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A Bundled Rapid HIV/HCV Testing Intervention to Increase Receipt of Test Results (iKnow2 Project)

Primary Purpose

Substance-related Disorders

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
On-site bundled rapid HIV/HCV testing
Standard of care (SOC)
Sponsored by
Columbia University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Substance-related Disorders focused on measuring HIV, HCV

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Report being HIV and HCV negative, or report not knowing HIV and HCV status
  • Not have received results of an HIV or HCV test initiated within the last 12 months
  • Able and willing to provide informed consent
  • Seeking or currently receiving drug (excluding alcohol only treatment) abuse treatment services at the participating treatment programs
  • At least 18 years old
  • Able to communicate in English
  • Willing to sign a release form that will allow medical record review (to corroborate self-reports of receipt of test results)
  • Able and willing to provide locator information (contact number and address) for follow-up surveys

Sites / Locations

  • Acacia Network/Promesa

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

On-site bundled rapid HIV/HCV testing

Standard of care (SOC)

Arm Description

Participants will receive the on-site bundled rapid HIV/HCV testing intervention. In the intervention group, all patients will receive an offer to participate in rapid HIV/HCV testing. Those who accept this offer will: receive pre-test information about testing procedures and education, be tested, receive results during the same visit as testing, and be provided post-test counseling and support services by trained test counselors. Patients with a preliminary positive (i.e., reactive) HIV and/or HCV test result(s) will be actively linked immediately to a health care provider for further evaluation and confirmatory HIV and/or HCV RNA testing.

Participants will receive the standard of care (SOC) at the study sites. The SOC entails venipuncture whole blood HIV testing + venipuncture whole blood HCV testing. Blood draws are sent to an external laboratory for processing, and patients must return for test results in another visit. Patients may not receive pre-test information or results and post-test counseling, especially if non-reactive or negative test result(s). Reflex testing is not standard practice, therefore some patients may require another visit and blood draw for confirmatory HIV and/or HCV RNA testing. Linkage to care in the SOC is accomplished by referral to a health care provider, either within the participating substance use disorder treatment organization or passive referral to other health facilities.

Outcomes

Primary Outcome Measures

Self-Report Receipt of HIV and Hepatitis C Test Results
The primary outcome is self-reported receipt of HIV/HCV test results. This will be measured at one-month post-randomization for all participants. We acknowledge that there are several potential HIV/HCV testing behaviors that could be evaluated in this study: acceptance of testing, completion of testing, and receipt of testing results, either HIV or HCV. Acceptance of testing measures whether or not a participant would accept the offer of an HIV or HCV test. Completion of testing measures whether or not a participant completes the HIV or HCV test. Receipt of test results refers to whether or not a participant self-reports having received the results of the HIV or HCV test.

Secondary Outcome Measures

Linkage to care (Proportion of patients who initiated HIV/HCV care before the 3-month follow-up among those whose test results were positive for HIV and/or HCV.)
Proportion of patients who initiated HIV/HCV care before the 3-month follow-up among those whose test results were positive for HIV and/or HCV.
Sexual risk behaviors (Counts of unprotected vaginal and anal sex acts in the past 3 months with any sex partner.)
Counts of unprotected vaginal and anal sex acts in the past 3 months with any sex partner.
Drug use behaviors (Prevalence of use of any drugs in the past 3 months; and unsafe injection practices.)
Prevalence of use of any drugs in the past 3 months; and unsafe injection practices.

Full Information

First Posted
January 30, 2015
Last Updated
February 21, 2018
Sponsor
Columbia University
Collaborators
New York University, Beth Israel Medical Center, National Institute on Drug Abuse (NIDA)
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1. Study Identification

Unique Protocol Identification Number
NCT02355080
Brief Title
A Bundled Rapid HIV/HCV Testing Intervention to Increase Receipt of Test Results
Acronym
iKnow2 Project
Official Title
A Bundled Rapid HIV/HCV Testing Intervention to Increase Receipt of Test Results
Study Type
Interventional

2. Study Status

Record Verification Date
February 2018
Overall Recruitment Status
Completed
Study Start Date
April 2016 (Actual)
Primary Completion Date
July 2017 (Actual)
Study Completion Date
July 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Columbia University
Collaborators
New York University, Beth Israel Medical Center, National Institute on Drug Abuse (NIDA)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a randomized controlled clinical trial in which adults receiving drug abuse treatment will be recruited to participate in a HIV and hepatitis C (HCV) testing study. The purpose of this study is to test the efficacy of two HIV/HCV testing strategies on increasing receipt of test results: (1) on-site bundled rapid HIV/HCV testing (i.e., joint offer of HIV and HCV at the point of encounter), and (2) standard of care for HIV and HCV testing.
Detailed Description
This is a randomized controlled clinical trial in which adults receiving drug abuse treatment will be recruited to participate in a HIV and hepatitis C (HCV) testing study. The purpose of this study is to test the efficacy of two HIV/HCV testing strategies on increasing receipt of test results: (1) on-site bundled rapid HIV/HCV testing (i.e., joint offer of HIV and HCV at the point of encounter), and (2) standard of care for HIV and HCV testing. Secondary outcomes include linkage to care and HIV and HCV risk behaviors. Participants will complete a baseline assessment to report their demographics, sexual risk behaviors, drug-using risk behaviors, utilization of drug abuse treatment services and will be randomized to one of two groups. At one-month post-randomization, participants will complete a follow-up assessment to determine whether or not they received their HIV or HCV test results. At three months post-randomization, participants will complete a follow-up assessment to assess linkage to care and changes, if any, in their HIV and HCV sexual risk behaviors.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Substance-related Disorders
Keywords
HIV, HCV

