The combination of a high faecal-related disease burden and inadequate infrastructure suggests that investment in expanding sanitation access in densely populated urban slums can yield important public health gains. No rigorous, controlled intervention studies have evaluated the health effects of decentralised (non-piped) sanitation in an informal urban setting, despite the role that such technologies will likely play in scaling up access.
Methods. We have designed a controlled, before-and-after (CBA) trial to estimate the health impacts of an urban sanitation intervention in informal neighbourhoods of Maputo, Mozambique, including an assessment of whether exposures and health outcomes vary by localised population density. The intervention consists of private pour-flush latrines (to septic tank) shared by multiple households in compounds or household clusters. We will measure objective health outcomes in approximately 1100 children (550 children with household access to interventions, 550 matched controls using existing shared private latrines in poor sanitary conditions), at 2 time points: immediately before the intervention and at follow-up after 12 months of latrine use.
Primary outcome. We define our primary outcome as combined prevalence of the following enteric infections in stool samples from children: Campylobacter; Clostridium difficile, Toxin A/B; Es. coli O157; ETEC LT/ST; Shiga-like toxin producing Es. coli (STEC) stx1/stx2; Salmonella; Shigella; V. cholerae; Yersinia enterocolitica; Giardia; Cryptosporidium; and Entamoeba histolytica. These and other enteric infections are increasingly thought to be related to environmental enteric dysfunction (EED) and stunting. Additionally, we will detect viral pathogens adenovirus 40/41, Norovirus GI/GII, and Rotavirus A, though we have excluded viral infections from the primary outcome definition.
Secondary outcome measures include soil-transmitted helminth (STH) reinfection (A. lumbricoides, T. trichiura, and hookworm by Kato-Katz and qPCR) in children following baseline deworming and prevalence of reported diarrhoeal disease (7-day recall). Tertiary outcomes include biomarkers for EED including neopterin, α-antitrypsin, and myeloperoxidase in stools; anthropometric measures to compute height-for-age Z-scores and other measures of growth in children; and salivary IGF-1.
Behaviour changeHealth and hygieneSpecific to one or several countriesOtherBill & Melinda Gates FoundationUrban informal settlements (slums)University, education or research institution
Mozambique
Project location