School of Medical, Indigenous and Health Sciences, University of Wollongong, Wollongong, New South Wales, Australia.
Health Expect. 2024 Dec;27(6):e70091. doi: 10.1111/hex.70091.
People newly diagnosed with multiple sclerosis (MS) often pursue 'health-related' behaviour changes to feel in control of their diagnosis. However, little is known about the specific factors that may influence behaviour change during this crucial time. Therefore, we conducted an in-depth exploration of the socioecological influences impacting the diagnostic experience and self-management practices following an MS diagnosis.
We followed a qualitative study design using a phenomenological approach to explore the lived experiences of people newly diagnosed with MS. Analysis was conducted via an iterative process, starting with deductive open coding to map onto the socioecological model, followed by inductive focused coding to extract key themes from participants' reported experiences.
Eight participants diagnosed with MS within the past 12 months were interviewed. Four themes were reported across the MS journey, reflecting the different levels of the socioecological model: (1) taking control of a new diagnosis to retain a sense of personal identity-individual level; (2) grief and acceptance guided by community-social connection, community and social environment; (3) practical management of MS in the wider society-policy and government regulation; and (4) global events that greatly upheave the MS journey-natural disasters and societal conflicts, such as a pandemic. These themes highlighted the complex interrelationship between socioecological factors and self-management abilities in people living with MS.
The diagnostic experience of those with MS is highly complex. Although it varies for each person living with MS, there are shared experiences that often reflect a common cycle of grief. An MS diagnosis provides an opportunity for self-rediscovery, which can both influence and be influenced by socioecological factors. The social and technical nature of self-managing MS strongly shapes the diagnostic experience, underpinning many aspects of daily living, social interaction and physical and psychological well-being.
The research team worked closely with an MS-specific consumer panel for the study design. This project was raised with this group, and preliminary results were shared at a national conference for MS during a lived-experience consumer stream to gain additional insights.
多发性硬化症(MS)的新诊断患者通常会寻求“与健康相关”的行为改变,以控制自己的诊断。然而,人们对可能在这一关键时期影响行为改变的具体因素知之甚少。因此,我们深入探讨了影响 MS 诊断后社会生态影响诊断体验和自我管理实践的因素。
我们采用现象学方法进行了一项定性研究设计,以探索新诊断为 MS 的人的生活经历。通过迭代过程进行分析,首先进行演绎开放式编码,以映射到社会生态模型,然后进行归纳聚焦式编码,从参与者报告的经验中提取关键主题。
对过去 12 个月内被诊断为 MS 的 8 名患者进行了访谈。在 MS 旅程中报告了四个主题,反映了社会生态模型的不同层次:(1)控制新诊断以保持个人身份认同——个体层面;(2)社区社会联系、社区和社会环境指导的悲伤和接受;(3)更广泛社会中 MS 的实际管理——政策和政府法规;(4)极大扰乱 MS 旅程的全球事件——自然灾害和社会冲突,如大流行。这些主题突出了 MS 患者的社会生态因素和自我管理能力之间复杂的相互关系。
MS 患者的诊断体验非常复杂。尽管每个患有 MS 的人都有不同的体验,但也有共同的体验,这些体验常常反映出共同的悲伤循环。MS 诊断为自我重新发现提供了机会,这既可以影响也可以受到社会生态因素的影响。管理 MS 的社会和技术性质强烈塑造了诊断体验,支撑着日常生活、社会互动以及身体和心理健康的许多方面。
研究团队在研究设计中与一个特定于 MS 的消费者小组密切合作。该项目是与该小组一起提出的,并在 MS 全国会议期间的一个现场体验消费者专题讨论会分享了初步结果,以获得更多的见解。