Clinical Trial Details
— Status: Completed
Administrative data
NCT number |
NCT04504357 |
Other study ID # |
H-40706 |
Secondary ID |
R34MH122323 |
Status |
Completed |
Phase |
N/A
|
First received |
|
Last updated |
|
Start date |
November 21, 2022 |
Est. completion date |
February 15, 2024 |
Study information
Verified date |
February 2024 |
Source |
Boston University |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Interventional
|
Clinical Trial Summary
The near-elimination of HIV transmission with antiretroviral therapy (ART) has provided the
world with a clear path to end the HIV epidemic through the mass provision of ART at
diagnosis, i.e. test-and-treat. Despite the substantial prevention benefits of ART, the
investigators found minimal knowledge of treatment-as-prevention (TasP) in two
population-based surveys recently conducted in South Africa. In addition, current public
health messaging and clinical HIV counselling in South Africa do not emphasize the prevention
benefits of ART.
In this formative research study the investigators will develop an app-based educational
video intervention that will provide information on Undetectable = Untransmittable (U=U) that
is locally-appropriate and can be integrated into routine HIV counselling. The intervention
will be piloted in a clinical trial of patients in South Africa receiving HIV post-test and
adherence counselling services, to determine feasibility and acceptability, impact on U=U
knowledge and attitudes, impact on stigma and psychological well being, and preliminary
evidence for ART uptake and adherence.
The study builds on a longstanding collaboration between Boston University and the Health
Economics and Epidemiology Research Office (HE2RO) at the University of Witwatersrand in
Johannesburg, South Africa. The study is highly innovative because the investigators take a
novel approach - disseminating information on the prevention benefits of ART - to improve the
wellbeing of people living with HIV (PLWH) and motivate early uptake of ART in South Africa.
The investigators hypothesize that disseminating treatment-as-prevention on its merits could
substantially improve the wellbeing of PLWH and increase demand for ART, enabling countries
to maximize the impact of test-and-treat.
Description:
Phase 1- A video-based "app" will be developed to provide HIV patients with information on
TasP/U=U. The investigators will design a series of short video modules on the prevention
benefits of ART leading to viral suppression and package them as a tablet-based app to
augment existing HIV counseling. In collaboration with the Prevention Access Campaign,
locally-appropriate videos will be developed on (a) the science of TasP/U=U including risks,
(b) benefits to self (e.g. psychological benefits, ability to have children), (c) benefits to
partners (e.g. secondary prevention), (d) benefits to society (e.g. AIDS-free generation),
and (e) TasP self-efficacy, including viral load (VL) literacy, disclosure, and couples
testing. Content will be developed with HIV counselors, PLWH, and other stakeholders in an
Intervention Mapping exercise. After training clinic staff, the videos will be shown in
clinic waiting rooms and the web "app" will be integrated into HIV counseling sessions, to be
shown to patients using tablets. Intervention content will also be pushed to participants via
SMS, and the web "app" will be shared with those with any device with a web browser
application. We will conduct three formative focus groups (n=27) and formative key interviews
(n=27) with PLWHIV. The intervention will be pre-tested in two focus groups (n=17). (NOTE:
THE RESPONDENTS FOR PHASE 1 ARE NOT INCLUDED IN CLINICAL TRIAL REPORTING.)
Phase 2- A clinical trial will be conducted using two recruitment periods at three public
sector clinics to establish intervention acceptability, effects on knowledge and attitudes,
and preliminary impact on ART uptake, adherence, and viral suppression in a pilot trial and
demonstration project (n=135).
During recruitment period 1 (n=90), patients completing HIV post-test or adherence counseling
will be referred to study staff and randomized 1:1 to no intervention (Arm A) vs. "controlled
exposure" to the tablet-based U=U app (Arm B). In recruitment period 2 (n=45), U=U videos
will be shown in clinic waiting rooms and the tablet-based app will be integrated into
routine counseling (Arm C) in a "clinical exposure" demonstration project.
Participants in Arms B and C will also receive monthly text messages reinforcing intervention
content. The order of the messages will be randomized to ascertain whether different messages
were better at driving engagement with the App. Respondents will be free to opt out of these
text messages. For all study arms, investigators will assess feasibility and acceptability,
resonance of different key messages and videos, knowledge and attitudes related to TasP,
internalized stigma and mental health, HIV prevention altruism, and behaviours related to
disclosure, risk-taking, and care-seeking in surveys at enrolment, post-test, and 6 months.
ART uptake, appointment adherence, and 6-month VL will be assessed in clinical records.
Qualitative exit interviews will be conducted with participants and clinic staff (n=30).
In addition to the primary and secondary outcomes specified below, we will assess for effect
modification in primary outcomes by key constructs of our theoretical model including
baseline awareness of TasP; baseline altruistic motivations; and baseline behavioral skills
associated with TasP.