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一项共同设计的社交媒体干预措施,以满足慢性肾病患者的信息需求并改善其治疗效果:纵向研究

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

作者信息

Vasilica Cristina Mihaela, Brettle Alison, Ormandy Paula

机构信息

The University of Salford, School of Health and Society, Salford, United Kingdom.

出版信息

JMIR Form Res. 2020 Jan 27;4(1):e13207. doi: 10.2196/13207.

Abstract

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.

摘要

背景

全球患有长期疾病的人数正在增加。社交媒体为患者提供了与其他患有相同疾病的人交流信息和经验的机会,这可能以最低的医疗服务提供者成本带来更好的自我管理和改善患者预后。

目的

本文描述了如何在一群慢性肾脏病患者和专科专业人员的帮助下创建一个拥有一系列社交媒体平台的在线网络。该项目探讨了信息需求以及与健康相关的和社会的结果是否得到满足。

方法

我们对这个有主持人的网络的创建进行了纵向深入评估,观察了平台的使用情况,进行了自我效能调查(在基线和6个月时)以及半结构化访谈(在基线和6个月时)。

结果

共有15名患者和专业人员参与了网络(中心)的共同设计,该网络最初有50名患者加入。需要几个平台来吸引不同层次的患者并鼓励信息生成,同时有主持人提供支持。此外,14名不同的患者参与了评估。通过社交互动满足信息需求提高了自我效能(n = 13),改善了疾病的自我护理和管理。社会成果包括寻找工作和社会资本的增加。

结论

一个拥有多个社交媒体平台的在线网络(中心)帮助慢性肾脏病患者管理他们的病情。与用户仔细共同设计产生了一个可持续的网络,在健康和社会护理领域具有更广泛的适用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9976/7011121/d4db1e2d6e9c/formative_v4i1e13207_fig1.jpg

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