Journal
MALARIA JOURNAL
Volume 20, Issue 1, Pages -Publisher
BMC
DOI: 10.1186/s12936-021-03924-7
Keywords
Stepped wedge cluster randomized trial; Contamination; Sigmoid random effects model; Contamination range; Effective coverage; Malaria
Categories
Funding
- Swiss National Science Foundation [310030_162837]
- COmON Foundation (University Fund Wageningen)
- EU Seventh Framework Programme (FP7/2007-2013) [265660]
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The analysis extends from CRTs to SWCRTs, providing estimates of effectiveness based on intervention coverage. Results show that the contamination range in malaria intervention trials is much smaller than the distance Anopheles mosquitoes can fly. An appropriate analysis can eliminate the need for buffer zones in trials, making them more cost-efficient.
Background: In cluster randomized trials (CRTs) or stepped wedge cluster randomized trials (SWCRTs) of malaria interventions, mosquito movement leads to contamination between trial arms unless buffer zones separate the clusters. Contamination can be accounted for in the analysis, yielding an estimate of the contamination range, the distance over which contamination measurably biases the effectiveness. Methods: A previously described analysis for CRTs is extended to SWCRTs and estimates of effectiveness are provided as a function of intervention coverage. The methods are applied to two SWCRTs of malaria interventions, the SolarMal trial on the impact of mass trapping of mosquitoes with odor-baited traps and the AvecNet trial on the effect of adding pyriproxyfen to long-lasting insecticidal nets. Results: For the SolarMal trial, the contamination range was estimated to be 146 m (95% credible interval [0.052, 0.923] km), together with a 31.9% (95% credible interval [15.3, 45.8]%) reduction of Plasmodium infection, compared to the 30.0% reduction estimated without accounting for contamination. The estimated effectiveness had an approximately linear relationship with coverage. For the AvecNet trial, estimated contamination effects were minimal, with insufficient data from the cluster boundary regions to estimate the effectiveness as a function of coverage. Conclusions: The contamination range in these trials of malaria interventions is much less than the distances Anopheles mosquitoes can fly. An appropriate analysis makes buffer zones unnecessary, enabling the design of more cost-efficient trials. Estimation of the contamination range requires information from the cluster boundary regions and trials should be designed to collect this.
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