Evidence map›Paper›PMID 41857747›Full record

ArticleTrials2026

A diffusion model for mosquito control trials with spillover: application to calculations of power, sample size, and bias.

Thomas A Smith, Luzia N Felber, Neal A Alexander, Pélagie E B Aboa, Claver N Adjobi, Julien Z B Zahouli, Pie Müller

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In one paragraph

Article in Trials, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Thomas A SmithSwiss Tropical and Public Health Institute, Kreuzstrasse 2, Allschwil, 4123, Switzerland. Thomas-A.Smith@unibas.ch.
Luzia N FelberSwiss Tropical and Public Health Institute, Kreuzstrasse 2, Allschwil, 4123, Switzerland.
Neal A AlexanderMRC International Statistics and Epidemiology Group, London School of Hygiene and Tropical Medicine, London, UK.
Pélagie E B AboaSwiss Tropical and Public Health Institute, Kreuzstrasse 2, Allschwil, 4123, Switzerland.
Claver N AdjobiCentre Suisse de Recherches Scientifiques en Côte d'Ivoire, Abidjan, Côte d'Ivoire.
Julien Z B ZahouliCentre d'Entomologie Médicale Et Vétérinaire de L'Université Alassane Ouattara, Bouaké, Côte d'Ivoire.
Pie MüllerSwiss Tropical and Public Health Institute, Kreuzstrasse 2, Allschwil, 4123, Switzerland.

Funding

Bill and Melinda Gates Foundation INV025569
6 · The paper itself

Abstract

backgroundMosquito movement is ubiquitous and complicates the design of cluster randomized trials (CRTs) of vector control interventions because it can cause spillover between trial arms. There has been no analytical approach to quantify the impact of this spillover on trial power, required sample sizes, or bias. This precludes formal allowance for spillover in formulae for study power, and a precautionary principle is generally used in trial design, leading to CRTs with very large clusters and extensive buffer zones between arms.

methodsThe diffusion equation was solved to give a mathematical model for mosquito displacement in a cluster randomized trial. This provides an explicit function for calculating the bias in efficacy estimates due to mosquito movement. Substituting this into a conventional formula for the power gives adjusted sample size and power estimates and indicates how the exclusion of data from buffer zones affects bias and power. The method is generally applicable to trials with entomological outcomes, or to malaria trials with epidemiological outcomes, providing these can be related to biting densities of mosquitoes. It is illustrated with the baseline data from an intervention trial against Aedes aegypti in Côte d'Ivoire.

resultsDespite the small size of the Côte d'Ivoire trial, it has adequate power to detect true intervention efficacy of ≥0.4, even in the presence of considerable spillover. If the spillover extends over a wide distance, the power will be considerably increased by using buffer zones.

conclusionsThe analytical approach can be incorporated into power calculations for CRTs with geographical spillover, whenever the diffusion model is considered an acceptable approximation. The example suggests that the key to obtaining adequate power in the presence of spillover is the inclusion of a sufficiently large number of clusters, even if only a small amount of data can be obtained from each cluster. The method can be implemented in a publicly available R package.

Indexed as

AedesMalariaModels, BiologicalMosquito ControlMosquito VectorsRandomized Controlled Trials as TopicResearch DesignAnimalsBiasCote d'IvoireHumansSample SizeAedesAnophelesClusterDiffusionMosquitoMovementPower bias

Identifiers

PMID41857747
PMCPMC13123211

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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.