Logo Lanfrica
  • Home
  • Atlas
  • Insights
  • Docs
  • Sign in

© 2026 Lanfrica. All rights reserved. All copyrights of the resources shown on the Lanfrica website belong to the original copyright holders, unless explicitly stated otherwise.

Requirements for designing cluster randomised control trials to detect suppression of malaria vector population densities

Domain:

healthcare

Record type:

paper
Creator:
Hancock, Penelope A.HuiEpoMil
Publisher:
fig
Host:avatar
Abstract Background Novel interventions for mosquito-borne disease control which release modified mosquitoes that are sterilised or genetically modified to cause offspring inviability are progressing towards field applications. Cluster randomised control trials (CRCTs) could provide robust assessment of intervention efficacy in suppressing mosquito populations in field environments, but guidance on designing CRCTs to detect mosquito suppression impacts is limited. Results We developed statistical models to simulate CRCTs, informed by a 5-year time series measuring densities of malaria vector species from the Anopheles gambiae complex in four villages in western Burkina Faso. We estimated requirements for parallel and step wedge designs, varying the targeted vector species, the suppression effect and the monitoring regime. For a suppression effect of 50%, 21–22 clusters were required to detect suppression with 90% power when all An. gambiae complex species were targeted, while 24–26 clusters were required when only An. coluzzii was targeted and 60–66 clusters were required when only An. gambiae was targeted. For stronger suppression effects, required trial sizes depended less on target species, with 9–10 clusters being sufficient to detect a 90% suppression effect. We investigated how reducing sampling effort, by sampling fewer houses and restricting sampling to rainy season months, affected statistical power. Conclusions Our results provide empirically based guidance for designing CRCTs to evaluate interventions aiming to suppress malaria vector populations.

Visit

doi.orgspringernature.figshare.com

Tags

MedicineMolecular BiologyBiotechnologyEcologyFOS: Biological sciencesBiological Sciences not elsewhere classifiedMathematical Sciences not elsewhere classifiedScience PolicyInfectious DiseasesFOS: Health sciences

Licenses

Creative Commons Attribution 4.0 Internationalhttps://creativecommons.org/licenses/by/4.0/legalcode

Similar

A systematic review of entomological outcomes and sampling approaches used in the evaluation of cluster randomised controlled trials for malaria vector control productsAccounting for complex intracluster correlations in longitudinal cluster randomized trials: a case study in malaria vector controlMonitoring of Larval Habitats and Mosquito Densities in the Sudan Savanna of Mali: Implications for Malaria Vector ControlSystematic identification of plausible pathways to potential harm via problem formulation for investigational releases of a population suppression gene drive to control the human malaria vector Anopheles gambiae in West AfricaPharmacometric analyses of various ivermectin dose regimens in Kenya to inform dosing in mass drug administration trials for malaria vector control.Intraclass Correlation Coefficients for Designing Cluster-Randomized Trials in Sub-Saharan Africa Education

A systematic review of entomological outcomes and sampling approaches used in the evaluation of cluster randomised controlled trials for malaria vector control products

Abstract Background Entomological outcomes are critical for understanding the biological mechanisms

Accounting for complex intracluster correlations in longitudinal cluster randomized trials: a case study in malaria vector control

Abstract Background The effectiveness of malaria vector control interventions is often evaluated usi

Monitoring of Larval Habitats and Mosquito Densities in the Sudan Savanna of Mali: Implications for Malaria Vector Control

In Mali, anopheline mosquito populations increase sharply during the rainy season, but are barely de

Systematic identification of plausible pathways to potential harm via problem formulation for investigational releases of a population suppression gene drive to control the human malaria vector Anopheles gambiae in West Africa

Abstract Background Population suppression gene drive has been

Pharmacometric analyses of various ivermectin dose regimens in Kenya to inform dosing in mass drug administration trials for malaria vector control.

Objectives A promising strategy in malaria prevention is vector control through mass drug administra

Intraclass Correlation Coefficients for Designing Cluster-Randomized Trials in Sub-Saharan Africa Education

Objective: Over the past two decades, the lack of reliable empirical evidence