Evidence map›Paper›PMID 40875480›Full record

Trial reportJournal of acquired immune deficiency syndromes (1999)2025

Higher Acceptability of the Monthly Dapivirine Ring Versus Daily Oral Pre-Exposure Prophylaxis Among Adolescent Girls and Young Women in Sub-Saharan Africa in the REACH Trial.

Barbara A Friedland, Erica N Browne, Sarah T Roberts, Kenneth Ngure, Rita Nakalega, Pippa Macdonald, Cynthia Nombeko Mpongo, Siyanda Tenza, Nomsa Mhlanga, Danny Szydlo and 7 more

Abstract readClinical Trial, Phase IIComparative StudyMulticenter Study
In one paragraph

Trial report in Journal of acquired immune deficiency syndromes (1999), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Barbara A FriedlandPopulation Council, Center for Biomedical Research, New York, NY.ORCID 0000-0002-5041-3634
Erica N BrowneRTI International San Francisco Office, Women's Global Health Imperative (WGHI) Program, San Francisco, CA.
Sarah T RobertsRTI International San Francisco Office, Women's Global Health Imperative (WGHI) Program, San Francisco, CA.
Kenneth NgureJomo Kenyatta University of Agriculture and Technology, School of Public Health, Nairobi, Kenya.
Rita NakalegaMakerere University-John Hopkins University Research Collaboration, Kampala, Uganda.
Pippa MacdonaldUniversity of Cape Town Desmond Tutu HIV Centre, Cape Town, South Africa.
Cynthia Nombeko MpongoUniversity of Cape Town Desmond Tutu HIV Centre, Cape Town, South Africa.
Siyanda TenzaWits Reproductive Health and HIV Institute, Faculty of Health Sciences, Johannesburg, South Africa.
Nomsa MhlangaUniversity of Zimbabwe Clinical Trials Research Centre, Harare, Zimbabwe.
Danny SzydloFred Hutchinson Cancer Research Center, Vaccine and Infectious Disease Division, Seattle, WA.
Sherri JohnsonFHI 360, Durham, NC.
Tara McClureFHI 360, Durham, NC.
Gonasagrie NairStellenbosch University, Centre for Medical Ethics and Law, Stellenbosch, South Africa.
Connie CelumUniversity of Washington, Global Health, Seattle, WA.
Sharon L HillierUniversity of Pittsburgh School of Medicine, Obstetrics, Gynecology and Reproductive Sciences, Magee Womens Hospital of UPMC, Pittsburgh, PA.
Ariane van der StratenASTRA Consulting, Kensington, CA; and.
MTN-034 REACH clinical trial team

Funding

Microbicide Trials NetworkUM1AI068633 · NIAID · MAGEE-WOMEN'S RES INST AND FOUNDATION · PI HILLIER, SHARON L. · 2011 to 2021
$175.0M
UZ-UCSF CTUUM1AI069436 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ZVAVAHERA MIKE CHIRENJE, LYNDA STRANIX-CHIBANDA · 2012 to 2026
$75.9M
Statistical and Data Management Center (SDMC): Microbicide Trials NetworkUM1AI068615 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI BROWN, ELIZABETH RENATA · 2011 to 2021
$66.5M
UZ-UCSF Clinical Trials UnitU01AI069436 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CHIRENJE, ZVAVAHERA MIKE · 2007 to 2011
$49.3M
Laboratory Center (LC): Microbicide Trials NetworkUM1AI106707 · NIAID · MAGEE-WOMEN'S RES INST AND FOUNDATION · PI MELLORS, JOHN W, ROHAN, LISA CENCIA · 2014 to 2021
$27.1M
Division of Intramural Research, National Institute of Allergy and Infectious Diseases UM1AI068615Division of Intramural Research, National Institute of Allergy and Infectious Diseases UM1AI068633Division of Intramural Research, National Institute of Allergy and Infectious Diseases UM1AI106707NIAID NIH HHS U01 AI069436NIAID NIH HHS UM1 AI068615NIAID NIH HHS UM1 AI068633NIAID NIH HHS UM1 AI069436NIAID NIH HHS UM1 AI106707
6 · The paper itself

Abstract

backgroundOral pre-exposure prophylaxis (PrEP) is effective for HIV prevention , yet use has been inconsistent in adolescent girls and young women (AGYW). We compared PrEP with the dapivirine vaginal ring (ring) among AGYW in MTN-034 (REACH).

methodsWe randomized 247 16-21-yr-old AGYW (South Africa, Uganda, Zimbabwe) to the sequence of using the ring and oral PrEP for 6 m each (February 2019-September 2021). Participants rated overall product acceptability (1, dislike very much to 5, like very much) after 3 m and 6 m, and product characteristics/use attributes after 3 m. We compared proportions of participants rating each product a "5" (binomial model with generalized estimating equations). We assessed associations between product characteristics/use attribute ratings at 3 m and overall acceptability after 6 m (χ 2 ). RESULTSOVERALL,: 65% and 41% of participants rated the ring versus PrEP a "5" (adjusted risk difference [aRD] 24%, 95% CI: 15%, 32%; P < 0.001). For both products, high overall acceptability was associated with "excellent" self-rated adherence (ring, P < 0.001; PrEP, P = 0.03), product appearance (ring, P = 0.005; PrEP, P < 0.001), and ease of use (ring, P = 0.001; PrEP, P = 0.003). Not worrying about/or experiencing side effects were also associated with high acceptability of oral PREP.

conclusionsThe dapivirine ring was highly acceptable to substantially more individuals than oral PrEP, although a significant minority rated oral PrEP highly, even after using the ring. As has been found in the contraceptive field, offering AGYW a choice of PrEP products is likely to increase the use of any HIV prevention method in this vulnerable population.

Indexed as

Anti-HIV AgentsHIV InfectionsPatient Acceptance of Health CarePre-Exposure ProphylaxisPyrimidinesAdministration, IntravaginalAdministration, OralAdolescentAfrica South of the SaharaContraceptive Devices, FemaleDelayed-Action PreparationsFemaleHumansUgandaYoung AdultZimbabweAnti-HIV AgentsDapivirineDelayed-Action PreparationsPyrimidinesacceptabilityadolescent girls and young womenAfrica < Regiondapivirine ringHIV preventionPrEP

Identifiers

PMID40875480
PMCPMC12599507

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.