health behavior change

健康行为改变
  • 文章类型: Clinical Trial
    非传染性疾病的流行,比如糖尿病和心血管疾病,在低收入和中等收入国家(LMICs)正在上升。健康行为改变(HBC)干预措施,如广泛使用的糖尿病预防计划(DPP)可有效降低慢性病风险,但尚未适应LMIC。利用移动健康(mHealth)技术(如短信(SMS))来增强这些干预措施的覆盖范围和参与者的参与具有巨大的前景。然而,我们缺乏以证据为依据的方法来指导SMS的整合,以支持LMIC背景下的HBC干预.为了解决这个差距,我们将mHealth文献中的指导与专业知识和第一手经验相结合,为构建和实施SMS系统以支持LMIC中的HBC编程制定了具体的开发步骤.具体来说,我们通过描述我们在设计和交付SMS系统以支持在南非交付的文化适应的DPP方面的经验,提供了每个开发步骤的真实示例。我们概述了八个关键的SMS开发步骤,包括:1)确定SMS是否合适;2)开发系统架构和编程;3)开发基于理论的消息;4)开发SMS技术;5)解决国际SMS交付;6)测试;7)系统培训和技术支持;以及8)成本考虑。我们讨论了经验教训和可提取的原则,这些原则可能对在类似LMIC环境中工作的其他mHealth和HBC研究人员有用。临床试验注册Clinicaltrials.gov,NCT03342274。2017年11月10日注册
    The prevalence of non-communicable diseases, such as diabetes and cardiovascular disease, is rising in low- and middle-income countries (LMICs). Health behavior change (HBC) interventions such as the widely used Diabetes Prevention Program (DPP) are effective at reducing chronic disease risk, but have not been adapted for LMICs. Leveraging mobile health (mHealth) technology such as text messaging (SMS) to enhance reach and participant engagement with these interventions has great promise, yet we lack evidence-informed approaches to guide the integration of SMS specifically to support HBC interventions in LMIC contexts. To address this gap, we integrated guidance from the mHealth literature with expertise and first-hand experience to establish specific development steps for building and implementing SMS systems to support HBC programming in LMICs. Specifically, we provide real-world examples of each development step by describing our experience in designing and delivering an SMS system to support a culturally-adapted DPP designed for delivery in South Africa. We outline eight key SMS development steps, including: 1) determining if SMS is appropriate; 2) developing system architecture and programming; 3) developing theory-based messages; 4) developing SMS technology; 5) addressing international SMS delivery; 6) testing; 7) system training and technical support; and 8) cost considerations. We discuss lessons learned and extractable principles that may be of use to other mHealth and HBC researchers working in similar LMIC contexts.Trial registration Clinicaltrials.gov, NCT03342274 . Registered 10 November 2017.
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  • 文章类型: Journal Article
    需要规范研究干预措施中的健康行为变化(BC)内容,以推进BC科学。其实施,和传播。我们分析了最小的潜在活性BC成分的类型和剂量以及旨在在正在进行的老年人身体活动优化试验中提供的相关行为处方(ReadySteady3.0[RS3])。我们将BC类型定义为行为改变技术(BCT)和行为处方。我们的协议将BCT分类编码过程与BCT角色(主要或次要)集成在一起,当相关时,与行为处方的联系。主要的BCT靶向理论作用机制,而辅助BCT支持主要BCT交付。行为处方代表参与者被鼓励对RS3中的每个主要BCT做什么(确定,实践,implement).我们评估了持续时间的剂量参数,频率,以及每个BCT和处方中的数量。结果提供了一个深入的目录,具有12个主要BCT的多维内容规范,每个由2-7个辅助BCT支持,剂量范围从2到8周,1到8个联系人,5到451分钟.花在行为处方上的时间各不相同:确定(1到41),实践(5至315),并实现(0到38)。结果可以用不同的方式组织和总结(例如,按内容组成),以加强未来对RS3保真度和干预措施细化的评估。结果突出了早期的潜在好处,综合的方法来分析BC的内容和框架的问题如何这些信息可能会被纳入和传播报告的研究成果。
    本案例研究的重点是评估仍在开发中的干预措施中有哪些行为变化内容以及有多少行为变化内容-通过整合现有的对行为变化技术进行分类的框架,剂量,和行为处方。调查结果提供了第一套可用于收集的程序,编码,并分析代表干预中行为改变技术类型的数据,他们的持续时间,频率,和金额,以及他们与参与者被要求做什么的联系。将这些程序应用于正在进行的研究(ReadySteady3.0)中的方案和材料,干预中最小的潜在活跃行为改变成分的多维目录,包括行为改变技术,预期用途,和预期剂量。调查结果还展示了如何以各种方式总结和组织这些信息,以加强保真度评估和未来干预措施的发展。研究人员可以使用和调整这些新程序来报告个人干预研究中的行为变化内容。研究结果还强调了早期的潜在好处,综合方法来分析行为变化的内容和框架的问题,这些信息可能如何被纳入和传播与报告研究成果。
    Specifications of what and how much health behavior change (BC) content within research interventions are needed to advance BC science, its implementation, and dissemination. We analyzed the types and dosages of the smallest potentially active BC ingredients and associated behavioral prescriptions intended to be delivered in an ongoing physical activity optimization trial for older adults (Ready Steady 3.0 [RS3]). We defined BC types as behavior change techniques (BCT) and behavioral prescriptions. Our protocol integrated the BCT Taxonomy coding procedures with BCT roles (primary or secondary) and, when relevant, linkages to behavioral prescriptions. Primary BCTs targeted theoretical mechanisms of action, whereas secondary BCTs supported primary BCT delivery. Behavioral prescriptions represented what participants were encouraged to do with each primary BCT in RS3 (ascertain, practice, implement). We assessed dosage parameters of duration, frequency, and amount in each BCT and prescription. Results provided a catalog of in-depth, multidimensional content specifications with 12 primary BCTs, each supported by 2-7 secondary BCTs, with dosages ranging from 2 to 8 weeks, 1 to 8 contacts, and 5 to 451 minutes. Minutes spent on behavioral prescriptions varied: ascertain (1 to 41), practice (5 to 315), and implement (0 to 38). Results can be organized and summarized in varied ways (e.g., by content component) to strengthen future assessments of RS3 fidelity and intervention refinement. Results highlight potential benefits of this early, integrated approach to analyzing BC content and frames questions about how such information might be incorporated and disseminated with reporting research outcomes.
