Co-Producing and Evaluating a Culturally Inclusive Dementia Education Initiative: A Multimethod Study Protocol

IF 3 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Gabriela Caballero, Ann Dadich, Michelle DiGiacomo, Nicky Morrison, Charles Okafor, Joyce Siette, Genevieve Z. Steiner-Lim, Dementia Friends Unite Stakeholders, Diana Karamacoska
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引用次数: 0

Abstract

Introduction

Limited dementia awareness among culturally and linguistically diverse communities can exacerbate stigma and hinder support for carers and people at risk of or living with dementia. Co-producing a culturally inclusive dementia education intervention with representative stakeholders can address these knowledge and service gaps. This paper details the protocol for designing and evaluating a co-produced multilingual dementia education intervention named Dementia Friends Unite. This project aims to improve dementia knowledge, attitudes and supportive practices in a multicultural context.

Method

This project will be conducted in South Western Sydney, Australia, where Arabic, Cantonese, English, Greek, Mandarin and Vietnamese are the most common languages spoken. A multi-stakeholder collaboration involving representatives from each of these communities was formed to co-produce the multilingual dementia education intervention. Two studies are planned to explore the co-production process and evaluate the intervention's impact, guided by implementation science frameworks. Study 1 will examine stakeholder and researcher experiences in co-production through minuted meetings and responses to the patient and public engagement evaluation tool. Data will be descriptively analysed to identify the barriers and facilitators to co-production. Study 2 involves evaluating the initiative's impact according to the RE-AIM framework. Outcome measures include intervention reach and effectiveness in changing participants' knowledge, attitudes and supportive practices through questionnaires (pre-, post- and follow-up) and interviews; adoption and implementation characteristics through focus groups with stakeholders and facilitators; and maintenance through a cost–benefit analysis.

Conclusion

This project will employ a comprehensive approach to address unmet needs and research gaps in co-produced dementia education and its implementation in multicultural contexts. It can serve as a blueprint for others seeking to engage culturally diverse populations in community-based health education and research.

Patient or Public Contribution

A multi-stakeholder collaboration involving representatives from local government and care services, as well as people with living and caring experiences of dementia, from each of the targeted communities, was formed to co-produce this initiative. Their involvement spans study design, conduct, interpretation of findings and dissemination.

共同制定和评估文化包容性痴呆教育倡议:一项多方法研究方案
在文化和语言多样化的社区中,对痴呆症的认识有限可能会加剧耻辱感,并阻碍对护理人员和面临痴呆症风险或患有痴呆症的人的支持。与具有代表性的利益攸关方共同制定具有文化包容性的痴呆症教育干预措施,可以解决这些知识和服务差距。本文详细介绍了设计和评估共同制作的多语言痴呆症教育干预措施的方案,称为痴呆症之友联合。该项目旨在在多元文化背景下改善痴呆症知识、态度和支持实践。本项目将在澳大利亚悉尼西南部进行,阿拉伯语、粤语、英语、希腊语、普通话和越南语是最常用的语言。来自这些社区的代表组成了多方利益相关者合作,共同制定多语言痴呆症教育干预措施。在实施科学框架的指导下,计划进行两项研究,以探索合作生产过程并评估干预措施的影响。研究1将通过会议记录和对患者和公众参与评估工具的回应来检查利益相关者和研究人员在合作生产中的经验。将对数据进行描述性分析,以确定合作制作的障碍和促进因素。研究2包括根据RE-AIM框架评估计划的影响。结果测量包括通过问卷调查(事前、事后和随访)和访谈改变参与者的知识、态度和支持性做法的干预范围和有效性;通过与利益相关者和促进者进行焦点小组讨论的采用和实施特点;通过成本效益分析进行维护。本项目将采用综合方法解决联合制作的痴呆症教育及其在多元文化背景下的实施中未满足的需求和研究差距。它可以作为其他寻求使文化多样化的人口参与社区卫生教育和研究的国家的蓝图。来自地方政府和护理服务机构的代表以及来自每个目标社区的有痴呆症生活和护理经验的人组成了多方利益攸关方合作,共同开展这一行动。他们的参与范围包括研究设计、实施、研究结果的解释和传播。
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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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