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Behavioral Science Aspects of Rapid Test Acceptance (BSARTA)

Primary Purpose

HIV, Hepatitis C, Hepatitis B

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Rapid tests for HIV, HCV, HBV, and syphilis
HIV/HCV
HIV/syphilis
HIV only
Sponsored by
California State University, Long Beach
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional screening trial for HIV focused on measuring diagnosis screening, HIV serodiagnosis, HCV antibodies, serologic tests, Bedside testing, diagnostic test kits, syphilis serodiagnosis

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Over 17 years old
  • Mentally stable
  • Sober
  • Able to understand English or Spanish
  • At least one good vein for phlebotomy
  • Member of Behavioral Risk Group

Sites / Locations

  • Center for Behavioral Research and Services

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Active Comparator

Active Comparator

Active Comparator

Arm Label

All tests.

HIV/HCV

HIV/Syphilis

HIV only

Arm Description

Choose from all 16 possible tests.

Choice of 10 different HIV and hepatitis C tests in the bundle.

Choice of 7 different tests for HIV and syphilis.

Choice of 4 rapid tests for HIV only.

Outcomes

Primary Outcome Measures

Test choice profile
Which tests do participants choose to receive when bundled in different combinations?

Secondary Outcome Measures

Return for standard test results
Is there a different return for test results rate for the different arms of the study?

Full Information

First Posted
March 16, 2011
Last Updated
July 27, 2015
Sponsor
California State University, Long Beach
Collaborators
National Institute on Drug Abuse (NIDA)
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1. Study Identification

Unique Protocol Identification Number
NCT01317784
Brief Title
Behavioral Science Aspects of Rapid Test Acceptance
Acronym
BSARTA
Official Title
Behavioral Science Aspects of Rapid Test Acceptance
Study Type
Interventional

2. Study Status

Record Verification Date
July 2015
Overall Recruitment Status
Completed
Study Start Date
May 2011 (undefined)
Primary Completion Date
June 2014 (Actual)
Study Completion Date
August 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
California State University, Long Beach
Collaborators
National Institute on Drug Abuse (NIDA)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV, Hepatitis C, Hepatitis B, Syphilis
Keywords
diagnosis screening, HIV serodiagnosis, HCV antibodies, serologic tests, Bedside testing, diagnostic test kits, syphilis serodiagnosis

7. Study Design

Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
1200 (Actual)

8. Arms, Groups, and Interventions

Arm Title
All tests.
Arm Type
Experimental
Arm Description
Choose from all 16 possible tests.
Arm Title
HIV/HCV
Arm Type
Active Comparator
Arm Description
Choice of 10 different HIV and hepatitis C tests in the bundle.
Arm Title
HIV/Syphilis
Arm Type
Active Comparator
Arm Description
Choice of 7 different tests for HIV and syphilis.
Arm Title
HIV only
Arm Type
Active Comparator
Arm Description
Choice of 4 rapid tests for HIV only.
Intervention Type
Device
Intervention Name(s)
Rapid tests for HIV, HCV, HBV, and syphilis
Other Intervention Name(s)
INSTITM HIV-1 Antibody Test (bioLytical Laboratories, Inc.), Determine HIV-1/2 Ag/Ab Combo (Alere, Inc.), DPP® HIV 1/2 Screen Assay (Chembio, Inc.), OraQuick HCV antibody test (Orasure), DPP® HCV Screen Assay (Chembio, Inc.), DPP® HIV-HCV Screen Assay (Chembio, Inc.), Multiplo Rapid HIV/HCV Antibody Test (MedMira, Inc.), DPP® Syphilis Screen & Confirm Assay (Chembio, Inc.), DPP® HIV-Syphilis Screen Assay (Chembio, Inc.), DPP® HIV-HCV-Syphilis Screen Assay (Chembio, Inc.), Multiplo Rapid HIV/HCV/HBV Antibody Test (MedMira, Inc.)
Intervention Description
Choice 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.
Intervention Type
Device
Intervention Name(s)
HIV/HCV
Other Intervention Name(s)
INSTITM HIV-1 Antibody Test (bioLytical Laboratories, Inc.), Determine HIV-1/2 Ag/Ab Combo (Alere, Inc.), DPP® HIV 1/2 Screen Assay (Chembio, Inc.), OraQuick HCV antibody test (Orasure), DPP® HCV Screen Assay (Chembio, Inc.), DPP® HIV-HCV Screen Assay (Chembio, Inc.), Multiplo Rapid HIV/HCV Antibody Test (MedMira, Inc.)
Intervention Description
Choice of 10 different tests for HIV and hepatitis C.
Intervention Type
Device
Intervention Name(s)
HIV/syphilis
Other Intervention Name(s)
INSTITM HIV-1 Antibody Test (bioLytical Laboratories, Inc.), Determine HIV-1/2 Ag/Ab Combo (Alere, Inc.), DPP® HIV 1/2 Screen Assay (Chembio, Inc.), DPP® Syphilis Screen & Confirm Assay (Chembio, Inc.), DPP® HIV-Syphilis Screen Assay (Chembio, Inc.)
Intervention Description
Choice of 7 different tests for HIV and syphilis
Intervention Type
Device
Intervention Name(s)
HIV only
Other Intervention Name(s)
INSTITM HIV-1 Antibody Test (bioLytical Laboratories, Inc.), Determine HIV-1/2 Ag/Ab Combo (Alere, Inc.), DPP® HIV 1/2 Screen Assay (Chembio, Inc.)
Intervention Description
Choice of 4 different tests for HIV only.
Primary Outcome Measure Information:
Title
Test choice profile
Description
Which tests do participants choose to receive when bundled in different combinations?
Time Frame
one day (day one of study)
Secondary Outcome Measure Information:
Title
Return for standard test results
Description
Is there a different return for test results rate for the different arms of the study?
Time Frame
one week

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Over 17 years old Mentally stable Sober Able to understand English or Spanish At least one good vein for phlebotomy Member of Behavioral Risk Group
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dennis G Fisher, Ph.D.
Organizational Affiliation
California State University, Long Beach
Official's Role
Principal Investigator
Facility Information:
Facility Name
Center for Behavioral Research and Services
City
Long Beach
State/Province
California
ZIP/Postal Code
90813
Country
United States

12. IPD Sharing Statement

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Behavioral Science Aspects of Rapid Test Acceptance

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