Randomized Trial of Dynamic Choice HIV Prevention at Antenatal and Postnatal Care Clinics in Rural Uganda and Kenya

Author:

Kabami Jane12ORCID,Koss Catherine A.3,Sunday Helen1,Biira Edith1,Nyabuti Marilyn4,Balzer Laura B.5,Gupta Shalika5,Chamie Gabriel3,Ayieko James4,Kakande Elijah1,Bacon Melanie C.6,Havlir Diane3,Kamya Moses R.12,Petersen Maya5,

Affiliation:

1. Infectious Diseases Research Collaboration, Kampala, Uganda;

2. Department of Medicine, Makerere University, Kampala, Uganda;

3. Department of Medicine, University of California, San Francisco, CA;

4. Center for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya;

5. Divisions of Biostatistics and Epidemiology, School of Public Health, University of California, Berkeley, CA; and

6. Department of Health and Human Services, National Institute of Health, Bethesda, MD.

Abstract

Background: Pregnant and postpartum women in Sub-Saharan Africa are at high risk of HIV acquisition. We evaluated a person-centered dynamic choice intervention for HIV prevention (DCP) among women attending antenatal and postnatal care. Setting: Rural Kenya and Uganda. Methods: Women (aged 15 years or older) at risk of HIV acquisition seen at antenatal and postnatal care clinics were individually randomized to DCP vs. standard of care (SEARCH; NCT04810650). The DCP intervention included structured client choice of product (daily oral pre-exposure prophylaxis or postexposure prophylaxis), service location (clinic or out of facility), and HIV testing modality (self-test or provider-administered), with option to switch over time and person-centered care (phone access to clinician, structured barrier assessment and counseling, and provider training). The primary outcome was biomedical prevention coverage—proportion of 48-week follow-up with self-reported pre-exposure prophylaxis or postexposure prophylaxis use, compared between arms using targeted maximum likelihood estimation. Results: Between April and July 2021, we enrolled 400 women (203 intervention and 197 control); 38% were pregnant, 52% were aged 15–24 years, and 94% reported no pre-exposure prophylaxis or postexposure prophylaxis use for ≥6 months before baseline. Among 384/400 participants (96%) with outcome ascertained, DCP increased biomedical prevention coverage 40% (95% CI: 34% to 47%; P < 0.001); the coverage was 70% in intervention vs. 29% in control. DCP also increased coverage during months at risk of HIV (81% in intervention, 43% in control; 38% absolute increase; 95% CI: 31% to 45%; P < 0.001). Conclusion: A person-centered dynamic choice intervention that provided flexibility in product, testing, and service location more than doubled biomedical HIV prevention coverage in a high-risk population already routinely offered access to biomedical prevention options.

Funder

Division of Intramural Research, National Institute of Allergy and Infectious Diseases

Publisher

Ovid Technologies (Wolters Kluwer Health)

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