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HIV InfectionsTest@HomeNCT04131465

Home HIV Testing for Older Adults in South Africa

A study testing Home HIV self-testing, Home HIV rapid testing and Home HIV self-testing and rapid testing in people with HIV Infections and Knowledge, Attitudes, Practice, run by Harvard School of Public Health (HSPH) at 1 site in South Africa.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial 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. Read more about this study

Who is it for?
Ages 40 years and olderHealthy volunteers can take part
What is being tested?
Home HIV self-testing, Home HIV rapid testing and Home HIV self-testing and rapid testing
Type of treatment
Pill or oral medicine
Could I receive a placebo?
No, everyone receives an active treatment
How many people
3,578 participants
Where
1 siteSouth Africa
Study dates
15 May 2019to Dec 2021
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 40 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • 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

Who cannot join

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

Trial locations and contacts

1 site in 1 country.

South Africa1 site
  • MRC/Wits Rural, Public Health and Health Transitions Research Unit (Agincourt)

    Acornhoek, Mpumalanga, 1360

Other trials in South Africa

About this study

Official title: Home HIV Testing for Older Adults and Their Family and Community Members: a Three-arm Randomized Controlled Trial in Rural South Africa

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.
Read the detailed description

Background In the first wave of a large population-representative study of older adults in rural South Africa, the 'Health and Aging in Africa: A Longitudinal Study of an INDEPTH Community in South Africa (HAALSI)' study, large gaps in knowledge of HIV status were found among participants, coupled with low rates of recent HIV testing and high rates of sexual behaviour that can lead to acquisition and transmission of HIV. In general, older adults should test for HIV at least once per year (HIVAge.org), but few do so, in part because current HIV testing programmes have traditionally focused on young and middle-age adults and HIV testing facilities are often difficult to access for older populations. Only 17% of older adults in the HAALSI community reported having tested for HIV in the past 6 months.

Home testing can provide a powerful approach to bring the health systems 'function' of HIV testing to older adults in rural Africa. In the routine health system, community health workers, such as the South African community care givers, could provide this 'function' on a regular basis. Home rapid HIV testing and HIV self-test kits have been intensively studied in many populations. HIV self-test kits have recently become available as over the- counter products in South Africa, after the South African Pharmacy Council (SAPC) lifted a ban on their sale in pharmacies in December 2016.

To date, however, no study has compared head-to-head different 'forms' of home testing for HIV. In this study, the investigators aim to establish the comparative effectiveness and cost-effectiveness of three different options of home HIV testing among older adults in rural South Africa: (1) home delivery of HIV self-test kits, (2) home HIV rapid testing, and (3) both home delivery of HIV self-test kits and home HIV rapid testing.

Overall, home HIV testing is likely attractive for older adults because it allows testing without having to visit a health care facility. Home delivery of HIV self-testing kits has the additional advantage that it allows HIV testing in a place and at a time of one's own choosing. Home approaches to HIV testing are particularly policy-relevant at this time, because South Africa and many other countries in sub-Saharan Africa are currently expanding in re-designing their community health worker programs, through which home HIV testing could be provided on a routine basis.

Preliminary evidence in this and in other populations have suggested that HIV testing and linkage to HIV treatment and care improve health care utilization for other non-HIV chronic care and reduce risky sexual behavior. The investigators will thus not only assess the effects of the different home HIV testing offers on HIV testing but also assess comparative effects on healthcare utilization, noncommunicable disease endpoints, and sexual behaviors.

Research Aims

This study thus aims to:

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

Study Design Participants in Wave 2 of the HAALSI study will be offered one of three options (randomly assigned 1:1:1) for home HIV testing: (1) three oral HIV self-test kits with a brief introduction to HIV self-testing (home HIV self-testing arm), (2) home rapid HIV testing and counselling (home rapid HIV testing arm), and (3) three oral HIV self-test kits with a brief introduction to HIV self-testing plus home rapid HIV testing and counselling (home HIV self-testing and HIV rapid testing arm). The brief introduction to HIV self-testing will include encouragement of both self-use and onward distribution to household and community members.

