tests are designed for Point of Care (either oral fluid and/or whole blood), and thus will require real-time testing, so the trial will be able to evaluate both the accuracy of the tests in settings of intended use and their acceptability to potential clients in real-world situations.

Conditions

Interventions

TypeNameDescription
DEVICERapid tests for HIV, HCV, HBV, and syphilisChoice of 16 different rapid tests. Only 12 manufacturer and names are shown because some are used with both blood and oral fluid. When they are used on both specimens, they are counted as two tests.
DEVICEHIV/HCVChoice of 10 different tests for HIV and hepatitis C.
DEVICEHIV/syphilisChoice of 7 different tests for HIV and syphilis
DEVICEHIV onlyChoice of 4 different tests for HIV only.

Timeline

Start date
2011-05-01
Primary completion
2014-06-01
Completion
2014-08-01
First posted
2011-03-17
Last updated
2015-07-29

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01317784. Inclusion in this directory is not an endorsement.