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A Co-Designed Social Media Intervention to Satisfy Information Needs and Improve Outcomes of Patients With Chronic Kidney Disease: Longitudinal Study

机译:共同设计的社交媒体干预,以满足信息需求和改善慢性肾病患者的结果:纵向研究

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Background: The number of people living with a long-term condition is increasing worldwide. Social media offers opportunities for patients to exchange information and experiences with others with the same condition, potentially leading to better self-management and improved patient outcomes, at minimal costs to health service providers. Objective: This paper describes how an online network with a range of social media platforms was created, with the help of a group of patients with chronic kidney disease and specialist professionals. The project considered whether information needs and health-related and social outcomes were met. Methods: We performed a longitudinal in-depth evaluation of the creation of the moderated network, observation of the use of the platforms, self-efficacy surveys (at baseline and 6 months), and semistructured interviews (at baseline and 6 months). Results: A total of 15 patients and professionals participated in the co-design of the network (hub), which was initially launched with 50 patients. Several platforms were needed to engage patients at different levels and encourage generation of information, with the support of moderators. In addition, 14 separate patients participated in the evaluation. Satisfaction of information needs through social engagement improved self-efficacy (n=13) with better self-care and management of illness. Social outcomes included seeking employment and an increase in social capital. Conclusions: An online network (hub) with several social media platforms helped patients with chronic kidney disease manage their condition. Careful co-designing with users resulted in a sustainable network with wider applicability across health and social care.
机译:背景:生活在长期条件下的人数正在全世界增加。社交媒体为患者提供交换信息和经验的机会,以相同的条件交换信息和经验,可能导致更好的自我管理和改进的患者结果,以最低的卫生服务提供商。目的:介绍如何在一组慢性肾病和专业专业人员患者的帮助下创建具有一系列社交媒体平台的在线网络。该项目审议了是否满足了信息需求和与健康相关和社会成果。方法:我们对创建纵向进行了深入的评估,对众所周知的网络,观察平台的使用,自我效能调查(在基线和6个月)以及半系统的访谈(基线和6个月)。结果:共有15名患者和专业人士参加了网络(集线器)的共同设计,最初用50名患者发射。需要在不同层面的患者中接触几个平台,并通过主持人的支持,鼓励发电信息。此外,14名单独的患者参加了评估。通过社会参与提高自我效能(n = 13),对信息需求的满意度提高了自我保健和疾病管理。社会成果包括在寻求就业和增加社会资本。结论:具有若干社交媒体平台的在线网络(集线器)帮助慢性肾病患者管理其状况。仔细共同设计与用户导致可持续网络,跨健康和社会护理更广泛的适用性。

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