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Impact of HIV Self-testing Among Female Sex Workers in Kampala, Uganda (HSPOT)

Primary Purpose

HIV Infection

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Oral HIV Self-Testing
Sponsored by
Harvard School of Public Health (HSPH)
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for HIV Infection focused on measuring HIV testing, Female sex workers, HIV self-testing

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • 18 years of age or older on the enrollment visit date
  • Reports exchanging sex (vaginal, anal, and/or oral) for money or goods at least once in the past month
  • Self-reported HIV negative status and no recent (<3 months) HIV testing OR self-reported HIV unknown status
  • Member of the hot spot where recruited for at least one month AND plans on remaining in the area for the next 4 months
  • Have never used an oral HIVST kit
  • Willing to participate in peer education sessions on a monthly basis over the 4-month study period and to participate in study assessments
  • Of sound mind and not under influence of drugs or coercion

Exclusion Criteria:

  • Less than 18 years of age on the enrollment date
  • Has not exchanged any form of sex in the past one month
  • Self-reported to be living with HIV
  • Self-reported HIV negative status and reports testing within the last 3 months
  • Planning to move out of geographic area within 4 months
  • Concurrently participating in another HIV prevention study
  • Meets criteria but does not wish to participate
  • Not willing or able to provide informed consent

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm Type

    Experimental

    Experimental

    No Intervention

    Arm Label

    Direct Distribution

    Fixed Distribution

    Referral to Existing Services

    Arm Description

    The direct distribution arm consists of peer educators directly distributing HIV self-test kits to participants. Peer educators will briefly describe HIV self-testing to participants but will not provide extensive training on the use of the test kit. Peer educators also provide referral to existing services for HIV testing.

    The fixed distribution arm consists of peer educators distributing coupons to participants. The participants can then use the coupon to collect an HIV self-test kit at a participating distribution point, including drug stores, pharmacies, and health posts. Peer educators will briefly describe HIV self-testing to participants but will not provide extensive training on the use of the test kit. Peer educators also provide referral to existing services for HIV testing.

    Peer educators will not provide HIV self-tests to participants. Peer educators will only provide referral to existing services for HIV testing.

    Outcomes

    Primary Outcome Measures

    HIV testing in the previous month
    HIV testing in the previous month

    Secondary Outcome Measures

    Knowledge of own HIV status
    HIV self-test kit use in the two intervention arms
    HIV self-test kit use in the two intervention arms

    Full Information

    First Posted
    July 20, 2016
    Last Updated
    May 2, 2018
    Sponsor
    Harvard School of Public Health (HSPH)
    Collaborators
    Uganda Health Marketing Group, International Research Consortium, International Initiative for Impact Evaluation
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02846402
    Brief Title
    Impact of HIV Self-testing Among Female Sex Workers in Kampala, Uganda
    Acronym
    HSPOT
    Official Title
    The Causal Impact of HIV Self-testing Among Female Sex Workers in Kampala, Uganda
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    May 2018
    Overall Recruitment Status
    Completed
    Study Start Date
    September 2016 (Actual)
    Primary Completion Date
    May 2017 (Actual)
    Study Completion Date
    June 2017 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Harvard School of Public Health (HSPH)
    Collaborators
    Uganda Health Marketing Group, International Research Consortium, International Initiative for Impact Evaluation

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    HSPOT is a cluster-randomized trial designed to determine whether HIV self-tests are acceptable and improve HIV testing rates and HIV status knowledge among female sex workers in Kampala, Uganda. This study will determine whether directly giving participants an HIV self-test or giving them a coupon to collect a test at a drug store or clinic improves outcomes compared to standard of care.
    Detailed Description
    Although Uganda has a generalized HIV epidemic, with approximately 7.4% of adults aged 15 to 49 living with HIV, the epidemic remains even more highly concentrated in key populations, including female sex workers (FSW). A particular concern for FSW is access to healthcare services, including HIV testing services. FSW face significant barriers to accessing healthcare. In other settings, evidence has suggested that stigma is a significant barrier to FSW seeking HIV testing. It is likely that similar mechanisms exist in Uganda. Evidence from Uganda has indicated that complex multilevel factors, such as stigmatization and harassment, contribute to vulnerability among FSW. User-controlled HIV prevention interventions that lead to empowerment of FSW may therefore be a powerful way to address the HIV epidemic in this key population. Oral HIV self-testing consists of an oral swab kit that allows individuals to test for HIV in the privacy of their own homes whenever they want. The ease of use of HIV self-testing, that it can be done at any time, and that is completely private may make it an attractive alternative to currently-available HIV testing mechanisms for FSW in Uganda. HIV self-testing has generally been shown to be acceptable in a variety of populations, however evidence related to its uptake and acceptability remain sparse, especially among key populations and in Sub-Saharan Africa. This research will provide rigorous evidence of the uptake and efficacy of HIV self-testing for this population. HSPOT was designed to determine whether either direct distribution of HIV self-test kits via peer educators or distribution of HIV self-tests via coupons that participants can use to collect kits at collection points such as drug stores or health posts leads to better coverage of HIV testing and better awareness of HIV status. HSPOT is a cluster-randomized trial in which peer educators recruit a small group of FSW participants, and the peer educator group is randomized to one of three study arms: 1) direct distribution of test kits, 2) fixed distribution of test kits, or 3) referral to standard of care HIV testing. The primary outcome is HIV testing in the past month measured at one and four months after the first peer educator visit (when the test kits or coupons are distributed in the intervention arms).

