Design of a cluster randomized trial assessing integrated infectious diseases training and on-site support for midlevel practitioners in Uganda

S. Naikoba, R. Colebunders, J. V. Geertruyden, K. Willis, S. Kinoti, Milly Namaalwa Kulubya, M. Mbonye, A. Miceli, L. Mpanga-Sebuyira, A. Ronald, M. Scheld, M. Weaver
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引用次数: 13

Abstract

SummaryTraining mid-level practitioners (MLP), usually nurses or clinical officers, to perform tasks conventionally assigned todoctors increases access to care and addresses health worker shortages in resource-constrained countries. In the face ofthe shortcomings of traditional training approaches, identification of effective training methods that create and maintainhighly competent MLP is a priority. A cluster randomized trial with pre–post components was conducted between Marchand December 2010 at 36 subdistrict health centres in Uganda. Eighteen out of the 36 health centres were randomized tothe intervention (Arm A) to receive sequenced integrated infectious diseases training for two MLPs followed by integratedinfectious diseases on-site support for the health worker teams once a month for nine months and 18 were randomized toreceive only sequenced training for two MLPs but no on-site support (Arm B). Outcomes measured included individualMLP knowledge and competence scores from written and observed clinical assessments; health facility performanceagainst indicators of care for malaria, tuberculosis and HIV as determined from patient care records; and mortalityamong children under five years during the project period measured using survey methods. Trial Registration: ClinicalTrials-NIH NCT01190540.
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设计一项集群随机试验,评估乌干达中级从业人员的综合传染病培训和现场支持
培训中级从业人员(MLP),通常是护士或临床官员,以执行传统上分配给医生的任务,增加获得护理的机会,并解决资源有限国家卫生工作者短缺的问题。面对传统培训方法的不足,确定有效的培训方法,创造和维持高能力的MLP是一个优先事项。2010年3月至12月期间,在乌干达36个街道保健中心进行了一项具有岗前组成部分的聚类随机试验。36个卫生中心中的18个被随机分配到干预组(A组),接受两名mlp的综合传染病培训,然后为卫生工作者团队提供综合传染病现场支持,每月一次,持续9个月;18个被随机分配到只接受两名mlp的综合传染病培训,但没有现场支持(B组)。测量的结果包括个人mlp知识和能力得分,来自书面和观察临床评估;根据病人护理记录确定的疟疾、结核病和艾滋病毒护理指标的卫生设施绩效;在项目期间,五岁以下儿童的死亡率用调查方法测量。试验注册:ClinicalTrials-NIH NCT01190540。
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