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The PRIME trial protocol: evaluating the impact of an intervention implemented in public health centres on management of malaria and health outcomes of children using a cluster-randomised design in Tororo, Uganda

机译:PRIME试验方案:在乌干达托罗罗采用集群随机设计,评估在公共卫生中心实施的干预措施对儿童疟疾管理和儿童健康结局的影响

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Background In Africa, inadequate health services contribute to the lack of progress on malaria control. Evidence of the impact of interventions to improve health services on population-level malaria indicators is needed. We are conducting a cluster-randomised trial to assess whether a complex intervention delivered at public health centres in Uganda improves health outcomes of children and treatment of malaria, as compared to the current standard of care. Methods/Design Twenty public health centres (level II and III) in Tororo district will be included; 10 will be randomly assigned to the intervention and 10 to control. Clusters will include households located within 2 km of health centres. The trial statistician will generate the random allocation sequence and assign clusters. Health centres will be stratified by level, and restricted randomisation will be employed to ensure balance on cluster location and size. Allocation will not be blinded. The intervention includes training in health centre management, fever case management with use of rapid diagnostic tests (RDTs) for malaria, and patient-centered services, and provision of artemether-lumefantrine (AL) and RDTs when stocks run low. The impact of the intervention on population-level health indicators will be assessed through community surveys conducted at baseline in randomly selected children from each cluster, and repeated annually for two years. The impact on individuals over time will be assessed in a cohort study of children recruited from households randomly selected per cluster. The impact on health centres will be assessed using patient exit interviews, monthly surveillance, and assessment of health worker knowledge and skills. The primary outcome is the prevalence of anaemia (haemoglobin <11.0 g/dL) in individual children under five measured in the annual community surveys. The primary analysis will be based on the cluster-level results. Discussion The PRIME trial findings will be supplemented by the PROCESS study, an evaluation of the process, context, and wider impact of the PRIME intervention which will be conducted alongside the main trial, together providing evidence of the health impact of a public sector intervention in Uganda. Trial registration and funding This trial is registered at Clinicaltrials.gov (NCT01024426) and is supported by the ACT Consortium.
机译:背景技术在非洲,医疗服务不足导致疟疾控制缺乏进展。需要有证据证明改善卫生服务的干预措施对人口水平疟疾指标的影响。我们正在进行一项整群随机试验,以评估与目前的标准护理相比,乌干达公共卫生中心提供的复杂干预措施是否能够改善儿童的健康状况和治疗疟疾。方法/设计将包括Tororo区的20个公共卫生中心(II级和III级); 10个将随机分配给干预,10个进行控制。集群将包括位于保健中心2公里以内的家庭。试验统计员将生成随机分配序列并分配聚类。卫生中心将按级别进行分层,并且将采用有限的随机化以确保群集位置和大小上的平衡。分配不会盲目。干预措施包括培训卫生中心管理,使用疟疾快速诊断检测(RDT)进行发烧病例管理以及以患者为中心的服务,以及在存量不足时提供蒿甲醚-萤石素(AL)和RDT。干预措施对人群健康指标的影响将通过在基线时对来自每个群体的随机选择的儿童进行社区调查来评估,并每年重复两年。随时间推移对个人的影响将在一项针对从每个聚类中随机选择的家庭招募的孩子的队列研究中进行评估。将通过患者出诊访谈,每月监督以及评估卫生工作者的知识和技能来评估对卫生中心的影响。主要结果是在年度社区调查中测得的五岁以下儿童的贫血患病率(血红蛋白<11.0 g / dL)。主要分析将基于群集级别的结果。讨论PRIME试验结果将由PROCESS研究,对PRIME干预的过程,背景和更广泛影响的评估进行补充,并将与主要试验一起进行,一起提供公共部门干预对健康的健康影响的证据。乌干达。试验注册和资助该试验已在Clinicaltrials.gov(NCT01024426)上注册,并得到ACT联合会的支持。

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