Field Studies on the Feasibility of Interrupting the Transmission of Soil-transmitted Helminths (STH)

  • STATUS
    Recruiting
  • End date
    Dec 7, 2023
  • participants needed
    380000
  • sponsor
    University of Washington
Updated on 1 March 2022
albendazole
mebendazole
ivermectin
mass drug administration
diethylcarbamazine
Accepts healthy volunteers

Summary

Over 1.5 billion people are infected with soil-transmitted helminths (STH). Global STH guidelines recommend MDA (mass drug administration) of albendazole or mebendazole to targeted populations, including pre-school age children and school-age children. However mathematical models suggests that current MDA strategies are not sufficient for interrupting disease transmission in most areas. Meanwhile many lymphatic filariasis (LF) programs have successfully treated entire populations with albendazole (in combination with ivermectin or diethylcarbamazine) and are transitioning to a state of post-MDA surveillance. This project will conduct a series of community-based cluster randomized trials in India, Malawi, and Benin to determine if maintaining three years of MDA with albendazole to entire communities following the cessation of LF programs can interrupt STH transmission in focal geographic areas. Additionally, this study aims to compare the efficacy of community-wide MDA versus targeted MDA of children in interrupting the transmission of STH. Nested implementation science research will be used to optimize the intervention, identify contextual factors influencing trial efficacy, and evaluate the feasibility of sustaining and scaling community-wide MDA for STH. These data will provide evidence necessary to inform future guidelines, policies, and operational plans as country partners engage in intensified approaches to eliminate these disabling diseases.

Details
Condition Helminthiasis, Filariasis
Treatment Albendazole
Clinical Study IdentifierNCT03014167
SponsorUniversity of Washington
Last Modified on1 March 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

Resident of study clusters
Ages 12 months and older
Willingness of adult aged 18 years and above (or age as per country specific ethical guidelines) or parent/guardian of child to provide written informed consent
Provision of written assent to participate from children aged 8 years and above (or age as per country specific ethical guidelines)

Exclusion Criteria

Less than 12 months of age
Individuals who do not typically reside in the study cluster
Nonconsenting or assenting individuals, as applicable
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