Recipient organisationCheikh Anta Diop University of Dakar
Funding£1.3M
PeriodJul 2012 — Sept 2015
In plain English
AI plain-English summary
Malaria persists in hidden pockets of transmission even after mass bednet distribution, and this trial will test whether saturating those villages with insecticide and drugs can stamp out the remaining infections. The problem is that standard malaria control—bednets and basic treatment—has driven cases down sharply in parts of Africa, but transmission continues in small clusters. These foci re-seed infections into surrounding communities. If immunity wanes in a population that has seen few cases for years, a resurgence could be devastating. The trial in central Senegal will identify high-transmission villages from the previous year’s case data, then hit them with indoor residual spraying just before the rainy season and mass drug administration (artemisinin plus piperaquine) in September and October. It will also compare treating everyone in the village versus screening and treating only those who test positive. If the approach works, it could provide a practical, spatially targeted playbook for pushing malaria toward elimination in regions where it once killed large numbers of children. The findings would inform national control programmes across Africa, potentially shifting strategy from blanket coverage to precision elimination of residual transmission.
View original technical description
There has recently been a sharp decline in the incidence of malaria in several parts of Africa, due to the strengthening of control measures, most importantly the large-scale distribution of free and highly subsidized insecticide-treated bednets, raising the prospect that malaria could be eliminated. But despite scaling-up of control, transmission persists in foci which provide a continuing source of infection. Additional strategies are needed to eliminate these foci, this is important because a resurgence of malaria in populations whose acquired immunity has lapsed could have a devastating impact. The aim of this study is to find out whether we can virtually eliminate malaria in a population by delivering intensified control in villages with persistent transmission. The trial, which will take place in central Senegal, will run over two years. Each year we will select villages to be targeted, on the basis of malaria cases reported in the previous year, and we will operate intensified malaria control in these villages, attacking the vector population with indoor residual spraying with a highly effective residual insecticide, and treating infected persons with effective antimalarial drugs to remove the reservoir of infection. The hope is that by targeting the places which favour transmission, there will be reduction in the prevalence of malaria infection not only in areas which are targeted but also in the surrounding villages that are not targeted. Spraying is done just before the rainy season begins, coating the places where the first mosquitoes to emerge will rest, to kill them before they can transmit infection. Chemotherapy will be done once early in September, to clear the reservoir of infection in humans before the height of the transmission season, and again in October to clear any persisting or new infections. We will use a combination of two drugs, an artemisinin to quickly clear malaria infection, and piperaquine, which provides prophylaxis for about a month. Treatment of carriers is known to be an essential component of elimination programmes but it is an open question whether it is better to administer antimalarial drugs to all members of the community or screen and treat only those who are positive. The trial will use both approaches to see which is most effective and practical. It is hoped that the findings of this study will contribute to the elimination of malaria in areas where until recently it was the major cause of child deaths.
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