Development of an internet-delivered program and platform for the treatment of depression and anxiety in patients with ischemic heart disease in eMindYourHeart.

IF 2.5 4区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Informatics for Health & Social Care Pub Date : 2021-06-02 Epub Date: 2021-02-25 DOI:10.1080/17538157.2021.1878185
Thomas Schmidt, Robin Kok, Christina M Andersen, Søren J Skovbakke, Robert Ahm, Uffe Kock Wiil, Lisbeth Frostholm, Susanne S Pedersen
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引用次数: 7

Abstract

To design and evaluate a mental health treatment program and internet-based delivery platform for patients with ischemic heart disease (IHD) attending cardiac rehabilitation with the aim of reducing the risks associated with anxiety and/or depression. Patients diagnosed with IHD and comorbid anxiety and/or depression. Participatory design of treatment program and internet platform through staged inclusion of participants in two groups. Group 1 was enrolled as co-researchers with prolonged engagement in the project. Group 2 participated only in the pilot evaluation workshop. Three patients were included in Group 1, two patients in Group 2. Inclusion of patients proved challenging, but the extended collaboration with co-researchers yielded valuable circumstantial insight and resulted in the design of a novel nine-module treatment program. Additionally, the inclusion of two participant groups helped shape the development of an internet platform based on an open-source content management system. Our grouped participation method contributes with several recommendations and reflections of advantages of this approach. Collaboration with co-researchers helped us gain a deeper understanding of the impact of language on self-perception and potential stigma. Prolonged participation led to a higher level of trust and familiarity, which enabled uncovering of issues otherwise hidden.

eMindYourHeart中缺血性心脏病患者抑郁和焦虑治疗的互联网交付程序和平台的开发。
设计和评估缺血性心脏病(IHD)患者参加心脏康复的心理健康治疗方案和基于互联网的交付平台,旨在降低与焦虑和/或抑郁相关的风险。诊断为IHD并伴有焦虑和/或抑郁的患者。通过分阶段纳入两组参与者,进行治疗方案和互联网平台的参与式设计。第一组被招募为长期参与该项目的共同研究人员。第2组只参加了试点评价讲习班。1组3例,2组2例。纳入患者被证明是具有挑战性的,但与共同研究人员的长期合作产生了宝贵的间接见解,并导致了一个新的九个模块治疗方案的设计。此外,两个参与小组的加入有助于形成基于开源内容管理系统的互联网平台的发展。我们的分组参与方法有助于一些建议和反映这种方法的优势。与共同研究人员的合作帮助我们更深入地了解语言对自我认知和潜在耻辱的影响。长时间的参与导致了更高程度的信任和熟悉,这使得发现原本隐藏的问题成为可能。
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来源期刊
CiteScore
6.10
自引率
4.20%
发文量
21
审稿时长
>12 weeks
期刊介绍: Informatics for Health & Social Care promotes evidence-based informatics as applied to the domain of health and social care. It showcases informatics research and practice within the many and diverse contexts of care; it takes personal information, both its direct and indirect use, as its central focus. The scope of the Journal is broad, encompassing both the properties of care information and the life-cycle of associated information systems. Consideration of the properties of care information will necessarily include the data itself, its representation, structure, and associated processes, as well as the context of its use, highlighting the related communication, computational, cognitive, social and ethical aspects. Consideration of the life-cycle of care information systems includes full range from requirements, specifications, theoretical models and conceptual design through to sustainable implementations, and the valuation of impacts. Empirical evidence experiences related to implementation are particularly welcome. Informatics in Health & Social Care seeks to consolidate and add to the core knowledge within the disciplines of Health and Social Care Informatics. The Journal therefore welcomes scientific papers, case studies and literature reviews. Examples of novel approaches are particularly welcome. Articles might, for example, show how care data is collected and transformed into useful and usable information, how informatics research is translated into practice, how specific results can be generalised, or perhaps provide case studies that facilitate learning from experience.
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