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乌干达宫颈癌预防“变革者”混合实施-效果试验的研究方案

Study protocol for a hybrid implementation-effectiveness trial of Game Changers for Cervical Cancer Prevention in Uganda.

作者信息

Wagner Glenn J, Bogart Laura M, Matovu Joseph K B, Gwokyalya Violet, Beyeza-Kashesya Jolly, Ober Allison, Green Harold D, Nakami Sylvia, Juncker Margrethe, Namisango Eve, Luyirika Emmanuel, McBain Ryan K, Bouskill Kathryn, Wanyenze Rhoda K

机构信息

RAND Corporation, Santa Monica, California, United States of America.

Department of Medicine, Charles R. Drew University of Medicine and Science, Los Angeles, California, United States of America.

出版信息

PLoS One. 2025 Jan 24;20(1):e0317491. doi: 10.1371/journal.pone.0317491. eCollection 2025.

Abstract

INTRODUCTION

Cervical cancer (CC) is the leading cause of cancer-related deaths among Uganda women, yet rates of CC screening are very low. Training women who have recently screened to engage in advocacy for screening among women in their social network is a network-based strategy for promoting information dissemination and CC screening uptake.

METHODS

Drawing on the Exploration, Preparation, Implementation and Sustainment (EPIS) framework for implementation science, this hybrid type 1 randomized controlled trial (RCT) of a peer-led, group advocacy training intervention, Game Changers for Cervical Cancer Prevention (GC-CCP), will examine efficacy for increasing CC screening uptake as well as how it can be implemented and sustained in diverse clinic settings. In the Preparation phase we will prepare the four study clinics for implementation of GC-CCP and the expected increase in demand for CC screening, by using qualitative methods (stakeholder interviews and client focus groups) to identify and address structural barriers to easy access to CC screening. In the Implementation phase, GC-CCP will be implemented over 36 months at each clinic, with screened women (index participants) enrolled as research participants receiving the intervention in the first 6 months as part of a parallel group RCT overseen by the research study team to evaluate efficacy for CC screening uptake among their enrolled social network members. All research participants will be assessed at baseline and months 6 and 12. Intervention implementation and supervision will then be transitioned to clinic staff and offered as part of usual care in the subsequent 30 months as part of the Sustainability phase. Using the RE-AIM framework, we will evaluate engagement in GC-CCP and CC advocacy (reach), alter CC screening (effectiveness), adoption into clinic operations, implementation outcomes (acceptability, feasibility, fidelity, cost-effectiveness) and maintenance.

DISCUSSION

This is one of the first studies to use a network-driven approach and empowerment of CC screened peers as change agents to increase CC screening. If shown to be an effective and sustainable implementation strategy for promoting CC screening, this peer advocacy model could be applied to other preventative health behaviors and disease contexts.

TRIAL REGISTRATION

NIH Clinical Trial Registry NCT06010160 (clinicaltrials.gov; date: 8/17/2023).

摘要

引言

宫颈癌(CC)是乌干达女性癌症相关死亡的主要原因,但宫颈癌筛查率非常低。培训近期接受过筛查的女性,让她们在其社交网络中为女性进行筛查宣传,这是一种基于网络的策略,用于促进信息传播和提高宫颈癌筛查的接受度。

方法

借鉴实施科学的探索、准备、实施和维持(EPIS)框架,这项1型混合随机对照试验(RCT)针对由同伴主导的团体宣传培训干预措施“宫颈癌预防的变革者”(GC-CCP),将检验其在提高宫颈癌筛查接受度方面的效果,以及如何在不同的诊所环境中实施和维持该干预措施。在准备阶段,我们将通过定性方法(利益相关者访谈和客户焦点小组),为四家研究诊所准备实施GC-CCP以及应对宫颈癌筛查需求预期增加的情况,以识别并解决影响便捷获取宫颈癌筛查的结构障碍。在实施阶段,GC-CCP将在每家诊所持续实施36个月,已接受筛查的女性(索引参与者)作为研究参与者,在前6个月接受干预,这是由研究团队监督的平行组RCT的一部分,以评估其在已登记的社交网络成员中提高宫颈癌筛查接受度的效果。所有研究参与者将在基线、第6个月和第12个月接受评估。然后,干预措施的实施和监督将移交给诊所工作人员,并在随后的30个月作为维持阶段的一部分,作为常规护理的一部分提供。使用RE-AIM框架,我们将评估对GC-CCP和宫颈癌宣传的参与度(覆盖范围)、改变宫颈癌筛查情况(有效性)、纳入诊所运营情况、实施结果(可接受性、可行性、保真度、成本效益)以及维持情况。

讨论

这是首批使用网络驱动方法并赋予接受宫颈癌筛查的同伴作为变革推动者的权力来增加宫颈癌筛查的研究之一。如果被证明是促进宫颈癌筛查的有效且可持续的实施策略,这种同伴宣传模式可应用于其他预防性健康行为和疾病背景。

试验注册

美国国立卫生研究院临床试验注册中心NCT06010160(clinicaltrials.gov;日期:2023年8月17日)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/182e/11760014/590ec13c5960/pone.0317491.g001.jpg

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