The HAALSI participants were randomized (sample ~3,600; 1,200 individuals in each of the three arms). Randomization has occurred during routine HAALSI fieldwork visits, using a pre-programmed randomization process that is integrated into the tablet-based HAALSI computer-assisted personal interview (CAPI). This randomization was completed during a three-month period between May and July 2019.

Outcome Assessment The primary outcomes (1-2) and a group of secondary outcomes (3-21) will be assessed by telephone at 9 months after randomization. Based on the timing of randomization, primary data collection will take place from February through May 2020. Then, both the primary and an expanded set of secondary outcomes including several biologically-measured secondary outcomes (1-25) will be assessed at 18-24 months, during the subsequent, planned cohort-based data collection (HAALSI Wave 3).

Power Calculation In the first wave of the HAALSI study, the proportion of people having tested for HIV in the past 6 months (which was about 17%) was measured. Assuming uniform distribution of testing over time, it would be expected that about 3% of older adults in the HAALSI population tested in the past month. Based on the HAALSI 1 data, the proportion of older adults who ever tested for HIV is 65%. Given these estimates for the endpoints in the control arm, this study is powered to detect a 3 percentage point difference in HIV testing in the past month and a 6 percentage point difference in ever testing for HIV across the three arms. For this power calculation the investigators further assumed, 20% loss to follow-up, 80% power and a significance level for rejecting the Null hypothesis of 0.0167. This significance level results from the adjustment of the standard 0.05 significance level for multiple hypothesis testing - each arm compared to each other arm - using the Holm-Bonferroni method.

Data Analyses The investigators will measure risk ratios for all the binary outcomes in this study, using modified Poisson regression implemented in generalized linear models with Poisson distribution and log link. Furthermore, the effect sizes for count outcomes using generalized linear models with negative binomial distribution and log link will be measured; the investigators will measure effect sizes for continuous outcomes using generalized linear models with normal distribution and identity link. All estimations will be adjusted for clustering of outcomes at the household level as well as for baseline values of the endpoints. Baseline values of our primary and secondary endpoints will be assessed during the baseline visit before the HAALSI participants receive the trial exposure.

Being tested
Home HIV self-testing, Home HIV rapid testing, Home HIV self-testing and rapid testing
Keywords
HIV testing, HIV status knowledge, Health system, Community health workers
Medical subject headings
HIV Infections, Behavior

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Home HIV self-testingDiagnostic test

    Offer of 3 OraQuick HIV self-test kits

  • Home HIV rapid testingDiagnostic test

    Offer of HIV rapid testing with Alere Determine HIV-1/2

  • Home HIV self-testing and rapid testingDiagnostic test

    Offer of 3 OraQuick HIV self-test kits and HIV rapid testing with Alere Determine HIV-1/2

Study groups in NCT04131465
Study groupRoleWhat they receive
Home HIV self-testingExperimentalFieldworkers will visit potential participants in their homes and offer 3 oral HIV self-testing kits with a short introduction to HIV self-testing.
Receives: Diagnostic Test: Home HIV self-testing
Home HIV rapid testingExperimentalFieldworkers will visit potential participants in their homes and offer home-based HIV rapid testing and counselling.
Receives: Diagnostic Test: Home HIV rapid testing
Home HIV self-testing and rapid testingExperimentalFieldworkers 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.
Receives: Diagnostic Test: Home HIV self-testing and rapid testing

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Ever tested for HIV

    Binary endpoint: participant has ever tested for HIV vs. has never tested for HIV

    Measured: 9 months

  2. Recent HIV testing

    Binary endpoint: participant has tested since enrollment in the HIV trial vs. participant has not tested since enrollment in the HIV trial