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    HIV Infection
    Keywords
    HIV testing, Female sex workers, HIV self-testing

    7. Study Design

    Primary Purpose
    Diagnostic
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    1:1:1 cluster randomized controlled trial
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    960 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Direct Distribution
    Arm Type
    Experimental
    Arm Description
    The direct distribution arm consists of peer educators directly distributing HIV self-test kits to participants. Peer educators will briefly describe HIV self-testing to participants but will not provide extensive training on the use of the test kit. Peer educators also provide referral to existing services for HIV testing.
    Arm Title
    Fixed Distribution
    Arm Type
    Experimental
    Arm Description
    The fixed distribution arm consists of peer educators distributing coupons to participants. The participants can then use the coupon to collect an HIV self-test kit at a participating distribution point, including drug stores, pharmacies, and health posts. Peer educators will briefly describe HIV self-testing to participants but will not provide extensive training on the use of the test kit. Peer educators also provide referral to existing services for HIV testing.
    Arm Title
    Referral to Existing Services
    Arm Type
    No Intervention
    Arm Description
    Peer educators will not provide HIV self-tests to participants. Peer educators will only provide referral to existing services for HIV testing.
    Intervention Type
    Other
    Intervention Name(s)
    Oral HIV Self-Testing
    Other Intervention Name(s)
    OraQuick HIV Self-Test
    Intervention Description
    The Oral HIV Self-Test is an in-home test that uses an oral swab to collect samples of oral mucosa that is used to detect the presence of HIV antibodies. The test is read after 20 minutes by the user. The test can be done by an individual at any time and place of the user's choosing. The test is read visually.
    Primary Outcome Measure Information:
    Title
    HIV testing in the previous month
    Time Frame
    One month from first intervention visit
    Title
    HIV testing in the previous month
    Time Frame
    Four months from first intervention visit
    Secondary Outcome Measure Information:
    Title
    Knowledge of own HIV status
    Time Frame
    Four months from first intervention visit
    Title
    HIV self-test kit use in the two intervention arms
    Time Frame
    One month from first intervention visit
    Title
    HIV self-test kit use in the two intervention arms
    Time Frame
    Four months from first intervention visit
    Other Pre-specified Outcome Measures:
    Title
    Linkage to HIV care and confirmatory testing
    Time Frame
    One month from first intervention visit
    Title
    Linkage to HIV care and confirmatory testing
    Time Frame
    Four months from first intervention visit
    Title
    HIV risk perception and beliefs about acquiring HIV
    Time Frame
    One month from first intervention visit
    Title
    HIV risk perception and beliefs about acquiring HIV
    Time Frame
    Four months from first intervention visit
    Title
    HIV disclosure with sexual partners
    Time Frame
    One month from first intervention visit
    Title
    HIV disclosure with sexual partners
    Time Frame
    Four months from first intervention visit
    Title
    Condom use with commercial sexual partners since last visit
    Time Frame
    One month from first intervention visit
    Title
    Condom use with commercial sexual partners since last visit
    Time Frame
    Four months from first intervention visit
    Title
    Condom use with non-commercial sexual partners since last visit
    Time Frame
    One month from first intervention visit
    Title
    Condom use with non-commercial sexual partners since last visit
    Time Frame
    Four months from first intervention visit
    Title
    Average number of commercial sexual partners
    Time Frame
    One month from first intervention visit
    Title
    Average number of commercial sexual partners
    Time Frame
    Four months from first intervention visit
    Title
    Average number of non-commercial sexual partners
    Time Frame
    One month from first intervention visit
    Title
    Average number of non-commercial sexual partners
    Time Frame
    Four months from first intervention visit
    Title
    Intimate partner violence, including sexual, physical, or verbal
    Time Frame
    One month from first intervention visit
    Title
    Intimate partner violence, including sexual, physical, or verbal
    Time Frame
    Four months from first intervention visit
    Title
    HIV fatalism
    Time Frame
    One month from first intervention visit
    Title
    HIV fatalism
    Time Frame
    Four months from first intervention visit
    Title
    Self-reported self-efficacy as measured by the General Self Efficacy Scale
    Time Frame
    One month from first intervention visit
    Title
    Self-reported self-efficacy as measured by the General Self Efficacy Scale
    Time Frame
    Four months from first intervention visit
    Title
    Female sex worker empowerment as measured by Beattie et al 2014
    Time Frame
    One month from first intervention visit
    Title
    Female sex worker empowerment as measured by Beattie et al 2014
    Time Frame
    Four months from first intervention visit
    Title
    Pre-exposure prophylaxis preferences
    Time Frame
    One month from first intervention visit

