Sangoro 2014a.

Study characteristics
Methods	cRCT Unit of randomization: cluster of households ICC: not reported Trial duration: 14 months
Participants	Adults or children living in malaria endemic regions Non‐high risk population
Interventions	Topical repellent: 15% DEET lotion Controls: placebo lotion Co‐interventions: LLINs Treatment arms: ‐ Intervention: 10 clusters, 468 households and 2224 participants ‐ Controls: 10 clusters, 469 households and 2202 participants
Outcomes	‐ Malaria case incidence: new cases of clinical malaria (caused by Plasmodium spp.) confirmed through blood smears or RDTs ‐ Adherence to regular usage of the intervention (defined based on recommendations provided by researchers to participants of individual trials)
Notes	Carried out in Tanzania. Funded by Population Services International.