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Study protocol for a cluster randomised controlled factorial design trial to assess the effectiveness and feasibility of reactive focal mass drug administration and vector control to reduce malaria transmission in the low endemic setting of Namibia.

  • Author(s): Medzihradsky, Oliver F;
  • Kleinschmidt, Immo;
  • Mumbengegwi, Davis;
  • Roberts, Kathryn W;
  • McCreesh, Patrick;
  • Dufour, Mi-Suk Kang;
  • Uusiku, Petrina;
  • Katokele, Stark;
  • Bennett, Adam;
  • Smith, Jennifer;
  • Sturrock, Hugh;
  • Prach, Lisa M;
  • Ntuku, Henry;
  • Tambo, Munyaradzi;
  • Didier, Bradley;
  • Greenhouse, Bryan;
  • Gani, Zaahira;
  • Aerts, Ann;
  • Gosling, Roly;
  • Hsiang, Michelle S
  • et al.


To interrupt malaria transmission, strategies must target the parasite reservoir in both humans and mosquitos. Testing of community members linked to an index case, termed reactive case detection (RACD), is commonly implemented in low transmission areas, though its impact may be limited by the sensitivity of current diagnostics. Indoor residual spraying (IRS) before malaria season is a cornerstone of vector control efforts. Despite their implementation in Namibia, a country approaching elimination, these methods have been met with recent plateaus in transmission reduction. This study evaluates the effectiveness and feasibility of two new targeted strategies, reactive focal mass drug administration (rfMDA) and reactive focal vector control (RAVC) in Namibia.

Methods and analysis

This is an open-label cluster randomised controlled trial with 2×2 factorial design. The interventions include: rfMDA (presumptive treatment with artemether-lumefantrine (AL)) versus RACD (rapid diagnostic testing and treatment using AL) and RAVC (IRS with Acellic 300CS) versus no RAVC. Factorial design also enables comparison of the combined rfMDA+RAVC intervention to RACD. Participants living in 56 enumeration areas will be randomised to one of four arms: rfMDA, rfMDA+RAVC, RACD or RACD+RAVC. These interventions, triggered by index cases detected at health facilities, will be targeted to individuals residing within 500 m of an index. The primary outcome is cumulative incidence of locally acquired malaria detected at health facilities over 1 year. Secondary outcomes include seroprevalence, infection prevalence, intervention coverage, safety, acceptability, adherence, cost and cost-effectiveness.

Ethics and dissemination

Findings will be reported on, in peer-reviewed publications and through stakeholder meetings with MoHSS and community leaders in Namibia.

Trial registration number

NCT02610400; Pre-results.

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