Improving HIV Testing, Linkage, and Retention in Care for Men Through U=U Messaging

Sponsor
Desmond Tutu HIV Foundation (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05602376
Collaborator
National Institute of Mental Health (NIMH) (NIH), National Institutes of Health (NIH) (NIH), University of Pennsylvania (Other)
23,188
2
3
51.9
11594
223.3

Study Details

Study Description

Brief Summary

This study will evaluate the impact of U=U messaging and counseling on gaps in the HIV care cascade for men, including testing uptake and ART initiation (Aim 1), achieving viral suppression and retention in care (Aim 2) in two provinces in South Africa. The U=U message communicates the compelling idea that PLHIV who take ART and have an undetectable viral load (<200 copies/mL) cannot sexually transmit HIV. Additionally, the investigators will conduct a multi-method evaluation to inform future implementation of U=U messaging interventions (Aim 3).

Condition or Disease Intervention/Treatment Phase
  • Behavioral: U=U testing messaging scripts
  • Behavioral: U=U adherence messaging scripts
N/A

Detailed Description

Increasing the coverage of HIV testing and treatment among people living with HIV (PLHIV) is essential for ending the global AIDS epidemic. Unfortunately, compared to women, men living with HIV (MLHIV) are less likely to know their HIV status, start anti retroviral treatment, or achieve viral suppression. Given that new HIV infections among women are driven, in part, by men's testing and treatment gaps, reducing the gender gap in testing uptake, treatment initiation and achievement of viral suppression by men must be prioritized in order to accelerate the decline in HIV incidence among women, improve men's HIV-related health outcomes and achieve the UNAIDS 95-95-95 goals by 2030.

In this study, the investigators evaluate the effectiveness of Undetectable Equals Untransmittable or "U=U" messaging for closing the gender gap in the HIV cascade. Particularly for men, the U=U message has the potential to accelerate progress towards the 95-95-95 targets by: 1) reducing anxiety associated with HIV testing (1st 95); 2) encouraging people who test HIV positive to initiate ART (2nd 95); and 3) reducing fear of transmitting HIV to sexual partners by promoting treatment adherence to achieve viral suppression (3rd 95). While there is a growing knowledge of Treatment as Prevention (TasP)/U=U among PLWH in Western countries, the reach and penetration of the U=U message in sub-Saharan Africa has been limited and few studies have tested the impacted of accessible U=U messages on ART uptake and adherence in sub-Saharan Africa.

Building on the investigators prior work on U=U messaging informed by behavioral economics and human-centered design, they propose to conduct two hybrid type 1 effectiveness-implementation randomized controlled trials to evaluate the impact of U=U messages on men's uptake of community-based HIV testing and treatment initiation (Aim 1), and achievement of viral suppression (Aim 2). The investigators will also conduct a multi-method evaluation to inform future implementation of U=U messaging interventions. To improve the generalizability of the findings, the study will be conducted in two provinces in South Africa (Western and Eastern Cape). If effective, the intervention can shape global HIV testing and treatment counselling guidelines and practices. The expert, multi-institutional collaborations will allow for the application of previous research findings, leverage unique implementation platforms and resources, and rapidly disseminate the findings.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
23188 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Two hybrid type 1 effectiveness-implementation randomized controlled trials to evaluate the impact of U=U messages on men's uptake of community-based HIV testing and treatment initiation (Aim 1), and achievement of viral suppression (Aim 2)Two hybrid type 1 effectiveness-implementation randomized controlled trials to evaluate the impact of U=U messages on men's uptake of community-based HIV testing and treatment initiation (Aim 1), and achievement of viral suppression (Aim 2)
Masking:
Double (Investigator, Outcomes Assessor)
Masking Description:
Aim 1: Site-testing-days will be randomised 1:1 to implement either U=U (intervention) or SoC (Control) messaging scripts for both invitation-to-test and ART initiation. Aim 2: Randomization will be stratified by the 6 study clinics, to account for possible differences in the baseline viral loads of the catchment area populations initiating ART within each clinic with individual-level randomization will be used with random block sizes.
Primary Purpose:
Health Services Research
Official Title:
Improving HIV Testing, Linkage, and Retention in Care for Men Through U=U Messaging
Anticipated Study Start Date :
Feb 1, 2023
Anticipated Primary Completion Date :
Dec 31, 2026
Anticipated Study Completion Date :
May 31, 2027

