Evaluating parent and public involvement activities within a paediatric palliative care research centre: Route map to impactful and meaningful engagement.

IF 3.6 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES
Palliative Medicine Pub Date : 2024-10-01 Epub Date: 2024-08-10 DOI:10.1177/02692163241266374
Laura Barrett, Julia Hackett, Jo Taylor, Andrew Papworth, Gabriella Walker, Lorna Fraser
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引用次数: 0

Abstract

Background: Patient and Public Involvement (PPI) is an important component of healthcare research. Conducting PPI within paediatric palliative care research requires specific ethical and practical considerations. Regular reviews of PPI activity are important.

Aim: To evaluate a paediatric palliative care research centre's PPI activity to determine what went well, or less well; and how future activities can be improved.

Design: Two stage evaluation: first a review of PPI study logs; second a qualitative exploration using a survey, structured interviews and a focus group. Data were analysed thematically.

Settings/participants: Parents of children with life-limiting conditions, bereaved parents and researchers, all engaged in PPI activity within a paediatric palliative care research centre.

Findings: The review of PPI logs for 15 studies highlighted the crucial role of funding in enabling PPI throughout the research. Eight parents completed the survey, 4 parents were interviewed and 12 researchers participated in a focus group. Three themes were developed: Clarity of processes and purpose; balanced relationships created a safe space; and mutual respect and value for PPI. These themes highlight what is working well within the Centre's approach to PPI and the opportunities to improve.

Conclusions: To undertake meaningful PPI in paediatric palliative care research, adequate time and resources are required. Roles, processes and expectations must be explicitly agreed. Establishing relationships ensures trust and enables authenticity and vulnerability. In addition to improving research, PPI has personal benefits for researchers and parents. The evaluation led to the development of a 'route map' for establishing an impactful PPI group for paediatric palliative care research.

评估儿科姑息关怀研究中心的家长和公众参与活动:有影响、有意义的参与路线图。
背景:患者和公众参与(PPI)是医疗保健研究的重要组成部分。在儿科姑息关怀研究中开展患者和公众参与需要考虑特定的伦理和实际问题。目的:评估儿科姑息关怀研究中心的患者和公众参与活动,以确定哪些活动开展得好,哪些活动开展得不好,以及如何改进未来的活动:设计:分两个阶段进行评估:首先审查公众宣传研究日志;其次通过调查、结构化访谈和焦点小组进行定性探索。对数据进行专题分析:环境/参与者:患有危重症儿童的家长、失去亲人的家长和研究人员,他们都在儿科姑息关怀研究中心参与了公众宣传活动:对 15 项研究的公众参与日志进行审查后发现,在整个研究过程中,资金在促进公众参与方面发挥着至关重要的作用。8 位家长完成了调查,4 位家长接受了访谈,12 位研究人员参加了焦点小组。形成了三个主题:明确程序和目的;平衡关系创造安全空间;相互尊重和重视公众宣传。这些主题突出了该中心在公众宣传方面行之有效的方法以及需要改进的地方:要在儿科姑息关怀研究中开展有意义的公众参与,需要充足的时间和资源。必须明确商定角色、流程和期望。建立关系可确保信任,并使真实性和脆弱性成为可能。除了改进研究之外,公众参与还能为研究人员和家长带来个人利益。通过评估,为建立一个有影响力的儿科姑息关怀研究公众参与小组制定了 "路线图"。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Palliative Medicine
Palliative Medicine 医学-公共卫生、环境卫生与职业卫生
CiteScore
7.60
自引率
9.10%
发文量
125
审稿时长
6-12 weeks
期刊介绍: Palliative Medicine is a highly ranked, peer reviewed scholarly journal dedicated to improving knowledge and clinical practice in the palliative care of patients with far advanced disease. This outstanding journal features editorials, original papers, review articles, case reports, correspondence and book reviews. Essential reading for all members of the palliative care team. This journal is a member of the Committee on Publication Ethics (COPE).
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