The Challenging Process of Developing an Antenatal Social Intervention for Parents From Culturally Diverse Backgrounds to Reduce Postnatal Distress: A Participatory Action Research Study

IF 3 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES Health Expectations Pub Date : 2025-01-06 DOI:10.1111/hex.70135
Sophie Isobel, Kahala Dixon, Alison Tutt, Bridget Clay, Sylvia Lim-Gibson
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Abstract

Background

A lack of social support contributes to women from culturally diverse backgrounds experiencing higher rates of perinatal distress and lower rates of service engagement.

Objective/Methods

This participatory action research study aimed to understand what a culturally appropriate social intervention may look like for pregnant women from culturally diverse backgrounds. Field notes and qualitative transcripts were descriptively synthesised.

Results

Challenges of engaging with culturally diverse communities in the context of perinatal health services were identified. Cultural factors and practices were seen to impact upon service engagement, with parents more likely to seek support outside of health settings. Community members expressed frustrations with the lack of deep cultural sensitivity in the structure and delivery of health services. Clear definitions in scope and aim of any intervention were indicated, before further community engagement.

Discussion

Challenges in engaging individuals and services from diverse communities highlighted the risks of ideas embedded in oversimplified understandings based on cultural stereotypes and assumptions of homogeneity of experiences at the intersection of cultural diversity, perinatal distress and health services.

Conclusions

Deep cultural sensitivity requires an understanding of how members of population groups perceive and understand health and wellbeing to directly inform the development of any intervention. Attempting to design a culturally sensitive intervention for socially isolated and culturally diverse parents within mainstream health services, led to a paradoxical tension between attempting to address needs in culturally insensitive ways or not attempting to address the needs at all.

Patient or Public Contribution

Members of the public and people who identified as having lived experience of social isolation, cultural diversity or mental distress were engaged in the community consultation phase of the study.

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为来自不同文化背景的父母开发产前社会干预以减少产后痛苦的挑战过程:一项参与性行动研究。
背景:缺乏社会支持导致来自不同文化背景的妇女经历较高的围产期痛苦率和较低的服务参与率。目的/方法:本参与性行动研究旨在了解文化上适当的社会干预对于来自不同文化背景的孕妇可能是什么样的。实地记录和定性转录本描述性地合成。结果:确定了在围产期保健服务背景下与文化多样化社区接触的挑战。文化因素和做法被认为对服务参与有影响,父母更有可能在卫生机构之外寻求支持。社区成员对保健服务的结构和提供缺乏深刻的文化敏感性表示失望。在进一步的社区参与之前,明确了任何干预的范围和目标。讨论:在吸引来自不同社区的个人和服务方面所面临的挑战突出了基于文化陈规定型观念和文化多样性、围产期痛苦和保健服务交汇处的经验同质性假设的过于简化的理解所包含的思想的风险。结论:深厚的文化敏感性需要了解人口群体成员如何感知和理解健康和福祉,从而直接为任何干预措施的发展提供信息。试图在主流保健服务中为社会孤立和文化多样化的父母设计一种文化上敏感的干预措施,导致试图以文化上不敏感的方式满足需求或根本不试图满足需求之间的矛盾紧张。患者或公众的贡献:公众成员和那些认为自己经历过社会孤立、文化多样性或精神痛苦的人参与了研究的社区咨询阶段。
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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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