Patient Centered mobile Health TECHnology Enabled Atrial Fibrillation Management (mTECH Afib): A Pilot Randomized Controlled Trial.

IF 8 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Nino Isakadze, Natalie A Horstman, Jie Ding, Courtney Eddy, Stephney Blair, Chang H Kim, Luu V Pham, Francoise A Marvel, Erin M Spaulding, Mansi Nimbalkar, Erin D Michos, Jeffrey Sham, Patrick Dunn, Joseph E Marine, Hugh Calkins, Seth S Martin, David Spragg
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引用次数: 0

Abstract

Background: Digital health technologies provide a scalable, efficient approach to implementing guideline-recommended risk factor modification in the care of patients with atrial fibrillation (AF).

Objectives: This study aimed to evaluate the feasibility of a 12-week, multicomponent, virtual AF management program using a smartphone application, connected devices, and virtual coaching calls for risk factor modification.

Methods: Patients with AF were enrolled from outpatient clinics. Patients were randomized in a 1:1 ratio to either usual care only or the virtual program. The study objectives were to assess feasibility, with the goal of achieving at least 60% participant retention at 12 weeks, intervention engagement, and participant satisfaction.

Results: Among 61 patients enrolled (76% of those approached), the mean age was 65 ± 8 years, and 36% were women. A total of 89% of all participants were retained by 12-week follow-up. In the intervention group, at 12-weeks, 88% continued using the smartphone application, 73% continued participation in virtual coaching calls, and 80% reported being satisfied with the program.

Conclusions: The mTECH Afib (Patient Centered mobile health TECHnology Enabled Atrial Fibrillation Management) trial demonstrates feasibility of conducting a randomized controlled trial using an innovative digital health technology-enabled intervention with broad patient engagement and acceptance of the program components. Large-scale clinical trials powered for health outcomes will be necessary to establish intervention efficacy.

以患者为中心的移动医疗技术支持心房颤动管理(mTECH Afib):一项试点随机对照试验。
背景:数字健康技术提供了一种可扩展的、有效的方法来实施指南推荐的房颤(AF)患者护理中的危险因素修改。目的:本研究旨在评估一项为期12周、多组件的虚拟房颤管理计划的可行性,该计划使用智能手机应用程序、连接设备和虚拟教练电话进行风险因素修改。方法:从门诊纳入房颤患者。患者按1:1的比例随机分为常规治疗组和虚拟治疗组。研究目的是评估可行性,目标是在12周时达到至少60%的参与者保留率、干预参与度和参与者满意度。结果:入组的61例患者(76%)平均年龄为65±8岁,36%为女性。在12周的随访中,总共有89%的参与者被保留下来。在干预组,在12周时,88%的人继续使用智能手机应用程序,73%的人继续参加虚拟教练电话,80%的人表示对该计划感到满意。结论:mTECH Afib(以患者为中心的移动健康技术支持的房颤管理)试验证明了采用创新的数字健康技术支持的干预措施进行随机对照试验的可行性,该干预措施具有广泛的患者参与和对计划组成部分的接受度。为健康结果提供动力的大规模临床试验将是确定干预效果的必要条件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
JACC. Clinical electrophysiology
JACC. Clinical electrophysiology CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
10.30
自引率
5.70%
发文量
250
期刊介绍: JACC: Clinical Electrophysiology is one of a family of specialist journals launched by the renowned Journal of the American College of Cardiology (JACC). It encompasses all aspects of the epidemiology, pathogenesis, diagnosis and treatment of cardiac arrhythmias. Submissions of original research and state-of-the-art reviews from cardiology, cardiovascular surgery, neurology, outcomes research, and related fields are encouraged. Experimental and preclinical work that directly relates to diagnostic or therapeutic interventions are also encouraged. In general, case reports will not be considered for publication.
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