Impact of financial incentives on viral suppression among adults initiating HIV treatment in Tanzania: a hybrid effectiveness-implementation trial.


Journal

The lancet. HIV
ISSN: 2352-3018
Titre abrégé: Lancet HIV
Pays: Netherlands
ID NLM: 101645355

Informations de publication

Date de publication:
01 Aug 2024
Historique:
received: 14 12 2023
revised: 22 05 2024
accepted: 23 05 2024
medline: 5 8 2024
pubmed: 5 8 2024
entrez: 4 8 2024
Statut: aheadofprint

Résumé

Small incentives could improve engagement in HIV care. We evaluated the short-term and longer-term effects of financial incentives for visit attendance on viral suppression among adults initiating antiretroviral therapy (ART) in Tanzania. In a type 1 hybrid effectiveness-implementation study, we randomised (1:1) 32 primary care HIV clinics in four Tanzanian regions to usual care (control group) or the intervention (usual care plus ≤6 monthly incentives [22 500 Tanzanian Shillings, about US$10, each], conditional on visit attendance). Adults (aged ≥18 years) initiating ART (<30 days) who owned a mobile phone and had no plans to transfer to another facility were eligible. The primary outcome was retention on ART with viral suppression (<1000 copies per mL) at 12 months. Secondary outcomes included retention on ART with viral suppression at 6 months and viral suppression at 6 months and 12 months using a lower threshold (<50 copies per mL). Intent-to-treat analysis and a cluster-based permutation test were used to evaluate the effect of financial incentives on outcomes. This trial is registered with ClinicalTrials.gov, NCT04201353, and is completed. Between May 28, 2021, and March 8, 2022, 1990 participants (805 male and 1185 female) were enrolled in the study. 1059 participants were assigned to the intervention group and 931 participants were assigned to the control group. Overall, 1536 (88%) participants at 6 months and 1575 (83%) at 12 months were on ART with viral suppression. At 12 months, 6 months after the intervention ended, 866 (85%) participants in the intervention group compared with 709 (81%) in the control group had viral loads less than 1000 copies per mL (adjusted risk difference [aRD] 4·4 percentage points, 95% CI -1·4 to 10·1, permutation test p=0·35). At 6 months, 858 participants (90%) in the intervention group were on ART with viral loads less than 1000 copies per mL compared with 678 (86%) in the control group (aRD 5·1 percentage points, 95% CI 1·1 to 9·1, permutation test p=0·06). Effects were larger at 6 months and 12 months with the lower threshold for viral suppression, and there was significant effect heterogeneity by region. Adverse events included 106 deaths (56 in the control group and 50 in the intervention group), none related to study participation. Short-term incentives for visit attendance had modest, short term benefits on viral suppression and did not harm retention or viral suppression after discontinuation. These findings suggest the need to understand subgroups who would most benefit from incentives to support HIV care. National Institute of Mental Health. For the Swahili translation of the abstract see Supplementary Materials section.

Sections du résumé

BACKGROUND BACKGROUND
Small incentives could improve engagement in HIV care. We evaluated the short-term and longer-term effects of financial incentives for visit attendance on viral suppression among adults initiating antiretroviral therapy (ART) in Tanzania.
METHODS METHODS
In a type 1 hybrid effectiveness-implementation study, we randomised (1:1) 32 primary care HIV clinics in four Tanzanian regions to usual care (control group) or the intervention (usual care plus ≤6 monthly incentives [22 500 Tanzanian Shillings, about US$10, each], conditional on visit attendance). Adults (aged ≥18 years) initiating ART (<30 days) who owned a mobile phone and had no plans to transfer to another facility were eligible. The primary outcome was retention on ART with viral suppression (<1000 copies per mL) at 12 months. Secondary outcomes included retention on ART with viral suppression at 6 months and viral suppression at 6 months and 12 months using a lower threshold (<50 copies per mL). Intent-to-treat analysis and a cluster-based permutation test were used to evaluate the effect of financial incentives on outcomes. This trial is registered with ClinicalTrials.gov, NCT04201353, and is completed.
FINDINGS RESULTS
Between May 28, 2021, and March 8, 2022, 1990 participants (805 male and 1185 female) were enrolled in the study. 1059 participants were assigned to the intervention group and 931 participants were assigned to the control group. Overall, 1536 (88%) participants at 6 months and 1575 (83%) at 12 months were on ART with viral suppression. At 12 months, 6 months after the intervention ended, 866 (85%) participants in the intervention group compared with 709 (81%) in the control group had viral loads less than 1000 copies per mL (adjusted risk difference [aRD] 4·4 percentage points, 95% CI -1·4 to 10·1, permutation test p=0·35). At 6 months, 858 participants (90%) in the intervention group were on ART with viral loads less than 1000 copies per mL compared with 678 (86%) in the control group (aRD 5·1 percentage points, 95% CI 1·1 to 9·1, permutation test p=0·06). Effects were larger at 6 months and 12 months with the lower threshold for viral suppression, and there was significant effect heterogeneity by region. Adverse events included 106 deaths (56 in the control group and 50 in the intervention group), none related to study participation.
INTERPRETATION CONCLUSIONS
Short-term incentives for visit attendance had modest, short term benefits on viral suppression and did not harm retention or viral suppression after discontinuation. These findings suggest the need to understand subgroups who would most benefit from incentives to support HIV care.
FUNDING BACKGROUND
National Institute of Mental Health.
TRANSLATION UNASSIGNED
For the Swahili translation of the abstract see Supplementary Materials section.

Identifiants

pubmed: 39098325
pii: S2352-3018(24)00149-8
doi: 10.1016/S2352-3018(24)00149-8
pii:
doi:

Banques de données

ClinicalTrials.gov
['NCT04201353']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license. Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests We declare no competing interests.

Auteurs

Prosper F Njau (PF)

National AIDS, STIs and Hepatitis Control Programme, Ministry of Health, Dodoma, Tanzania.

Emmanuel Katabaro (E)

Health for a Prosperous Nation, Dar es Salaam, Tanzania.

Solis Winters (S)

School of Public Health, University of California, Berkeley, CA, USA.

Amon Sabasaba (A)

Health for a Prosperous Nation, Dar es Salaam, Tanzania.

Kassim Hassan (K)

Health for a Prosperous Nation, Dar es Salaam, Tanzania.

Babuu Joseph (B)

Health for a Prosperous Nation, Dar es Salaam, Tanzania.

Hamza Maila (H)

Health for a Prosperous Nation, Dar es Salaam, Tanzania.

Janeth Msasa (J)

Health for a Prosperous Nation, Dar es Salaam, Tanzania.

Carolyn A Fahey (CA)

School of Public Health, University of California, Berkeley, CA, USA; School of Public Health, University of Washington, Seattle, WA, USA.

Laura Packel (L)

School of Public Health, University of California, Berkeley, CA, USA.

William H Dow (WH)

School of Public Health, University of California, Berkeley, CA, USA.

Nicholas P Jewell (NP)

School of Public Health, University of California, Berkeley, CA, USA; London School of Hygiene & Tropical Medicine, London, UK.

Nzovu Ulenga (N)

Management and Development for Health, Dar es Salaam, Tanzania.

Natalino Mwenda (N)

Rasello, Dar es Salaam, Tanzania.

Sandra I McCoy (SI)

School of Public Health, University of California, Berkeley, CA, USA. Electronic address: smccoy@berkeley.edu.

Classifications MeSH