Lived Experience Participation in Suicide Prevention Activities in Australia, a Scoping Review

IF 3 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Hayley Purdon, Tania Pearce, Bess Jackson, Sarah Wayland, Myfanwy Maple
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引用次数: 0

Abstract

Introduction

Lived experience inclusion is considered best practice in suicide prevention activities. Despite this, research remains limited exploring how individuals with lived experience actively engage in suicide research and prevention activities. The current scoping review aimed to map and summarise the existing literature describing the ‘how’ of lived experience participation in Australia.

Methods

A scoping review according to the methodology of Arksey and O'Malley (2005) was undertaken with descriptive (e.g., study aims and methodology) and descriptive analytic data (such as key definitions and participation descriptors) being extracted from included studies.

Results

A total of 42 studies met the inclusion criteria and were published between 2016 and 2023. There were many gaps in the data extracted, with participation descriptors and definitions often not reported in the literature. The included studies lacked clear and consistent definitions and practices when involving people with lived experience.

Conclusion

Current processes for reporting experiences of lived experience participation in suicide prevention lack standardisation within peer-reviewed publications. This review notes that there are gaps in the literature; however, the evidence base is growing for research that reports on suicide prevention research and activities that involve people with lived experience.

Patient or Public Contribution

This study was created and undertaken by a PhD candidate with lived experience of thoughts of suicide, suicide attempt and caring for a loved one through suicide. A further team member has lived experience of being a suicide attempt survivor, continued thoughts of suicide and carer of family with suicidal thoughts. The study was informed by a Community Advisory Committee, of which four members have lived experience of suicide, with the remaining two having lived experience in areas where inclusion is paramount such as disability and suicide research. Ethics approval was not required for the participation of the Community Advisory Committee as they were providing advice only on the research conduct.

Abstract Image

生活经验参与自杀预防活动在澳大利亚,范围审查
生活经验融合被认为是预防自杀活动的最佳实践。尽管如此,研究仍然局限于探索有生活经验的个人如何积极参与自杀研究和预防活动。当前的范围审查旨在绘制和总结描述澳大利亚生活体验参与“如何”的现有文献。方法根据Arksey和O'Malley(2005)的方法进行范围综述,从纳入的研究中提取描述性(如研究目的和方法)和描述性分析数据(如关键定义和参与描述符)。结果2016年至2023年间共发表了42项符合纳入标准的研究。在提取的数据中有许多空白,文献中往往没有报告参与描述符和定义。纳入的研究在涉及有生活经验的人时缺乏明确和一致的定义和实践。结论:在同行评议的出版物中,目前报告参与自杀预防的生活经验的过程缺乏标准化。本综述注意到文献中存在空白;然而,关于自杀预防的研究报告和涉及有生活经验的人的活动的证据基础正在增加。本研究是由一位博士候选人创建和承担的,他有过自杀的想法,自杀未遂和通过自杀来照顾所爱的人的经历。另一名团队成员有自杀未遂的经历,一直有自杀的想法,照顾有自杀想法的家庭。这项研究是由一个社区咨询委员会提供的,其中四名成员有自杀经历,其余两名成员在残疾和自杀研究等包容性至关重要的领域有过经历。社区咨询委员会的参与不需要伦理批准,因为他们只提供关于研究行为的建议。
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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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