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针对患有长期慢性病的儿童和青少年的定制化家庭数字护理管理应用程序的理想组件:一项定性探索。

Desirable Components for a Customized, Home-Based, Digital Care-Management App for Children and Young People With Long-Term, Chronic Conditions: A Qualitative Exploration.

作者信息

Nightingale Ruth, Hall Andrew, Gelder Carole, Friedl Simone, Brennan Eileen, Swallow Veronica

机构信息

Great Ormond Street Hospital for Children, NHS Foundation Trust, London, United Kingdom.

School of Healthcare, University of Leeds, Leeds, United Kingdom.

出版信息

J Med Internet Res. 2017 Jul 4;19(7):e235. doi: 10.2196/jmir.7760.

Abstract

BACKGROUND

Mobile apps for mobile phones and tablet devices are widely used by children and young people aged 0-18 years with long-term health conditions, such as chronic kidney disease (CKD), and their healthy peers for social networking or gaming. They are also poised to become a major source of health guidance. However, app development processes that are coproduced, rigorously developed, and evaluated to provide tailored, condition-specific, practical advice on day-to-day care management are seldom systematic or sufficiently described to enable replication. Furthermore, attempts to extrapolate to the real world are hampered by a poor understanding of the effects of key elements of app components. Therefore, effective and cost-effective novel, digital apps that will effectively and safely support care management are critical and timely. To inform development of such an app for children with CKD, a user requirements-gathering exercise was first needed.

OBJECTIVE

To explore the views of children with CKD, their parents, and health care professionals to inform future development of a child-focused, care-management app.

METHODS

Using age- and developmentally appropriate methods, we interviewed 36 participants: 5-10-year-olds (n=6), 11-14-year-olds (n=6), 15-18-year-olds (n=5), mothers (n=10), fathers (n=2), and health care professionals (n=7). Data were analyzed using Framework Analysis and behavior change theories.

RESULTS

Of the 27 interviews, 19 (70%) interviews were individual and 8 (30%) were joint-5 out of 8 (63%) joint interviews were with a child or young person and their parent, 1 out of 8 (13%) were with a child and both parents, and 2 out of 8 (25%) were with 2 professionals. Three key themes emerged to inform development of a software requirement specification for a future home-based, digital care-management app intervention: (1) Gaps in current online information and support, (2) Difficulties experienced by children with a long-term condition, and (3) Suggestions for a digital care-management app. Reported gaps included the fact that current online information is not usually appropriate for children as it is "dry" and "boring," could be "scary," and was either hard to understand or not relevant to individuals' circumstances. For children, searching online was much less accessible than using a professional-endorsed mobile app. Children also reported difficulty explaining their condition to others, maintaining treatment adherence, coping with feeling isolated, and with trying to live a "normal" life. There was recognition that a developmentally appropriate, CKD-specific app could support the process of explaining the condition to healthy peers, reducing isolation, adhering to care-management plans, and living a "normal" life. Participants recommended a range of media and content to include in a tailored, interactive, age- and developmentally appropriate app. For example, the user would be able to enter their age and diagnosis so that only age-appropriate and condition-specific content is displayed.

CONCLUSIONS

Future development of a digital app that meets the identified information and support needs and preferences of children with CKD will maximize its utility, thereby augmenting CKD caregiving and optimizing outcomes.

摘要

背景

手机和平板设备上的移动应用程序被患有慢性疾病(如慢性肾病,CKD)的0至18岁儿童和年轻人及其健康的同龄人广泛用于社交网络或游戏。它们也有望成为健康指导的主要来源。然而,共同制作、严格开发和评估以提供关于日常护理管理的量身定制、特定病情实用建议的应用程序开发过程很少是系统的,也没有得到充分描述以实现复制。此外,由于对应用程序组件关键要素的影响了解不足,将其推广到现实世界的尝试受到阻碍。因此,有效且具有成本效益的新型数字应用程序对于有效且安全地支持护理管理至关重要且迫在眉睫。为了为开发这样一款针对CKD儿童的应用程序提供信息,首先需要进行一次用户需求收集活动。

目的

探讨CKD儿童、他们的父母以及医疗保健专业人员的观点,以为未来以儿童为中心的护理管理应用程序的开发提供信息。

方法

我们采用适合年龄和发育阶段的方法,采访了36名参与者:5至10岁儿童(n=6)、11至14岁儿童(n=6)、15至18岁儿童(n=5)、母亲(n=10)、父亲(n=2)以及医疗保健专业人员(n=7)。使用框架分析法和行为改变理论对数据进行了分析。

结果

在27次访谈中,19次(70%)是单独访谈,8次(30%)是联合访谈——8次联合访谈中有5次(63%)是与儿童或年轻人及其父母进行的,8次中有1次(13%)是与儿童及其父母双方进行的,8次中有2次(25%)是与两名专业人员进行的。出现了三个关键主题,为未来基于家庭的数字护理管理应用程序干预的软件需求规范的制定提供信息:(1)当前在线信息和支持方面的差距,(2)患有长期疾病的儿童所经历的困难,(3)对数字护理管理应用程序的建议。报告的差距包括当前在线信息通常不适合儿童,因为它“枯燥”且“无聊”,可能“吓人”,要么难以理解,要么与个人情况无关。对于儿童来说,在线搜索比使用专业认可的移动应用程序要难得多。儿童还报告说,向他人解释自己的病情、坚持治疗、应对孤独感以及努力过“正常”生活都有困难。人们认识到,一款适合发育阶段、针对CKD的应用程序可以支持向健康同龄人解释病情、减少孤独感、坚持护理管理计划以及过“正常”生活的过程。参与者建议在一款量身定制、互动、适合年龄和发育阶段的应用程序中纳入一系列媒体和内容。例如,用户将能够输入自己的年龄和诊断信息,以便只显示适合年龄且针对病情的内容。

结论

开发一款满足已确定的CKD儿童信息、支持需求和偏好的数字应用程序,将使其效用最大化,从而增强CKD护理并优化结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8055/5516103/46d681bd982f/jmir_v19i7e235_fig1.jpg

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