与公众共同开发的戏剧作为传播敏感主题研究的一种形式的可接受性、安全性和影响。

IF 3 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Cat Papastavrou Brooks, Noreen Hopewell-Kelly, Natalia V. Lewis
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引用次数: 0

摘要

简介患者和公众参与(PPI)以及研究成果的传播是产生研究影响的关键环节;然而,传统方法往往无法吸引非学术界受众的参与。创造性的方法(如共同开发的戏剧)可以有效地使研究过程和研究结果更吸引人、更容易为公众所接受。对于如何让患者和公众安全地参与到传播敏感话题研究成果的戏剧的开发和演出中,我们所知甚少。在一项针对有家庭虐待史的女性的正念研究中,一个公众参与小组的成员共同开发并表演了一出关于她们经历的戏剧。本研究旨在评估共同开发的剧本在宣传 PPI 和家庭虐待研究成果时的影响、可接受性和安全性:我们与剧组和观众一起进行了一项混合方法研究。我们从观众中收集了 20 份定量调查问卷和 56 份定性调查问卷,对话剧表演进行了 4.25 小时的直接观察,并采访了 7 名观众和 8 名话剧团队成员。我们使用框架法和描述性统计对数据进行了分析,采用 "顺藤摸瓜 "的方法将定性和定量结果整合到主题中,以实现我们的研究目标:我们提出了三个综合主题和十个次主题。价值 "主题概括了戏剧对观众理解的影响、潜在的影响机制及其在传播深度和广度上的有效性。再次创伤 "主题描述了戏剧的潜在危害、演员再次创伤的风险以及观众的痛苦。降低风险 "主题总结了降低这些伤害风险的方法:由参与研究的 PPI 成员共同开发并演出的话剧提高了人们对家庭虐待的认识。然而,对于该剧在传播关于敏感主题研究中的公众宣传信息方面的价值,存在不同意见。话剧在研究传播中的价值与其调动公众情感的能力和可获得性有关。建议实施相关策略,降低观众和项目团队再次受到创伤的风险:患者或公众的贡献:每个有共同创作和表演该剧直接经验的人都为本研究做出了贡献。其中包括四位公众贡献者:一位社区剧院制片人、两位有家庭虐待经历的演员(他们都是研究 PPI 小组的成员)以及一位已经在社区剧院工作的社区演员。我们与公众参与小组成员举办了一次参与式研讨会,利用公众参与评估工具 "立方体 "来完善我们的研究问题和数据收集工具。公众参与小组成员对手稿草稿进行了检查并提出了意见。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Acceptability, Safety and Impact of a Play Co-Developed With Public Contributors as a Format for Disseminating Research on a Sensitive Subject

Introduction

Patient and public involvement (PPI) and dissemination of research findings are key parts of the pathway to research impact; however, traditional approaches often fail to engage non-academic audiences. Creative methods such as co-developed plays can be effective ways of making the research process and findings more engaging and accessible to the public. Not much is known about how to safely involve patients and the public in the development and delivery of plays disseminating research on sensitive subjects. Members of a PPI group on a study about mindfulness for women with a history of domestic abuse co-developed and performed a play about their experiences. This study aimed to evaluate the impact, acceptability and safety of a co-developed play in publicizing PPI and findings from research on domestic abuse.

Methods

We conducted a mixed-methods study with the play team and audience. We collected 20 quantitative and 56 qualitative survey responses from audience members, carried out 4.25 h of direct observations of play performances and interviewed seven audience members and eight play team members. Data were analyzed using the framework method and descriptive statistics, using a ‘following a thread’ approach to integrate qualitative and quantitative findings in themes answering our study aim.

Findings

We developed three integrated themes with ten sub-themes. The ‘Value’ theme summarized the plays' impact on audience understanding, potential mechanisms of impact and its effectiveness in depth over breadth of dissemination. The ‘Re-traumatization’ theme described potential harms of the play, the risks of re-traumatizing actors and distressing audiences. The ‘Reducing the risks’ theme summarized ways of reducing these risks of harm.

Conclusion

A play co-developed and performed by study PPI members raised awareness of domestic abuse. However, there were divergent opinions on its value in disseminating messages about PPI in research on sensitive subjects. The value of the play for research dissemination was linked to its ability to emotionally engage the public, and to its accessibility. Implementing strategies to reduce the risk of re-traumatizing audience members and the project team is recommended.

Patient or Public Contribution

Everyone with direct experience of co-creating and performing the play contributed to this study. This included four public contributors: a community theatre producer, two actors with lived experience of domestic abuse who were members of the study PPI group and one community actor already working with the community theatre. A participatory workshop with PPI contributors was held to refine our research questions and data collection instruments, using a public involvement evaluation tool, The Cube. PPI contributors checked and commented on the draft manuscript.

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来源期刊
Health Expectations
Health Expectations 医学-公共卫生、环境卫生与职业卫生
CiteScore
5.20
自引率
9.40%
发文量
251
审稿时长
>12 weeks
期刊介绍: Health Expectations promotes critical thinking and informed debate about all aspects of patient and public involvement and engagement (PPIE) in health and social care, health policy and health services research including: • Person-centred care and quality improvement • Patients'' participation in decisions about disease prevention and management • Public perceptions of health services • Citizen involvement in health care policy making and priority-setting • Methods for monitoring and evaluating participation • Empowerment and consumerism • Patients'' role in safety and quality • Patient and public role in health services research • Co-production (researchers working with patients and the public) of research, health care and policy Health Expectations is a quarterly, peer-reviewed journal publishing original research, review articles and critical commentaries. It includes papers which clarify concepts, develop theories, and critically analyse and evaluate specific policies and practices. The Journal provides an inter-disciplinary and international forum in which researchers (including PPIE researchers) from a range of backgrounds and expertise can present their work to other researchers, policy-makers, health care professionals, managers, patients and consumer advocates.
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