Effectiveness, Feasibility and Acceptability of Seasonal Malaria Chemoprevention in Aweil South County in Northern Bahr Eel Ghazal, South Sudan: A Type 2 Hybrid Effectiveness-implementation Study Using a Convergent Mixed-methods Approach
试验速览
- 阶段
- 3 期
- 状态
- 进行中（未招募）
- 入组人数
- 3,575
- 试验地点
- 1
- 主要终点
- Malaria incidence in study population in intervention county and eligible children in one control county
研究概览
简要总结
This study aims to explore whether SMC is an effective intervention in the context of Northen Bahr el Gazal state, South Sudan. It also aims to assess the protective efficacy of the antimalarials used in SMC in the target population and investigate levels of parasite resistance in the study counties. If successful, this trial should provide the evidence for SMC to be included in malaria programming and policy in South Sudan.
A Type II hybrid effectiveness-implementation study design will be used to evaluate the effects of a clinical intervention on relevant outcomes whilst collecting information on implementation. It is designed to determine feasibility and effectiveness of an innovative intervention, as well as the protective efficacy of the antimalarial drugs used. The study consists of five components: 1) A series of cross-sectional surveys establishing confirmed malaria cases in children; 2) A prospective cohort study to determine the protective efficacy of SPAQ (if SPAQ provides 28 days of protection from infection) and whether drug concentrations and/or resistance influence the duration of protection; 3) A resistance markers study in children 3-59 months in the research county; 4) Modelling the protective effect of SPAQ in South Sudan to determine where SMC could be a suitable malaria prevention strategy in other areas of the country, and 5) A process evaluation to understand feasibility and acceptability of the SMC intervention in South Sudan.
详细描述
This is an implementation research study, using a Type II hybrid effectiveness-implementation study design, to evaluate the effects of a clinical intervention on relevant outcomes whilst collecting information on implementation.
The study uses pragmatic implementation research with the objective of contributing to the development of practical recommendations for health policy, practice and potential scale up. It is designed as an implementation study to determine effectiveness and protective efficacy to gather evidence of its potential impact on health outcomes. Five monthly cycles of SMC will be implemented between June and October 2022 in one county, Aweil South, in Northern Bahr el Gazal state.
The study will comprise the following six components :
- Two cross-sectional surveys at the height of the malaria season to explore impact on malaria incidence
- End-of-round survey
- Prospective protective efficacy cohort study to determine if SPAQ provides 28 days of protection from infection and whether drug concentrations and/or resistance influence the duration of protection
- Resistance markers study in children 3-59 months in the two research counties plus the two standard intervention counties to measure changes in resistance marker prevalence over time (pre and post within the same year and between years)
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- None
入排标准
- 年龄范围
- 3 Months 至 59 Months（Child）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Being resident in the project area
- •Afebrile with no other malaria associated symptoms in the past 48 hours or at time of recruitment
- •Consent to participate in the study obtained
- •Can comply with 3 day DOT of standard SPAQ regimen (day 0-2)
- •Willingness and ability of the childs guardians to comply with the study protocol for the duration of the study including all dry blood spot and slide collections
排除标准
- •Symptoms of malaria (tympanic fever ≥ 37.5 °C or history of fever in past 48 hours)
- •Known allergy to medicine provided
- •Receiving a sulfa-based medication for treatment or prophylaxis, including co-trimoxazole (trimethoprim-sulfamethoxazole).
- •Individuals receiving azithromycin due to the antimalarial activity of azithromycin.
- •Severe malnutrition according to WHO guidelines
- •Recruited in cross sectional surveys or any other SMC studies.
- •Children with HIV
- •Previous treatment with Amodiaquine in the past 28 days (treatment with ASAQ or SPAQ)
研究组 & 干预措施
Sulfadoxine-Pyrimethamine + Amodiaquine (SPAQ)
Children aged 3-59 months will receive SPAQ in the intervention arm
干预措施: Sulfadoxine pyrimethamine (Drug)
Sulfadoxine-Pyrimethamine + Amodiaquine (SPAQ)
Children aged 3-59 months will receive SPAQ in the intervention arm
干预措施: Amodiaquine (Drug)
结局指标
主要结局
Malaria incidence in study population in intervention county and eligible children in one control county
时间窗: Five months
Number of malaria cases in the intervention population and eligible children in one control county over the study period as reported through care givers in cross-sectional surveys at baseline, mid-intervention and endline
Prevalence of antimalarial resistance markers (dhfr, dhps, Pfcrt, pfmdr1) among chemoprevention failures as defined in outcome 2
时间窗: One month
All Dried blood spots (DBS) will be analysed for malaria mutation genotypes (dhfr, dhps, Pfcrt, pfmdr1) on baseline and endline and additionally on day 7, day 28, or if participant slide is positive for parasites on day 7 or an infection is reported through care givers in cross-sectional survey.
Drug concentrations of Sulfadoxine-pyrimethamine and amodiaquine among chemoprevention failures (as defined in outcome 1)
时间窗: One month
Drug concentrations will be analyzed for all samples on baseline, day 7 and day 28 and will be linked to chemoprevention failure cases as defined in outcome 2 or a malaria infection is reported through care givers in cross sectional survey.
Chemoprevention failure as defined by positive parasites in malaria slides after day 7 or positive qPCR in dried blood spot (DBS) on day 28
时间窗: One month
Malaria slides and dry blood spots (DBS) taken at days 0,7, 28 will be analysed with qPCR methodology to detect low level submicroscopic parasitemia in children treated with SPAQ
次要结局
未报告次要终点