Participatory design of an infographic to help support the care of people living with complex regional pain syndrome.

IF 1.3 Q4 CLINICAL NEUROLOGY British Journal of Pain Pub Date : 2023-12-01 Epub Date: 2023-07-28 DOI:10.1177/20494637231190587
Darren Beales, Yi Ki Ho, James Lewin, Bianca Wen-Qi Loh, Amirah Binte Yusof, Sharon Grieve, Sonia Ranelli, David Holthouse, Tim Mitchell, Helen Slater
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Abstract

Background: Complex regional pain syndrome (CRPS) can be a debilitating pain condition with enduring physical, psychological and social impacts. CRPS is often poorly understood by healthcare professionals and management needs to be tailored to each individual's presentation. People with lived experience express difficulty in accessing reliable and meaningful information about the condition. This study aimed to co-create a trustworthy infographic to share information about the lived experience of CRPS.

Methods: We adopted a seven-phase, iterative, participatory methodology to co-create the infographic. Potential infographic content was obtained from qualitative work investigating the lived experience of CRPS. Online consumer engagement (people with doctor diagnosed CRPS/their family, n=20) was used to prioritise content to be included in the infographic and then potential designs were sourced. The research team narrowed the selections down to two designs which were presented to consumers online for final selection (n=25) and refinement (n=34).

Results: An infographic for understanding the lived experience of CRPS was completed using participatory design, providing a resource aligned to the needs of people with this condition. Using the Patient Education Materials Assessment Tool, the final infographic rated highly for understandability (92%) and participants indicated significant willingness to share this infographic with others (93%).

Conclusion: A process of participatory design was an effective and efficient process for translation of evidence gathered from qualitative research into a trustworthy resource for people with CRPS and their support people.

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参与设计的信息图表,以帮助支持照顾人生活与复杂的区域疼痛综合征
复杂区域疼痛综合征(CRPS)可能是一种使人衰弱的疼痛状况,具有持久的身体、心理和社会影响。CRPS通常不被医疗专业人员所理解,管理需要根据每个人的表现进行定制。有生活经验的人表示很难获得有关这种情况的可靠和有意义的信息。本研究旨在共同创建一个值得信赖的信息图,以分享有关CRPS生活体验的信息。我们采用了一种七阶段、迭代、参与式的方法来共同创建信息图。潜在的信息图表内容是从调查CRPS生活体验的定性工作中获得的。在线消费者参与(医生诊断为CRPS的人/他们的家人,n=20)被用于优先考虑信息图中包含的内容,然后寻找潜在的设计。研究团队将选择范围缩小到两种设计,并在网上提交给消费者进行最终选择(n=25)和改进(n=34)。使用参与式设计完成了一张了解CRPS生活体验的信息图,提供了一种符合这种情况下人们需求的资源。使用患者教育材料评估工具,最终信息图的可理解性得到了很高的评价(92%),参与者表示非常愿意与他人分享此信息图(93%)。参与式设计过程是一个有效和高效的过程,可以将从定性研究中收集的证据转化为CRPS患者及其支持人员的可靠资源。
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来源期刊
British Journal of Pain
British Journal of Pain CLINICAL NEUROLOGY-
CiteScore
3.20
自引率
11.10%
发文量
42
期刊介绍: British Journal of Pain is a peer-reviewed quarterly British journal with an international multidisciplinary Editorial Board. The journal publishes original research and reviews on all major aspects of pain and pain management. Reviews reflect the body of evidence of the topic and are suitable for a multidisciplinary readership. Where empirical evidence is lacking, the reviews reflect the generally held opinions of experts in the field. The Journal has broadened its scope and has become a forum for publishing primary research together with brief reports related to pain and pain interventions. Submissions from all over the world have been published and are welcome. Official journal of the British Pain Society.
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