    10. Eligibility

    Sex
    Female
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: 18 years of age or older on the enrollment visit date Reports exchanging sex (vaginal, anal, and/or oral) for money or goods at least once in the past month Self-reported HIV negative status and no recent (<3 months) HIV testing OR self-reported HIV unknown status Member of the hot spot where recruited for at least one month AND plans on remaining in the area for the next 4 months Have never used an oral HIVST kit Willing to participate in peer education sessions on a monthly basis over the 4-month study period and to participate in study assessments Of sound mind and not under influence of drugs or coercion Exclusion Criteria: Less than 18 years of age on the enrollment date Has not exchanged any form of sex in the past one month Self-reported to be living with HIV Self-reported HIV negative status and reports testing within the last 3 months Planning to move out of geographic area within 4 months Concurrently participating in another HIV prevention study Meets criteria but does not wish to participate Not willing or able to provide informed consent
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Katrina Ortblad, MPH
    Organizational Affiliation
    Harvard School of Public Health (HSPH)
    Official's Role
    Study Director
    First Name & Middle Initial & Last Name & Degree
    Till Barnighausen, MD, ScD
    Organizational Affiliation
    Harvard School of Public Health (HSPH)
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    33138623
    Citation
    McMahon SA, Musoke DK, Wachinger J, Nakitende A, Amongin J, Nanyiri E, Turcotte-Tremblay AM, Oldenburg CE, Barnighausen T, Ortblad KF. Unintended uses, meanings, and consequences: HIV self-testing among female sex workers in urban Uganda. AIDS Care. 2021 Oct;33(10):1278-1285. doi: 10.1080/09540121.2020.1837722. Epub 2020 Nov 2.
    Results Reference
    derived
    PubMed Identifier
    30413504
    Citation
    Ortblad KF, Kibuuka Musoke D, Ngabirano T, Nakitende A, Taasi G, Barresi LG, Barnighausen T, Oldenburg CE. HIV self-test performance among female sex workers in Kampala, Uganda: a cross-sectional study. BMJ Open. 2018 Nov 8;8(11):e022652. doi: 10.1136/bmjopen-2018-022652.
    Results Reference
    derived
    PubMed Identifier
    30286737
    Citation
    Ortblad KF, Chanda MM, Musoke DK, Ngabirano T, Mwale M, Nakitende A, Chongo S, Kamungoma N, Kanchele C, Barnighausen T, Oldenburg CE. Acceptability of HIV self-testing to support pre-exposure prophylaxis among female sex workers in Uganda and Zambia: results from two randomized controlled trials. BMC Infect Dis. 2018 Oct 4;18(1):503. doi: 10.1186/s12879-018-3415-z.
    Results Reference
    derived
    PubMed Identifier
    29182634
    Citation
    Ortblad K, Kibuuka Musoke D, Ngabirano T, Nakitende A, Magoola J, Kayiira P, Taasi G, Barresi LG, Haberer JE, McConnell MA, Oldenburg CE, Barnighausen T. Direct provision versus facility collection of HIV self-tests among female sex workers in Uganda: A cluster-randomized controlled health systems trial. PLoS Med. 2017 Nov 28;14(11):e1002458. doi: 10.1371/journal.pmed.1002458. eCollection 2017 Nov.
    Results Reference
    derived

    Learn more about this trial

    Impact of HIV Self-testing Among Female Sex Workers in Kampala, Uganda

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