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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03138135
Other study ID # 16-20492
Secondary ID R01AI104309
Status Completed
Phase N/A
First received
Last updated
Start date January 9, 2017
Est. completion date November 30, 2018

Study information

Verified date April 2021
Source Public Health Foundation Enterprises, Inc.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Home HIV self-testing has been FDA approved and allows users to read their own HIV test results at home, while home sexually transmitted infection (STI) test self-collection allows men to use a swab at home and mail it in for testing. The purpose of this study is to learn how Men who have Sex with Men (MSM) use these new testing options, a set of online support tools, and the option to test with someone to support them (a testing "buddy"). We will also evaluate whether the online tools help these men to connect with HIV prevention services such as Pre-Exposure Prophylaxis (PrEP) if they test HIV negative, and to HIV care services if they test HIV positive.


Description:

Participants will be randomized 2:1 after enrollment to the intervention and control condition. Data obtained from this study will be used to inform the further tailoring and distribution of an intervention for young Black and Latino MSM to increase utilization of home HIV self-testing and linkage to HIV treatment and Pre-Exposure Prophylaxis (PrEP).


Recruitment information / eligibility

Status Completed
Enrollment 104
Est. completion date November 30, 2018
Est. primary completion date November 30, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 35 Years
Eligibility Inclusion Criteria: - Self-identify as Black or Latino. - Report anal sex with at least one male sex partner in the prior 12 months. - HIV negative by self-report. - Currently own a cell phone. - Willing and able to provide written informed consent. Exclusion Criteria: - Inadequate contact information for follow-up. - In a mutually monogamous sexual relationship for the past 12 months. - Currently taking PrEP. - Does not have reliable access to the Internet. - Does not live, work, or play in the San Francisco Bay Area. - Planning to move out of the Bay Area during the 9 month study period. - Previously participated in the HOME Pilot study. - Any medical, psychiatric, or social condition, or occupational, or other responsibility that, in the judgment of the investigator, would make participation in the study unsafe, complicate interpretation of study outcome data, or otherwise interfere with achieving the study objectives.

Study Design


Intervention

Behavioral:
HOME Study intervention
Access to home HIV test kits, home STI self-collection kits, the HOME Study website, and the SexPro HIV risk assessment tool.
Control
Counseling about the importance of quarterly HIV/STI testing and a PrEP information pamphlet.

Locations

Country Name City State
United States Bridge HIV, San Francisco Department of Public Health San Francisco California

Sponsors (4)

Lead Sponsor Collaborator
Public Health Foundation Enterprises, Inc. National Institute of Allergy and Infectious Diseases (NIAID), San Francisco Department of Public Health, University of California, San Francisco

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other Who uses home HIV self-testing and home STI self-collection. Testing and self-collection rates by occasion, age, county, race/ethnicity, and prior testing history. Aggregate descriptive analysis. 9 months
Other Who uses a buddy. Differences in testing with a buddy by occasion, age, county, race/ethnicity, and prior testing history. Aggregate descriptive analysis. 9 months
Other Use of HIV prevention services. Proportion of HIV uninfected participants who attend group or individual counseling services. 9 months
Primary Efficacy of the HOME package to support linkage to PrEP or HIV care Between-arm differences in initiation of PrEP; qualitative evaluation of linkage to HIV care. 9 months
Primary Efficacy of the HOME package to increase HIV and STI testing frequency. The proportion of participants reporting HIV and STI testing rates between visits. 9 months
Secondary Feasibility of the individual components of the study intervention. Combined analysis of overall use of study intervention: Usage of home HIV self-testing, with and without buddies, as well as STI-self collection; Proportion of participants who log-in to the HOME Study site at least once, distribution of numbers of log-ins, and use of HOME Study pages, as measured by numbers of clicks and views for each page. 9 months
Secondary Acceptability of the HOME package to support linkage to HIV care or PrEP. Acceptability scores from online questionnaires and the distribution of repeated scores at follow-up timepoints. 9 months
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