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使用拟人化虚拟助手软件开发一种复杂干预措施,以提高老年人对抗糖尿病药物的依从性。

Development of a Complex Intervention to Improve Adherence to Antidiabetic Medication in Older People Using an Anthropomorphic Virtual Assistant Software.

作者信息

Félix Isa Brito, Guerreiro Mara Pereira, Cavaco Afonso, Cláudio Ana Paula, Mendes Anabela, Balsa João, Carmo Maria Beatriz, Pimenta Nuno, Henriques Adriana

机构信息

Unidade de Investigação e Desenvolvimento em Enfermagem (UI&DE), Lisbon Nursing School, Lisbon, Portugal.

Centro de Investigação Interdisciplinar Egas Moniz (CiiEM), Instituto Universitário Egas Moniz, Monte de Caparica, Portugal.

出版信息

Front Pharmacol. 2019 Jun 21;10:680. doi: 10.3389/fphar.2019.00680. eCollection 2019.

DOI:10.3389/fphar.2019.00680
PMID:31281256
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6597679/
Abstract

Improving adherence to antidiabetic medication is crucial, resulting in improved health outcomes, cost reduction, and minimization of waste. A lack of underlying theory in existing interventions may explain the limited success in sustaining behavior change. This paper describes the development of a theory and evidence-based complex intervention to improve adherence to oral antidiabetics in older people a software prototype with an anthropomorphic virtual assistant. The Behavior Change Wheel (BCW) was used to develop a theoretical understanding of the change process, corresponding to the first phase of the Medical Research Council Framework for developing and evaluating complex interventions. At the BCW core is a model of human behavior (COM-B), which posits that human behavior (B) results from the interaction between capabilities (C), opportunities (O), and motivation (M). Literature-derived medication adherence determinants were mapped onto COM-B components. Then, intervention functions (IFs) were selected employing the APEASE criteria. Finally, standardized behavior change techniques (BCTs) were chosen based on their suitability and their effectiveness on medication adherence trials. The prototype was developed for android devices; its core was implemented in Unity3D, using a female 3D virtual assistant, named Vitória. Two COM-B components were identified as main targets for behavior change-psychological capability and reflective motivation; these were linked with four IFs-education, persuasion, enablement, and environmental restructuring. Eleven BCTs were, in turn, linked with the IFs. An example of a BCT is "problem solving"; it requires users to pinpoint factors influencing non-adherence and subsequently offers strategies to achieve the desired behavior. BCTs were operationalized into the dialogues with Vitória and into supplementary software features. Vitória communicates with users verbally and non-verbally, expressing emotions. Input options consist of buttons or recording values, such as medication taken. The present approach enabled us to derive the most appropriate BCTs for our intervention. The use of an explicit bundle of BCTs, often overlooked in interventions promoting medication adherence, is expected to maximize effectiveness and facilitates replication. The first prototype is being refined with users and health professionals' contributions. Future work includes subjecting the prototype to usability tests and a feasibility trial.

摘要

提高抗糖尿病药物的依从性至关重要,这会带来更好的健康结果、降低成本并减少浪费。现有干预措施缺乏基础理论可能解释了在维持行为改变方面取得的成功有限。本文描述了一种基于理论和证据的复杂干预措施的开发,以提高老年人对口服抗糖尿病药物的依从性——一个带有拟人化虚拟助手的软件原型。行为改变轮(BCW)被用于对改变过程形成理论理解,这对应于医学研究理事会开发和评估复杂干预措施框架的第一阶段。BCW的核心是一个人类行为模型(COM-B),该模型假定人类行为(B)源于能力(C)、机会(O)和动机(M)之间的相互作用。从文献中得出的药物依从性决定因素被映射到COM-B的各个组成部分上。然后,采用APEASE标准选择干预功能(IFs)。最后,根据标准化行为改变技术(BCTs)对药物依从性试验的适用性和有效性来选择它们。该原型是为安卓设备开发的;其核心在Unity3D中实现,使用了一个名为维多利亚的女性3D虚拟助手。确定了两个COM-B组成部分作为行为改变的主要目标——心理能力和反思动机;这些与四个IFs——教育、劝说、赋能和环境重构相联系。反过来,11个BCTs与这些IFs相联系。一个BCT的例子是“解决问题”;它要求用户找出影响不依从的因素,随后提供实现期望行为的策略。BCTs被落实到与维多利亚的对话以及补充软件功能中。维多利亚通过口头和非口头方式与用户交流,表达情感。输入选项包括按钮或记录值,如所服用的药物。目前的方法使我们能够为我们的干预措施得出最合适的BCTs。在促进药物依从性的干预措施中经常被忽视的明确的BCTs组合的使用,有望使有效性最大化并便于复制。第一个原型正在根据用户和健康专业人员的建议进行完善。未来的工作包括对该原型进行可用性测试和可行性试验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08fb/6597679/b9ee3fc68ce0/fphar-10-00680-g005.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08fb/6597679/d68a9c287172/fphar-10-00680-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08fb/6597679/20441307a4b4/fphar-10-00680-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08fb/6597679/08afbf6ad604/fphar-10-00680-g003.jpg
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