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Last Updated: 16/12/2022
Personal protection packages for reducing residual malaria transmission in forest-going MMPs in the Greater Mekong Subregion (GMS)
Objectives
To optimize coverage of vector control measures among MMP and reduce residual malaria transmission in the GMS by a two stepped-wedge cluster randomized trials of personal protection packages.
Health Poverty Action (HPA), United Kingdom
National Malaria Control Programme (NMCP) Myanmar, Myanmar
National Institute of Malaria, Parasitology and Entomology (NIMPE) Vietnam, Vietnam
Centre for Malaria Parasitology and Entomology (CMPE), Lao PDR
National Center for Parasitology, Entomology and Malaria Control (CNM) Cambodia, Cambodia
Over the last decade, the burden of malaria has fallen dramatically in the Greater Mekong Subregion, with deaths falling by 95% and cases by 76% between 2012 and 2019.The declining malaria burden in GMS has largely been attributed to the deployment of interventions of malaria prevention tools such as long-lasting Insecticidal Nets (LLIN), and widespread availability of rapid diagnostic tests and artemisinin combination therapies. However, residual transmission exists among high risk populations, particularly mobile and migrant populations who enter forests for work. New interventions targetting these high risk groups are needed if countries of the Greater Mekong Subregion are to achieve malaria elimination by 2030.
The personal protection package includes WHO prequalified long-lasting insecticidal net (LLIN), insect repellent (N, N-Diethyl-meta-toluamide (DEET), insecticide-treated clothes (ITC), and a MMP-tailored behavioural change communication (BCC) package. The study design is a stepped-wedge cluster-randomized controlled trial with nested mixed methods study. The stepped-wedge cluster randomized trial will estimate the effectiveness of a personal protection package provided to forest-going MMPs (the intervention) delivered by village malaria volunteers at the site (village/worksite) level on reducing Plasmodium spp. infections (primary outcome). Whilst the personal protection package will be provided to mobile and migrant populations in each village in a step-wise manner, primary and secondary outcomes relating to malaria testing will be collected in all consenting individuals in the village who present for malaria rapid diagnostic tests, whether they are mobile and migrant people or not. The study will also include investigation of antibody responses to Plasmodium spp. and mosquito vectors and molecular markers of antimalarial drug resistance.
Jan 2021 — Dec 2022