Arms and Interventions

Arm Intervention/Treatment
Experimental: U=U testing messaging scripts

Aim 1: Human-centred designed, behavioural nudge theory informed U=U messaging intervention to improve HIV testing uptake by men

Behavioral: U=U testing messaging scripts
On site testing days randomized to the intervention, trained health promoters employed by the mobile testing venues will use U=U messaging scripts to invite men in the vicinity to seek HIV testing services on that day. On intervention days, the U=U messaging will also be used by counselors at the testing venue when referring those who test HIV positive to clinic-based ART initiation services provided by the local Department of Health

Experimental: U=U adherence messaging scripts

Aim 2: Human-centred designed, behavioural nudge theory informed U=U messaging intervention to improve ART adherence, HIV viral suppression and retention in care

Behavioral: U=U adherence messaging scripts
After receiving standard ART initiation and adherence counselling from a DoH clinic nurse per South African National Guidelines, RCs will deliver a U=U message and hand participants a small business card with a brief U=U message on it. Participants will then receive monthly SMS booster messages (but can opt out) and monthly in-clinic booster messages during routine medical refill visits, again with a business card for messaging reinforcement.

No Intervention: Standard of Care (SoC) messaging

Aim 1: SoC messaging scripts will be used to both invite men for CB-HTS and to refer those that test HIV-positive for DoH clinic-based ART initiation Aim 2: SoC messaging as part of ART initiation counselling, and as part of their HIV care and treatment program

Outcome Measures

Primary Outcome Measures

  1. ART initiation among those invited to test for HIV [30-day follow-up period]

    Proportions of ART initiation among all people invited to test in each study arm over the year of Aim 1 data collection

  2. Proportion with viral load suppression [6-month visit]

    Proportions of people who have documented viral suppression at the 6-month visit in each study arm during Aim 2

Secondary Outcome Measures

  1. % who agree to testing [Baseline]

    Proportions of testing uptake among all people invited to test in each study arm over the year of Aim 1 enrolment.

  2. Proportion retained in care [12-month visit]

    Proportions of people who have a recorded viral load at their 12-month visit in each study arm during Aim 2.

Eligibility Criteria

Criteria

Ages Eligible for Study:
15 Years and Older
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
AIM 1:
  1. male

  2. aged ≥15 years

  3. present a study issued invitation card to site receptionist

  4. ability to provide informed consent.

AIM 2:
  1. cis-gender men

  2. aged ≥15 years

  3. newly initiating ART (i.e., treatment naïve) or re-initiating ART after 6 months of being lost-to-care

  4. live in Buffalo City or Cape Town Metro Health Districts

  5. provide written informed consent

Contacts and Locations

Locations

Site City State Country Postal Code
1 Buffalo City Metro East London Eastern Cape South Africa 5217
2 Cape Town Metro Cape Town Western Cape South Africa 7405

Sponsors and Collaborators

  • Desmond Tutu HIV Foundation
  • National Institute of Mental Health (NIMH)
  • National Institutes of Health (NIH)
  • University of Pennsylvania

Investigators

  • Principal Investigator: Andrew Medina-Marino, PhD, Desmond Tutu Health Foundation
  • Principal Investigator: Alison Buttenheim, PhD, MBA, Penn Nursing and Perelman School of Medicine, University of Pennsylvania

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Desmond Tutu HIV Foundation
ClinicalTrials.gov Identifier:
NCT05602376
Other Study ID Numbers:
  • R01MH129223
  • R01MH129223
First Posted:
Nov 2, 2022
Last Update Posted:
Nov 2, 2022
Last Verified:
Oct 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Desmond Tutu HIV Foundation
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 2, 2022