首页> 美国卫生研究院文献>Current Controlled Trials in Cardiovascular Medicine >Comparing satisfaction with a participatory driven web-application and a standard website for patients with low back pain: a study protocol for a randomised controlled trial (part of the ADVIN Back Trial)
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Comparing satisfaction with a participatory driven web-application and a standard website for patients with low back pain: a study protocol for a randomised controlled trial (part of the ADVIN Back Trial)

机译:通过参与性驱动的Web应用程序和腰痛患者的标准网站来比较满意度:一项针对随机对照试验的研究方案(ADVIN背部试验的一部分)

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摘要

BackgroundLow back pain (LBP) is the most common musculoskeletal disorder and a leading cause of disability worldwide. It impacts daily life and work capacity and is the most common reason for consulting a general practitioner (GP). According to international guidelines, information, reassurance, and advice are key components in the management of people with LBP; however, the consultation time available in general practice for each patient is often limited. Therefore, new methods to support the delivery of information and advice are needed and online technologies provide new opportunities to extend the consultation beyond the GP’s office. However, it is not known whether GPs and people consulting their GP because of LBP will accept online technologies as part of the consultation. By involving patients in the development of online information, we may produce more user-friendly content and design, and improve patient acceptance and usage, optimising satisfaction and clinical outcomes. The purpose is to study satisfaction in people consulting their GP with LBP depending on whether they are randomised to receive supporting information through a new participant-driven web application or a standard reference website containing guideline-based information on LBP. It is hypothesised that patients offered information in a new web application will be more satisfied with the online information after 12 weeks compared to patients allocated to a standard website.
机译:背景下腰痛(LBP)是最常见的肌肉骨骼疾病,也是全球致残的主要原因。它会影响日常生活和工作能力,并且是咨询全科医生(GP)的最常见原因。根据国际准则,信息,保证和咨询是LBP患者管理的关键组成部分。但是,通常情况下,每个患者的咨询时间通常很有限。因此,需要新的方法来支持信息和建议的传递,并且在线技术为将咨询范围扩展到GP的办公室之外提供了新的机会。但是,尚不知道GP和因LBP而咨询其GP的人员是否会接受在线技术作为咨询的一部分。通过让患者参与在线信息的开发,我们可能会产生更人性化的内容和设计,并提高患者的接受度和使用率,优化满意度和临床结果。目的是研究通过LBP向GP咨询其GP的人们的满意度,具体取决于他们是通过新的参与者驱动的Web应用程序还是包含有关LBP的基于指南信息的标准参考网站被随机分配以接收支持信息。假设与分配到标准网站的患者相比,在新的Web应用程序中提供信息的患者在12周后会对在线信息更加满意。

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