    The focus of this case study was to assess what and how much behavior change content was within an intervention still under development—by integrating existing frameworks for classifying behavior change techniques, dosages, and behavioral prescriptions. Findings provide the first set of procedures available for collecting, coding, and analyzing data representing the types of behavior change techniques in an intervention, their durations, frequencies, and amounts, and their linkages to what participants are asked to do. Applying these procedures to the protocol and materials in an ongoing study (Ready Steady 3.0) yielded a detailed, multidimensional catalog of the smallest potentially active behavior change ingredients in its intervention, including behavior change techniques, intended uses, and intended dosages. Findings also showcased how this information can be summarized and organized in various ways to strengthen fidelity evaluations and future intervention development. Researchers can use and adapt these new procedures for reporting behavior change content within individual intervention studies. Findings also highlight the potential benefits of this early, integrated approach to analyzing behavior change content and frame questions about how such information might be incorporated and disseminated with reporting research outcomes.
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  • 文章类型: Journal Article
    Addressing patient health and care behaviors that underlie much of chronic disease continues to challenge providers, medical practices, health systems, and insurers. Improving health and care as described by the Quadruple Aim requires innovation at the front lines of clinical care: the doctor-patient interaction and office practice. This article describes the use of Lean Six Sigma in a quality improvement (QI) effort to design an effective and scalable method for physicians to prescribe health coaching for healthy behaviors in a primary care medical home within a large integrated delivery and financing system. Building on the national Agency for Healthcare Research and Quality and Robert Wood Johnson Foundation-funded Prescription for Health multisite demonstration, this QI case study provides important lessons for transforming patient-physician-practice support systems to better address lifestyle and care management challenges critical to producing better outcomes.
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  • 文章类型: Journal Article
    Background: Smoking continues to be a public health problem worldwide. Smoking and tobacco use are associated with cardiovascular diseases that include coronary heart disease, atherosclerosis, cerebrovascular disease, and abdominal aortic aneurysm. Programs for quitting smoking have played a significant role in reduction of smoking in the United States. The smoking cessation interventions include counseling, nicotine replacement therapy, buproprion therapy, and varenicline therapy. The success rates with each of these approaches vary with clear need for improvement. Moreover, there is a need for a robust theory that can guide smoking cessation counseling interventions and increase the success rates. A fourth generation approach using multi-theory model (MTM) of health behavior change is introduced in this article for smoking cessation. An approach for developing and evaluating an intervention for smoking cessation is presented along with a measurement tool. Methods: A literature review reifying the MTM of health behavior change for smoking cessation has been presented. An instrument designed to measure constructs of MTM and associated smoking cessation behavior has been developed. Results: The instrument developed is available for validation, reliability and prediction study pertaining to smoking cessation. The intervention is available for testing in a randomized control trial involving smokers. Conclusion: MTM is a robust theory that holds promise for testing and application to smoking cessation.
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