Adaptive intervention strategies for malaria vector control in western Kenya: a cluster, sequential, multiple-assignment, randomised, open-label trial

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Authors: Guofa Zhou, Xiaoming Wang, Ming‐Chieh Lee, Maxwell Gesuge Machani, Kelley M. Kidwell, Harrysone Atieli, James W. Kazura, John I Githure, Daibin Zhong, Guiyun Yan
Cited by: 1
References: 23

Abstract

BACKGROUND: Many regions in Africa continue to experience a high malaria burden, highlighting the need for improved intervention tools adapted to local eco-epidemiological contexts. The aims of this study were to develop and evaluate adaptive intervention strategies for malaria vector control tailored to these local conditions. METHODS: and all residents in the clusters were invited to participate in the study. In stage 1, clusters were randomly assigned, in a 1:1:1 ratio, to standard pyrethroid-based long-lasting insecticidal nets (LLINs; henceforth standard LLINs) alone, piperonyl butoxide-treated LLINs (henceforth PBO nets), or standard LLINs plus annual indoor residual spraying (IRS), stratified by subcounty. Due to the nature of the interventions, masking to intervention was not feasible. Clusters with an adjusted incidence rate ratio (aIRR) of 0·8 or more were classified as non-responders. Non-responding clusters were re-randomised in stage 2. The non-responding clusters from the stage 1 PBO nets group were re-randomised, in a 1:1 ratio, to receive either supplemental microbial larviciding or annual IRS. The non-responding clusters from the stage 1 standard LLINs plus annual IRS group were re-randomised, in a 1:1 ratio, to either IRS twice per year (henceforth biannual IRS), or enhanced IRS annually, which included spraying both indoor residential structures and peridomestic resting structures not covered by routine IRS. The coprimary outcomes were clinical malaria incidence at 1-6 months, 7-12 months, and 13-18 months post-intervention, assessed through active surveillance of cohort populations once every 2 weeks and analysed in all participants with available data. Although the study procedures posed minimal risk to participants, adverse event data were regularly reviewed. The trial was registered with ClinicalTrials.gov (NCT04182126) and is complete. FINDINGS: Between March 8, 2021, and Aug 31, 2024, the study enrolled 47 614 participants (51·8% male, 48·2% female) from 14 246 households in 84 clusters. In stage 1, PBO nets significantly reduced malaria incidence at 1-6 months post-intervention (aIRR 0·75, 95% CI 0·69-0·81; p

Fields of Study & Subjects

Malaria Research and Control Mosquito-borne diseases and control Genetics Bioinformatics and Biomedical Research

Publication details

Journal / source
The Lancet Global Health
Publisher
Elsevier BV
Volume
14
Issue
7
Pages
103939–103939
Publication date
24 April 2026
Language
EN