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比较两种预先医疗照护计划谈话活动,以激励美国服务欠缺社区完成预先医疗指示:美国项目谈话试验,针对群组、随机对照试验的研究方案。

Comparing two advance care planning conversation activities to motivate advance directive completion in underserved communities across the USA: The Project Talk Trial study protocol for a cluster, randomized controlled trial.

机构信息

Department of Medicine, Penn State College of Medicine, 500 University Dr., H-041, Hershey, PA, 17033-0850, USA.

Department of Humanities, Penn State College of Medicine, 500 University Drive, Hershey, PA, 17036, USA.

出版信息

Trials. 2022 Sep 30;23(1):829. doi: 10.1186/s13063-022-06746-3.

DOI:10.1186/s13063-022-06746-3
PMID:36180899
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9523194/
Abstract

BACKGROUND

Advance care planning (ACP) is a process involving conversations between patients, loved ones, and healthcare providers that consider patient preferences for the types of medical therapies received at the end of life. Underserved populations, including Black, Hispanic, rural, and low-income communities are less likely to engage in ACP than other communities, a health inequity that results in lower-quality care and reduced hospice utilization. The purpose of this trial is to compare efficacy of two interventions intended to motivate ACP (particularly advance directive completion) for those living in underserved communities.

METHODS

This 3-armed cluster, randomized controlled mixed methods design is being conducted in 75 community venues in underserved communities across the USA. The goal of the trial is to compare the efficacy of two interventions at motivating ACP. Arm 1 uses an end-of-life conversation game (Hello); Arm 2 uses a nationally utilized workshop format for ACP conversations (The Conversation Project); and Arm 3 uses an attention control game (TableTopics). Events are held in partnership with 75 local community-based host organizations and will involve 1500 participants (n=20 per event). The primary outcome is completion of a visually verified advance directive at 6 months post-event. Primary analyses compare efficacy of each intervention to each other and the control arm. Secondary mixed methods outcomes include (a) other ACP behaviors and engagement; (b) communication quality; (c) impact of sociocultural environment on ACP (via qualitative interviews); and (d) implementation and sustainability. Subgroup analyses examine outcomes for Black, Hispanic, and rural groups in particular.

DISCUSSION

This trial will add to the evidence base behind various conversational ACP interventions, examine potential mechanisms of action for such interventions, and provide qualitative data to better understand the sociocultural environment of how community-based ACP interventions are experienced by underserved populations. Results will also provide important data for future researchers to learn whether visual verification of advance directives is necessary or whether reliance on self-reported outcomes is of comparable value. Data from this study will inform ways to effectively motivate underserved communities to participate in advance care planning.

TRIAL REGISTRATION

ClinicalTrials.gov NCT04612738. Registered on October 12, 2020. All information from the WHO Trial Registration Data Set can be found within the protocol.

摘要

背景

预先医疗指示(advance care planning,ACP)是一个涉及患者、家属和医疗保健提供者之间对话的过程,旨在考虑患者对生命末期接受的医疗治疗类型的偏好。与其他社区相比,服务不足的人群(包括黑种人、西班牙裔、农村和低收入社区)参与 ACP 的可能性较低,这是一种健康不平等现象,导致护理质量下降和减少使用临终关怀。本试验的目的是比较两种旨在激励服务不足社区进行 ACP(特别是预先医疗指示的完成)的干预措施的效果。

方法

这是一项 3 臂聚类、随机对照混合方法设计,在美国各地的服务不足社区的 75 个社区场所进行。该试验的目的是比较两种干预措施在激励 ACP 方面的效果。第 1 组使用生命末期对话游戏(Hello);第 2 组使用全国范围内用于 ACP 对话的讲习班形式(对话项目);第 3 组使用注意力控制游戏(TableTopics)。活动与 75 个当地的社区主办组织合作进行,将涉及 1500 名参与者(每个活动 20 名)。主要结局是在活动结束后 6 个月完成经视觉验证的预先医疗指示。主要分析比较每种干预措施与其他干预措施和对照组的效果。次要混合方法结果包括:(a)其他 ACP 行为和参与度;(b)沟通质量;(c)社会文化环境对 ACP 的影响(通过定性访谈);(d)实施和可持续性。亚组分析特别针对黑种人、西班牙裔和农村群体的结果进行分析。

讨论

本试验将为各种对话式 ACP 干预措施的证据基础提供补充,研究这些干预措施的潜在作用机制,并提供定性数据,以更好地了解社区为基础的 ACP 干预措施在服务不足人群中是如何被体验的社会文化环境。结果还将为未来的研究人员提供重要数据,以了解视觉验证预先医疗指示是否必要,或者依赖自我报告的结果是否具有同等价值。本研究的数据将为如何有效地激励服务不足的社区参与预先医疗计划提供信息。

试验注册

ClinicalTrials.gov NCT04612738。于 2020 年 10 月 12 日注册。世界卫生组织试验注册数据集中的所有信息都可以在方案中找到。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4be/9524016/ced09a681d02/13063_2022_6746_Fig3_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4be/9524016/122fa20e63cf/13063_2022_6746_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4be/9524016/6dd7c20edca8/13063_2022_6746_Fig2_HTML.jpg
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