Malaria
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: The study population will consist of residents of the locations and households targeted by the intervention demonstration experiments. We will select 12 locations that are malaria hotspots. Locations within a district will be at least 10 km apart and that are malaria hotspot areas. Larval habitat mapping, larval surveys and larviciding (where applicable) will be done in a radius of 1 km around each location. A study location should include at least 50 homesteads.
Exclusion criteria
Exclusion criteria: Locations that are not malaria hotspot areas
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary entomological objective is to assess whether winter larviciding combined with IRS prior to the rainy season reduce vector adult density inside and outside houses when compared with areas where only IRS is implemented. ;The primary clinical objective is to assess whether winter larviciding combined with IRS prior to the rainy season provides added protection against clinical malaria when compared with areas that receive IRS alone. | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary entomological objectives include (1) to determine whether the combined intervention reduces the proportion of aquatic habitats containing Anopheles larvae not only during the intervention but also when larviciding is not implemented (spill-over effect, synergistic effect with IRS); (2) the Anopheles larval density in selected habitats; and (3) the entomological inoculation rate. ;The secondary clinical objective is to determine if the combined intervention reduces the rate of parasite infection and parasite density | — |
Countries
Botswana, Namibia, Swaziland
Contacts
Post doctoral research fellow