    Measured: 9 months

Secondary outcomes (23)
  1. Use of HIV self-test

    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

    Measured: 9 months

  2. Repeated HIV testing

    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

    Measured: 9 months

  3. HIV status knowledge

    Binary outcome: participant reports that he/she knows his/her HIV status

    Measured: 9 months

  4. Correct report of HIV status

    Binary outcome: participant correctly reports HIV status evaluated against biomarker HIV status vs. participant does not know or correctly report HIV status

    Measured: 9 months

  5. Use of home rapid HIV test

    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

    Measured: 9 months

  6. HIV testing at healthcare facility

    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

    Measured: 9 months

  7. Linkage to HIV treatment and care

    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

    Measured: 9 months

  8. Recent linkage to HIV treatment and care

    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

    Measured: 9 months

  9. Number of recent sex partners

    Count variable: number of sex partners since enrollment in the HIV trial

    Measured: 9 months

  10. Recent condom use

    Binary variable: participant has used condom with most recent sex partner vs. participant has not used condom with most recent sex partner

    Measured: 9 months

  11. Most recent sex partner was casual or anonymous

    Binary variable: most recent sex partner was casual or anonymous vs. most recent sex partner was neither casual nor anonymous

    Measured: 9 months

  12. Rapid HIV testing during HAALSI

    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

    Measured: 9 months

  13. HIV treatment uptake

    Binary outcome: participant has started HIV treatment vs. participant has not started HIV treatment

    Measured: 9 months

  14. Antihypertensive treatment

    Binary outcome: participant is currently receiving antihypertensive treatment vs. participant is currently not receiving antihypertensive treatment

    Measured: 9 months

  15. Diabetes treatment

    Binary outcome: participant currently receives diabetes treatment vs. participant currently does not receive diabetes treatment

    Measured: 9 months

  16. Satisfaction with the fieldworker visit

    Scale

    Measured: 9 months

  17. Satisfaction with the South African government and healthcare system

    Scale

    Measured: 9 months

  18. Trust in other people and healthcare providers

    Scale

    Measured: 9 months

  19. Depressive Symptoms

    CESD Scale

    Measured: 9 months

  20. Viral load

    Continuous variable: viral load

    Measured: 18-24 months

  21. Blood pressure

    Continuous outcome: blood pressure, systolic and diastolic

    Measured: 18-24 months

  22. Blood sugar

    Continous outcome: glucose or hemoglobin A1c

    Measured: 18-24 months

  23. Biological Antiretroviral Screening

    Binary Outcome: Presence of ART in blood

    Measured: 18-24 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted18 Oct 2019
  2. Study start15 May 2019
  3. Primary completion15 May 2020 (estimated)
  4. Study completionDec 2021 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Health services research
Allocation
Randomised
Intervention model
Parallel groups
Model description
This study will randomize older adults living in a rural community in South Africa to one of three trial arms.
Masking
Double blind
Who is masked
Investigator, Outcomes assessor
Enrolment
3,578 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04131465
Sponsor's protocol ID
NIH/NIA- 2P01AG041710-04
Acronym
Test@Home
Status last verified
Feb 2020
First submitted
15 Oct 2019
Last updated
21 Feb 2020
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: 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.

Publications

  • Gomez-Olive FX, Montana L, Wagner RG, Kabudula CW, Rohr JK, Kahn K, Barnighausen T, Collinson M, Canning D, Gaziano T, Salomon JA, Payne CF, Wade A, Tollman SM, Berkman L. Cohort Profile: Health and Ageing in Africa: A Longitudinal Study of an INDEPTH Community in South Africa (HAALSI). Int J Epidemiol. 2018 Jun 1;47(3):689-690j. doi: 10.1093/ije/dyx247. No abstract available.

    PubMed 29325152

Questions about this trial

What is this clinical trial studying?

A study testing Home HIV self-testing, Home HIV rapid testing and Home HIV self-testing and rapid testing in people with HIV Infections and Knowledge, Attitudes, Practice, run by Harvard School of Public Health (HSPH) at 1 site in South Africa.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 21 Feb 2020. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in South Africa. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Ever tested for HIV (time frame: 9 months). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT04131465, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 21 Feb 2020.

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