患者健康参与(PHE)模式对PCI术后急性心肌梗死患者参与康复治疗的影响:随机对照试验研究方案。

IF 2 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Trials Pub Date : 2024-11-22 DOI:10.1186/s13063-024-08643-3
Zixian Liu, Guangfang Zhang, Xiaolei Liang, Dechun Qin
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引用次数: 0

摘要

背景:经皮冠状动脉介入治疗(PCI)后的急性心肌梗死(AMI)患者参与心脏康复的比例较低。虽然现有的康复方法取得了一定的效果,但患者参与运动康复的情况并不理想。患者健康参与(PHE)模式旨在确保患者在认知、情感、行为等各方面提高对运动康复各阶段的参与度。本研究旨在证实,与传统康复模式相比,基于 PHE 模式的康复方法是否能提高急性心肌梗死患者在心脏康复过程中的参与率并增强康复效果:这是一项单中心、双盲、随机对照试验,将招募 128 名患者。接受过心脏康复治疗、术后 LVEF ≥ 40%、Killip 分级 I ~ II、年龄≥ 18 岁的 PCI 术后急性心肌梗死稳定期患者将被纳入研究。排除标准主要是恶性心律失常、急性心力衰竭、充血性心力衰竭以及需要主动脉内球囊反搏的患者。患者将按 1:1 的比例随机分配到干预组(1)和对照组(2)。在研究过程中,医生、康复专家、患者和数据收集人员都将是盲人。一名康复师和一名专业护士将进行心脏康复训练。专科护士将把装有患者信息(第 1 组或第 2 组)的密封袋交给医生。第一组将通过 PHE 模式进行心脏康复治疗,每周三次,为期 3 个月。康复计划将在每个康复阶段进行评估和及时调整。第二组将接受常规心脏康复治疗。两组的康复参与率将在干预 3 个月前后进行评估。主要结果是患者参与康复的程度,次要结果包括患者的一般数据、术后康复指标、心脏康复知识-态度-实践问卷、心血管不良事件和简易情绪量表:我们期望使用 PHE 模式提高急性心肌梗死患者接受 PCI 后的心脏康复参与率和康复效果:该方法可提高患者康复参与率,改善康复效果,并可在医院和康复中心广泛实施:试验注册:ClinicalTrials.gov标识符,ChiCTR2400085276(2024年6月4日2.0版),https://www.chictr.org.cn .试验主办方:山东第二医科大学,潍坊市人民医院:试验主办方:山东第二医科大学,山东潍坊。联系人:秦德春,地址:山东省潍坊市山东第二医科大学:地址:山东潍坊,山东第二医科大学。电子邮件::13562666589@163.com.
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of a patient health engagement (PHE) model on rehabilitation participation in patients with acute myocardial infarction after PCI: a study protocol for a randomized controlled trial.

Background: Participation in cardiac rehabilitation is low in patients with acute myocardial infarction (AMI) after percutaneous coronary intervention (PCI). Although existing rehabilitation methods have achieved certain results, patient participation in exercise rehabilitation is not ideal. The Patient Health Engagement (PHE) model is designed to ensure that patients improve their participation in cognitive, emotional, behavioral, and other aspects in all phases of exercise rehabilitation. The purpose of this study is to confirm whether the rehabilitation method based on the PHE model improves the rate of patient participation and enhances the rehabilitation effect during cardiac rehabilitation in patients with acute myocardial infarction compared with the traditional rehabilitation model.

Methods/design: This is a single-center, double-blind, randomized, controlled trial that will enroll 128 patients. Patients with stable acute myocardial infarction after undergoing PCI who received cardiac rehabilitation and postoperative LVEF ≥ 40%, categorized into Killip class I ~ II and with age ≥ 18 years, will be included in the study. Exclusion criteria are mainly malignant arrhythmias, acute heart failure, congestive heart failure, and patients requiring intra-aortic balloon counterpulsation. Patients will be randomized in a 1:1 ratio to the intervention (1) and control (2) groups. Physicians, rehabilitation specialists, patients, and data collectors will be blinded during the study. A rehabilitator and a specialist nurse will conduct the cardiac rehabilitation. The specialist nurse will hand over the sealed bag containing patient information (group 1 or 2) to the physician. Group 1 will undergo cardiac rehabilitation through the PHE model, three times a week for 3 months. The rehabilitation program will be evaluated and adjusted in time from each period of the rehabilitation. Group 2 will be treated with routine cardiac rehabilitation. The rehabilitation participation rate of the two groups will be evaluated before and after 3 months of intervention. The primary outcome will be the level of patient participation in rehabilitation, and the secondary outcome will include general data of patients, postoperative rehabilitation indicators, cardiac rehabilitation knowledge-attitude-practice questionnaire, cardiovascular adverse events, and a brief mood scale.

Expected outcomes: We expect improved cardiac rehabilitation participation rates and rehabilitation outcomes in patients with acute myocardial infarction after undergoing PCI using the PHE model.

Discussion: This approach may increase patient participation in rehabilitation, improve rehabilitation outcomes, and be widely implemented in hospitals and rehabilitation centers.

Trial registration: ClinicalTrials.gov identifier, ChiCTR2400085276 (Version 2.0 June 04, 2024),  https://www.chictr.org.cn .

Trial sponsor: Shandong Second Medical university, Weifang, Shandong. Contact name: Dechun Qin, Address: Shandong Second Medical university, Weifang Shandong. Email: 13562666589@163.com.

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来源期刊
Trials
Trials 医学-医学:研究与实验
CiteScore
3.80
自引率
4.00%
发文量
966
审稿时长
6 months
期刊介绍: Trials is an open access, peer-reviewed, online journal that will encompass all aspects of the performance and findings of randomized controlled trials. Trials will experiment with, and then refine, innovative approaches to improving communication about trials. We are keen to move beyond publishing traditional trial results articles (although these will be included). We believe this represents an exciting opportunity to advance the science and reporting of trials. Prior to 2006, Trials was published as Current Controlled Trials in Cardiovascular Medicine (CCTCVM). All published CCTCVM articles are available via the Trials website and citations to CCTCVM article URLs will continue to be supported.
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