Last Updated: 28/05/2025
Effectiveness of Seasonal Malaria Chemoprevention in Koulikoro, Mali
Objectives
The overall goal of this project is to improve the effectiveness of Seasonal Malaria Chemoprevention (SMC) and reduce the burden of malaria in Mali. The effectiveness of three different treatment regimens for SMC will be evaluated with respect to implementation, malaria morbidity, cost, protective immunity to malaria and potential emergence of drug resistance with respect to implementation.
Specific objectives of this project are:
- To determine the effectiveness of SMC extended to children up to 10 years old on the incidence and prevalence of malaria over entire district of Koulikoro using a cluster randomized controlled trial study design.
- To assess potential long term effect of SMC on malaria epidemiology (acquisition of protective immunity, parasite population dynamics, drug resistance and transmission).
- To conduct a cost-effectiveness analysis of SMC extended to 5-10 years old as compared with standard protocol of SMC provision to children less than 5 years old with regard to delivery and implementation strategies and financial cost per malaria case averted and per child.
University of Sciences Techniques and Technologies of Bamako (USTTB), Mali
Seasonal malaria chemoprevention (SMC), is a prophylactic antimalarial regimen of sulfadoxine- pyrimethamine (SP) and amodiaquine (AQ) recommended by the World Health Organization (WHO) for pre- venting malaria episodes in children under 5 years of age in specific, highly seasonal, transmission settings. In 2012, the WHO called on all countries in the Sahel sub-region of Africa to implement SMC. The WHO reports that SMC is 75% effective in preventing all malaria episodes and 75% of severe malaria episodes when im- plemented according to its guidelines. From 2013-2016, the West African International Centers of Excellence for Malaria Research (ICEMR) carried out a cohort study including 1,814 subjects in a remote village in Dangassa, Mali. Peak malaria incidence reductions following SMC coverage in children less than 5 years of age were observed in 2015 at 38%, falling far short of the 75% protective efficacy suggested by the WHO. These estimates call into question the effectiveness of SMC implementation or the efficacy of the therapy itself in high malaria transmission in Mali like Dangassa. The purpose of the proposed study is two-fold. First, cross- sectional and cohort studies are used to establish levels of SMC coverage and implementation practices to as- sess effectiveness of SMC. Second, if results suggest operational, implementation, SP or AQ resistance and SMC coverage practices are acceptable, a randomized control trial will be conducted to measure the effective- ness of extending SMC to children up to 10 years of age. Alternatively, if operational and implementation strategies are found to be functioning poorly and drug resistance is found to be at acceptable levels suggesting the potential for efficacy of well implemented SMC, a randomized control trial will be used to assess the effec- tiveness of different delivery systems to achieve the intended effect by improving coverage. The findings from years 1 and 2 implementation studies will serve as the go (conduct high quality efficacy study) versus no-go (conduct further intervention effectiveness studies around operations and implementation strategies) criteria for years 3-5.
- Study Type : Interventional (Clinical Trial)
- Estimated Enrollment : 4556 participants
- Allocation: Randomized
- Intervention Model: Crossover Assignment
- Intervention Model Description: A cluster randomized design
ClinicalTrials.gov Identifier: NCT04149106
NIH Reporter - Project detailsClinicaltrials.gov - Trial details
Apr 2019 — Mar 2020
$458,810


