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Promoting Physical Activity With Self-Tracking and Mobile-Based Coaching for Cardiac Surgery Patients During the Discharge–Rehabilitation Gap: Protocol for a Randomized Controlled Trial

机译:在排放康复差距期间促进与自动跟踪和基于移动的辅导的体育活动:随机对照试验的议定书

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Background Home-based cardiac rehabilitations (CRs) with digital technologies have been researched and implemented to replace, augment, and complement traditional center-based CR in recent years with considerable success. One problem that technology-enhanced home-based CR can potentially address is the gap between cardiac interventions and formal CR programs. In the Netherlands and some other countries (eg, Australia), patients after cardiac interventions stay at home for 3-4 weeks without much support from their physicians, and often engage in very little physical activity (PA). A home-based exercise program enabled by digital technologies may help patients to better prepare for the later center-based CR programs, potentially increasing the uptake rate of those programs. Objective In a randomized controlled trial (RCT), we will evaluate the effectiveness of a home-based walking exercise program enhanced by self-tracking and mobile-based coaching (treatment condition), comparing it with a version of the same program without these technologies (control condition). The added value of the digital technologies is justified if patients in the treatment group walk more steps on average (primary outcome) and show better physical fitness in a bicycle ergometer test and higher self-efficacy toward PA (secondary outcomes). Methods Based on a power analysis, we will recruit 100 cardiac patients and assign them evenly to the 2 parallel groups. Eligible patients are those who are scheduled in the postanesthesia care unit, know the Dutch language, have basic literacy of using smartphones, and are without medical conditions that may increase risks associated with PA. In a face-to-face meeting with a nurse practitioner, all patients are prescribed a 3-week exercise program at home (2 walking exercises per day with increasing duration), based on national and international guidelines and tailored to their physical conditions after cardiac intervention. Their physical activities (daily steps) will be measured by the Axivity AX3 accelerometer worn at hip position. Patients in the treatment group will also be supported by a Neo Health One self-tracking device and a mobile platform called Heart Angel, through which they are monitored and coached by their nurses. After the study, all patients will perform a bicycle ergometer test and return the devices within 1 week. In addition, 5 questionnaires will be sent to the patients by emails to assess their self-efficacy toward PA and other psychological states for exploratory analyses (at discharge, at the end of each monitoring week, and 1 week after the study). To minimize bias, the randomization procedure will be performed after introducing the exercise program, so the nurse practitioners are blind to the experimental conditions until that point. Results The study protocol has been approved by the Medical Research Ethics Committees United on February 26, 2018 (NL 62142.100.17/R17.51). By the end of 2018, we completed a small pilot study with 8 patients and the results based on interviews and app usage data suggest that a larger clinical trial with the targeted population is feasible. We expect to complete the RCT by the end of 2021, and statistical analyses will follow. Conclusions Results of the RCT will help us to test the hypothesized benefits of self-tracking and mobile-based coaching for cardiac patients in home-based exercise programs during the discharge–rehabilitation gap. If the results are positive, cost-effectiveness analysis will be performed based on the insights of the study to inform the translation of the technology-enhanced program to clinical practice. We also note limitations of the trial in the discussion.
机译:近年来,已经研究和实施了具有数字技术的基于家庭的心脏康复(CRS),以取代,增强和补充传统的中心CR,以相当大的成功。技术增强的家庭基于家庭的CR可能会解决一个问题是心脏干预和正式CR计划之间的差距。在荷兰和其他一些国家(例如,澳大利亚),心脏干预后的患者留在家里3-4周,没有太多的支持他们的医生,并且经常从事很少的身体活动(PA)。数字技术支持的基于家庭的锻炼计划可能有助于患者更好地为基于中心的CR计划做好准备,可能会增加这些计划的摄取率。目的在随机对照试验(RCT)中,我们将通过自动跟踪和基于移动的教练(治疗状况)来评估基于家庭的行走运动程序的有效性,将其与没有这些技术的同一节目的版本(控制条件)。如果治疗组中的患者平均地(主要结果)走出更多步骤,并且在自行车测力计测试中表现出更好的身体健康,并且对PA(二次结果)展示了更好的身体健康,则是合理的。方法基于功率分析,我们将招募100名心脏病患者,并将其分配给2个平行组。符合条件的患者是那些定于破旧的护理单位的人,了解荷兰语,具有使用智能手机的基本识字,并且没有医疗条件可能会增加与PA相关的风险。在与护士从业者的面对面会晤中,所有患者在家里规定了3周的运动计划(每天2个行走练习,持续时间增加),基于国家和国际指南,并在心脏病后量身定制干涉。它们的物理活动(每日步骤)将通过在臀部位置佩戴的Axiving Ax3加速度计来测量。治疗组中的患者也将由Neo Health一个自我跟踪装置和一个名为Heart Angel的移动平台支持,他们通过护士监控和执教。研究后,所有患者都将进行自行车测力计测试并在1周内退回设备。此外,5个问卷将通过电子邮件发送给患者,以评估他们对PA和其他心理状态进行探索性分析的自我效力(在每个监测周结束时,研究后1周)。为了最大限度地减少偏差,将在引入锻炼计划后进行随机化程序,因此护士从业者对实验条件盲目,直到该点。结果研究议定书已由医学研究伦理委员会于2018年2月26日核准(NL 62142.100.17 / R17.51)。截至2018年底,我们完成了8名患者的小型试点研究,并根据访谈和应用程序使用数据表明,具有目标人口的更大临床试验是可行的。我们希望在2021年底之前完成RCT,并将遵循统计分析。结论RCT的结果将有助于我们测试在排放康复差距期间,在国基运动计划中测试心脏患者的自我跟踪和移动的教练的假设益处。如果结果是阳性的,将基于研究的见解来进行成本效益分析,以便向临床实践提供技术增强计划的翻译。我们还注意到讨论中试验的限制。

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