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Home HIV Testing for Older Adults in South Africa (Test@Home)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT04131465
Recruitment Status : Unknown
Verified February 2020 by Till Barnighausen, Harvard School of Public Health (HSPH).
Recruitment status was:  Active, not recruiting
First Posted : October 18, 2019
Last Update Posted : February 21, 2020
Sponsor:
Collaborators:
University of Heidelberg Medical Center
University of Witwatersrand, South Africa
Information provided by (Responsible Party):
Till Barnighausen, Harvard School of Public Health (HSPH)

Brief Summary:

Many older adults in rural South Africa still lack knowledge of their HIV status despite a high probability of infection. Older adults tend to test less for HIV because most HIV testing and prevention programs have been targeted at younger age groups. Other reasons for failure to test for HIV include frailty and lack of financial resources to travel to HIV testing centers. Home-based testing is a powerful approach to bring HIV testing services -- and HIV status knowledge -- to older adults. In real-life health systems, community health workers, such as the South African community care givers, could potentially provide home-based HIV testing on a routine basis. In this study, the investigators are trying to establish the best 'form' for the 'function' home-based HIV testing.

Specifically, the investigators aim to

  1. Establish the comparative effectiveness of three home-based HIV testing options among older adults in rural South Africa
  2. Identify spill-over effects of the different home-based HIV testing options to other adults in the households and communities of the older adults receiving the testing options
  3. Determine the comparative cost-effectiveness of the three home-based HIV testing options among older adults.

Condition or disease Intervention/treatment Phase
HIV Infections Knowledge, Attitudes, Practice Diagnostic Test: Home HIV self-testing Diagnostic Test: Home HIV rapid testing Diagnostic Test: Home HIV self-testing and rapid testing Not Applicable

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 3578 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Intervention Model Description: This study will randomize older adults living in a rural community in South Africa to one of three trial arms.
Masking: Double (Investigator, Outcomes Assessor)
Masking Description: The outcomes assessors will not know the arm assignment when they assess the outcomes. The investigators analyzing the data for the initial effect size estimations will be blinded to the arm assignment. Care providers (i.e., the fieldworkers providing the home-based HIV testing) and participants cannot be blinded to the assignment to the trial arms.
Primary Purpose: Health Services Research
Official Title: Home HIV Testing for Older Adults and Their Family and Community Members: a Three-arm Randomized Controlled Trial in Rural South Africa
Actual Study Start Date : May 15, 2019
Estimated Primary Completion Date : May 15, 2020
Estimated Study Completion Date : December 2021

Resource links provided by the National Library of Medicine

MedlinePlus related topics: HIV/AIDS

Arm Intervention/treatment
Experimental: Home HIV self-testing
Fieldworkers will visit potential participants in their homes and offer 3 oral HIV self-testing kits with a short introduction to HIV self-testing.
Diagnostic Test: Home HIV self-testing
Offer of 3 OraQuick HIV self-test kits

Experimental: Home HIV rapid testing
Fieldworkers will visit potential participants in their homes and offer home-based HIV rapid testing and counselling.
Diagnostic Test: Home HIV rapid testing
Offer of HIV rapid testing with Alere Determine HIV-1/2

Experimental: Home HIV self-testing and rapid testing
Fieldworkers will visit participants in their homes and offer 3 oral HIV self-testing kits with a short introduction to HIV self-testing as well as home-based HIV rapid testing and counselling.
Diagnostic Test: Home HIV self-testing and rapid testing
Offer of 3 OraQuick HIV self-test kits and HIV rapid testing with Alere Determine HIV-1/2




Primary Outcome Measures :
  1. Ever tested for HIV [ Time Frame: 9 months ]
    Binary endpoint: participant has ever tested for HIV vs. has never tested for HIV

  2. Recent HIV testing [ Time Frame: 9 months ]
    Binary endpoint: participant has tested since enrollment in the HIV trial vs. participant has not tested since enrollment in the HIV trial


Secondary Outcome Measures :
  1. Use of HIV self-test [ Time Frame: 9 months ]
    Binary outcome: participant has used HIV self-test since enrollment in the HIV trial vs. participant has not used an HIV self-test since enrollment in the HIV trial

  2. Repeated HIV testing [ Time Frame: 9 months ]
    Binary outcome: having tested at least twice since enrollment in the HIV trial vs. having tested once or fewer times since enrollment in the HIV trial

  3. HIV status knowledge [ Time Frame: 9 months ]
    Binary outcome: participant reports that he/she knows his/her HIV status

  4. Correct report of HIV status [ Time Frame: 9 months ]
    Binary outcome: participant correctly reports HIV status evaluated against biomarker HIV status vs. participant does not know or correctly report HIV status

  5. Use of home rapid HIV test [ Time Frame: 9 months ]
    Binary outcome: participant has used a rapid HIV test at home since enrollment in the HIV trial vs. particpant has not used rapid HIV test since enrollment in the HIV trial

