While cluster randomised clinical trials (CRTs) are the gold standard to determine the efficacy of novel public health interventions, these trials are generally very expensive and take many years from inception to final results. As a consequence, few of these trials are done. For PvSeroTAT a single large cluster randomised trial is being conducted. However, these are an increasing number of pilot implementation and scale-up studies being conducted in several countries. This PhD will develop and apply statistical and mathematical models to estimate the impact of PvSeroTAT and other malaria control interventions on malaria burden from both CRTs and non-CRT PvSeroTAT studies and extrapolate these results to other settings and PvSeroTAT implementation modes.
The aim of the PhD project is to assist in the development and validation of P. vivax sero-diagnostic tests across diverse transmission settings, evaluate pilot and scale-up studies to quantify epidemiological impact, and contribute to frameworks that enable national malaria programs and other parties to integrate PvSeroTaT into elimination strategies. The PhD student will work as part of the Vivax Serology Partnership (VISPA) consortium: Expanding Access to Vivax Serology Diagnostics), which is across multiple institutes within Australia, Europe and throughout vivax endemic areas in the Asia-Pacific, Africa and Latin America.