居住在联合王国的移民及其对参与健康研究的看法:一项混合方法研究

IF 3 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Mayuri Gogoi, Rebecca F. Baggaley, Luisa Silva, Zainab Lal, Holly Reilly, Vishant Modhwadia, Daniel Pan, Paul Bird, Laura Nellums, Manish Pareek
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引用次数: 0

摘要

移民参与卫生研究对于表达他们的需求和为循证实践提供信息至关重要。我们对居住在英国莱斯特的移民进行了一项混合方法研究,以了解他们对参与健康研究的看法以及影响参与的因素。方法采用问卷调查和重点小组调查的方法。还与主要线人进行了访谈和焦点小组讨论。这项研究在莱斯特的两个地点进行。问卷数据在r中进行描述性分析。COM-B框架用于对访谈和焦点小组记录进行主题分析。与移民出身的公众成员举办的讲习班有助于数据解释和分析。结果共完成119份问卷和4个焦点小组(n = 28)。对关键举报人进行了7次访谈和1次焦点小组(n = 7)。问卷调查的受访者来自34个不同的国家,其中很大一部分(25%)认为自己是寻求庇护者/难民。焦点小组中的移徙者来自16个不同国家,主要是寻求庇护者/难民(n = 18)。COM-B模型的三个组成部分(能力、机会和动机)被确定为主题,并使用问卷数据的描述性统计来补充16个子主题。个人能力,包括对研究的认识和感知、语言能力和使用技术的技能,对参与有重大影响。同时,研究发现,诸如成本、相互竞争的需求和优先事项、在联合王国获得医疗保健的机会和经验、语言障碍、学习和参与的机会、不稳定的生活条件以及社会文化规范和对健康的看法等机会的存在与否对参与研究很重要。参与研究的动机包括信任、研究背景、基于需求的研究、利他主义、渴望被倾听和接受激励。结论本研究为移民参与健康研究提供了有限的证据基础。我们的研究结果以COM-B模型为基础,展示了移民的动机如何受到一系列个人能力、环境和社会机会的影响,从而影响动机和影响研究参与行为。这些发现可能支持设计涉及服务不足群体的无障碍、包容、公平和有影响力的卫生研究。该项目的患者和公众参与和参与(PPIE)是通过EMBRACE(东米德兰兹移民研究咨询协作)小组获得的,该小组于2019年成立,是一个针对移民的咨询小组。我们招募了新的移民成员加入小组,并让他们参与研究结果的解释。我们与该小组组织了两次研讨会,在2024年2月举行的第一次研讨会上,九名成员参加了初步结果的审查,并就背景和解释数据提供了见解。研究小组考虑了在研讨会上收到的反馈,并将其整合到分析中。最终的分析在2024年9月再次提交给小组,在研讨会上进行的讨论对这份手稿的形成起到了重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Migrants Living in the United Kingdom and Their Perceptions of Participation in Health Research: A Mixed-Methods Study

Migrants Living in the United Kingdom and Their Perceptions of Participation in Health Research: A Mixed-Methods Study

Background

Migrants' participation in health research is essential to give voice to their needs and inform evidence-based practice. We conducted a mixed-methods study with migrants living in Leicester, United Kingdom, to understand their perceptions of participation in health research and factors influencing participation.

Methods

Our study included a questionnaire and focus groups with migrants. Interviews and focus groups were also conducted with key informants. The study was carried out at two sites in Leicester. Questionnaire data were analysed descriptively in R. The COM-B framework was used to thematically analyse interview and focus group transcripts. Workshops with public members of migrant origin helped with data interpretation and analysis.

Results

119 questionnaires and 4 focus groups (n = 28) were completed with migrants. Seven interviews and one focus group (n = 7) were conducted with key informants. Questionnaire respondents originated from 34 different countries, with a significant proportion (25%) identifying themselves as asylum seekers/refugees. Migrants in the focus groups were from 16 different countries and were mainly asylum seekers/refugees (n = 18). The three components of the COM-B model (Capability, Opportunity and Motivation) were identified as the main themes, and descriptive statistics from the questionnaire data have been used to supplement the 16 sub-themes. Individual capabilities encompassing awareness and perception of research, language abilities and skills in the use of technology significantly influenced participation. Simultaneously, the presence or absence of opportunities such as costs, competing needs and priorities, healthcare access and experiences in the United Kingdom, language barriers, opportunities for learning and taking part, precarious living conditions and socio-cultural norms and perceptions about health were found to be important for research participation. Motivations to take part in research included trust, context of the research, need-based research, altruism, desire to be heard and receiving incentives.

Conclusion

Our study contributes to the limited evidence base exploring migrants' participation in health research. Our findings, grounded in the COM-B model, exhibit how migrants' motivations, influenced by a host of individual capabilities and environmental and social opportunities, can influence motivation and impact research participation behaviour. These findings may support the design of accessible, inclusive, equitable and impactful health research involving underserved groups.

Patient or Public Contribution

Patient and Public Involvement and Engagement (PPIE) in the project was obtained through the EMBRACE (East Midlands Migrant Research Advisory Collaborative) group, which was created as a migrant specific advisory group in 2019. We recruited new migrant members into the group and involved them in the interpretation of the study results. We organised two workshops with the group, and in the first workshop, held in February 2024, nine members took part to review the preliminary results and offer insights in contextualising and interpreting the data. The research team took into consideration the feedback received at the workshop and integrated it into the analysis. The final analysis was presented to the group again in September 2024, and the discussions held at that workshop were instrumental in shaping this 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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