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及时的短期专业姑息治疗服务干预对脆弱的老年人及其初级保健中的家庭照顾者:一项试点随机对照试验的研究方案。

Timely short-term specialised palliative care service intervention for frail older people and their family carers in primary care: study protocol for a pilot randomised controlled trial.

机构信息

End-of-Life Care Research Group, Department of Family Medicine and Chronic Care, Vrije Universiteit Brussel, Brussels, Belgium

End-of-Life Care Research Group, Department of Family Medicine and Chronic Care, Vrije Universiteit Brussel, Brussels, Belgium.

出版信息

BMJ Open. 2021 Jan 20;11(1):e043663. doi: 10.1136/bmjopen-2020-043663.

Abstract

INTRODUCTION

There is limited evidence regarding the effectiveness of timely integration of short-term specialised palliative care services for older people in primary care. Using a Theory of Change approach, we developed such an intervention, the Frailty+ intervention. We present the protocol of a pilot randomised controlled trial (RCT) with a process evaluation that aims to assess the feasibility and preliminary effectiveness of the Frailty+ intervention.

METHODS AND ANALYSIS

We will conduct a pilot RCT in Flanders, Belgium. Frail older people who are discharged to home from hospital will be identified and recruited. Seventy-six will be randomly assigned either to the control group (standard care) or the intervention group (Frailty+ intervention alongside standard care). Data will be collected from patients and family carers. At the core of the Frailty+ intervention is the provision of timely short-term specialised palliative care facilitated by a nurse from the specialised palliative home care service over a period of 8 weeks. We will assess feasibility in terms of recruitment, randomisation, acceptability of the intervention, retention in the programme and data completion. The primary outcome for assessing preliminary effectiveness is a mean score across five key symptoms that are amenable to change (ie, breathlessness, pain, anxiety, constipation, fatigue), measured at baseline and 8 weeks post-baseline. The process evaluation will be conducted in the intervention group only, with measurements at 8-11 weeks post-baseline to evaluate implementation, mechanisms of change and contextual factors.

ETHICS AND DISSEMINATION

The study has been approved by the ethics committee of University Hospital Ghent. Results will be used to inform the design of a full-scale RCT and will be published in a peer-reviewed, open access journal.

TRIAL REGISTRATION NUMBER

ISRCTN39282347; Pre-results.

摘要

简介

关于在初级保健中及时整合短期专业姑息治疗服务对老年人的有效性,证据有限。我们使用变革理论方法,开发了这样一种干预措施,即脆弱+干预措施。我们提出了一项试点随机对照试验 (RCT) 的方案,该方案结合了一项过程评估,旨在评估脆弱+干预措施的可行性和初步效果。

方法和分析

我们将在比利时佛兰德斯进行一项试点 RCT。从医院出院回家的体弱老年人将被识别并招募。76 名将被随机分配到对照组(标准护理)或干预组(脆弱+干预与标准护理一起)。数据将从患者和家庭护理人员收集。脆弱+干预的核心是在 8 周的时间内,由专门的姑息家庭护理服务的护士提供及时的短期专业姑息治疗。我们将根据招募、随机化、干预的可接受性、对计划的保留和数据完成情况评估可行性。评估初步效果的主要结果是五个可改变的关键症状的平均评分(即呼吸困难、疼痛、焦虑、便秘、疲劳),在基线和基线后 8 周测量。过程评估仅在干预组进行,在基线后 8-11 周进行测量,以评估实施、变化机制和背景因素。

伦理和传播

该研究已获得根特大学医院伦理委员会的批准。结果将用于为全面的 RCT 设计提供信息,并将在同行评议的开放获取期刊上发表。

试验注册号

ISRCTN39282347;预结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/add7/8483035/b7cc4ebe61cc/bmjopen-2020-043663f01.jpg

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