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
134 (Actual)

8. Arms, Groups, and Interventions

Arm Title
On-site bundled rapid HIV/HCV testing
Arm Type
Experimental
Arm Description
Participants will receive the on-site bundled rapid HIV/HCV testing intervention. In the intervention group, all patients will receive an offer to participate in rapid HIV/HCV testing. Those who accept this offer will: receive pre-test information about testing procedures and education, be tested, receive results during the same visit as testing, and be provided post-test counseling and support services by trained test counselors. Patients with a preliminary positive (i.e., reactive) HIV and/or HCV test result(s) will be actively linked immediately to a health care provider for further evaluation and confirmatory HIV and/or HCV RNA testing.
Arm Title
Standard of care (SOC)
Arm Type
Active Comparator
Arm Description
Participants will receive the standard of care (SOC) at the study sites. The SOC entails venipuncture whole blood HIV testing + venipuncture whole blood HCV testing. Blood draws are sent to an external laboratory for processing, and patients must return for test results in another visit. Patients may not receive pre-test information or results and post-test counseling, especially if non-reactive or negative test result(s). Reflex testing is not standard practice, therefore some patients may require another visit and blood draw for confirmatory HIV and/or HCV RNA testing. Linkage to care in the SOC is accomplished by referral to a health care provider, either within the participating substance use disorder treatment organization or passive referral to other health facilities.
Intervention Type
Behavioral
Intervention Name(s)
On-site bundled rapid HIV/HCV testing
Intervention Description
Participants will be offered bundled on-site rapid HIV and HCV testing with post-test counseling that addresses both sexual and drug use risk reduction, and linkage to care.
Intervention Type
Behavioral
Intervention Name(s)
Standard of care (SOC)
Intervention Description
Participants will receive the SOC for HIV and HCV testing at the study sites.
Primary Outcome Measure Information:
Title
Self-Report Receipt of HIV and Hepatitis C Test Results
Description
The primary outcome is self-reported receipt of HIV/HCV test results. This will be measured at one-month post-randomization for all participants. We acknowledge that there are several potential HIV/HCV testing behaviors that could be evaluated in this study: acceptance of testing, completion of testing, and receipt of testing results, either HIV or HCV. Acceptance of testing measures whether or not a participant would accept the offer of an HIV or HCV test. Completion of testing measures whether or not a participant completes the HIV or HCV test. Receipt of test results refers to whether or not a participant self-reports having received the results of the HIV or HCV test.
Time Frame
One month post-randomization
Secondary Outcome Measure Information:
Title
Linkage to care (Proportion of patients who initiated HIV/HCV care before the 3-month follow-up among those whose test results were positive for HIV and/or HCV.)
Description
Proportion of patients who initiated HIV/HCV care before the 3-month follow-up among those whose test results were positive for HIV and/or HCV.
Time Frame
One month post-randomization
Title
Sexual risk behaviors (Counts of unprotected vaginal and anal sex acts in the past 3 months with any sex partner.)
Description
Counts of unprotected vaginal and anal sex acts in the past 3 months with any sex partner.
Time Frame
One month post-randomization
Title
Drug use behaviors (Prevalence of use of any drugs in the past 3 months; and unsafe injection practices.)
Description
Prevalence of use of any drugs in the past 3 months; and unsafe injection practices.
Time Frame
One month post-randomization

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Report being HIV and HCV negative, or report not knowing HIV and HCV status Not have received results of an HIV or HCV test initiated within the last 12 months Able and willing to provide informed consent Seeking or currently receiving drug (excluding alcohol only treatment) abuse treatment services at the participating treatment programs At least 18 years old Able to communicate in English Willing to sign a release form that will allow medical record review (to corroborate self-reports of receipt of test results) Able and willing to provide locator information (contact number and address) for follow-up surveys
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jemima A. Frimpong, PhD, MPH
Organizational Affiliation
Columbia University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Acacia Network/Promesa
City
New York
State/Province
New York
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
26936623
Citation
Frimpong JA, D'Aunno T, Perlman DC, Strauss SM, Mallow A, Hernandez D, Schackman BR, Feaster DJ, Metsch LR. On-site bundled rapid HIV/HCV testing in substance use disorder treatment programs: study protocol for a hybrid design randomized controlled trial. Trials. 2016 Mar 3;17(1):117. doi: 10.1186/s13063-016-1225-4.
Results Reference
derived

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A Bundled Rapid HIV/HCV Testing Intervention to Increase Receipt of Test Results

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