  6. HIV testing at healthcare facility [ Time Frame: 9 months ]
    Binary outcome: participant has tested for HIV at a facility since enrollment in the HIV trial vs. participant has not tested for HIV at a facility since enrollment in the HIV trial

  7. Linkage to HIV treatment and care [ Time Frame: 9 months ]
    Binary outcome: participant has ever visited a facility where HIV treatment and care is available vs. participant has never visited a facility where HIV treatment and care is available

  8. Recent linkage to HIV treatment and care [ Time Frame: 9 months ]
    Binary outcome: participant has visited a facility where HIV treatment and care is available since enrollment in the HIV trial vs. participant has not visited a facility where HIV treatment and care is available since enrollment in the HIV trial

  9. Number of recent sex partners [ Time Frame: 9 months ]
    Count variable: number of sex partners since enrollment in the HIV trial

  10. Recent condom use [ Time Frame: 9 months ]
    Binary variable: participant has used condom with most recent sex partner vs. participant has not used condom with most recent sex partner

  11. Most recent sex partner was casual or anonymous [ Time Frame: 9 months ]
    Binary variable: most recent sex partner was casual or anonymous vs. most recent sex partner was neither casual nor anonymous

  12. Rapid HIV testing during HAALSI [ Time Frame: 9 months ]
    Binary outcome: participant used a rapid HIV test as part of the field operations of the mother study (HAALSI) since enrollment in the HIV trial vs. participant did not use an HIV test as part of the mother study since enrollment in the HIV trial

  13. HIV treatment uptake [ Time Frame: 9 months ]
    Binary outcome: participant has started HIV treatment vs. participant has not started HIV treatment

  14. Antihypertensive treatment [ Time Frame: 9 months ]
    Binary outcome: participant is currently receiving antihypertensive treatment vs. participant is currently not receiving antihypertensive treatment

  15. Diabetes treatment [ Time Frame: 9 months ]
    Binary outcome: participant currently receives diabetes treatment vs. participant currently does not receive diabetes treatment

  16. Satisfaction with the fieldworker visit [ Time Frame: 9 months ]
    Scale

  17. Satisfaction with the South African government and healthcare system [ Time Frame: 9 months ]
    Scale

  18. Trust in other people and healthcare providers [ Time Frame: 9 months ]
    Scale

  19. Depressive Symptoms [ Time Frame: 9 months ]
    CESD Scale

  20. Viral load [ Time Frame: 18-24 months ]
    Continuous variable: viral load

  21. Blood pressure [ Time Frame: 18-24 months ]
    Continuous outcome: blood pressure, systolic and diastolic

  22. Blood sugar [ Time Frame: 18-24 months ]
    Continous outcome: glucose or hemoglobin A1c

  23. Biological Antiretroviral Screening [ Time Frame: 18-24 months ]
    Binary Outcome: Presence of ART in blood



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


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Ages Eligible for Study:   40 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Participants need to be part of the second wave of a population-representative longitudinal study in rural South Africa: "Health and Aging in Africa: A Longitudinal Study of an INDEPTH community in South Africa" (HAALSI)
  • Mental capacity to consent to participation in this study

Exclusion Criteria:

  • Participants who meet the inclusion criteria but do not wish to participate in this study

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04131465


Locations
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South Africa
MRC/Wits Rural, Public Health and Health Transitions Research Unit (Agincourt)
Acornhoek, Mpumalanga, South Africa, 1360
Sponsors and Collaborators
Harvard School of Public Health (HSPH)
University of Heidelberg Medical Center
University of Witwatersrand, South Africa
Investigators
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Principal Investigator: Till Bärnighausen, MD Harvard School of Public Health (HSPH)
Publications:
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Responsible Party: Till Barnighausen, Adjunct Professor of Global Health, Harvard School of Public Health (HSPH)
ClinicalTrials.gov Identifier: NCT04131465    
Other Study ID Numbers: NIH/NIA- 2P01AG041710-04
First Posted: October 18, 2019    Key Record Dates
Last Update Posted: February 21, 2020
Last Verified: February 2020
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Yes
Plan Description: De-identified individual data for all primary and secondary outcome measures will be made available. Investigators from institutions outside those listed in this registration will be requested to obtain ethics permissions or exemptions for any analyses using these data from their institutional review boards.
Supporting Materials: Study Protocol
Statistical Analysis Plan (SAP)
Informed Consent Form (ICF)
Time Frame: Data will be available within 12 months of study completion.
Access Criteria: Data access requests will be reviewed by the publication committee of the mother study (HAALSI). Requestors will be required to sign a Data Access Agreement.

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Till Barnighausen, Harvard School of Public Health (HSPH):
HIV testing
HIV status knowledge
Health system
Community health workers
Additional relevant MeSH terms:
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HIV Infections
Blood-Borne Infections
Communicable Diseases
Infections
Sexually Transmitted Diseases, Viral
Sexually Transmitted Diseases
Lentivirus Infections
Retroviridae Infections
RNA Virus Infections
Virus Diseases
Genital Diseases
Urogenital Diseases
Immunologic Deficiency Syndromes
Immune System Diseases