Oonagh M Giggins, Julie Doyle, Suzanne Smith, Grainne Vavasour, Orla Moran, Shane Gavin, Nisanth Sojan, Gordon Boyle
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This pilot trial sought to test the ECME-CR platform and examine the efficacy and feasibility of a remote CR exercise program compared to a traditional center-based program.</p><p><strong>Methods: </strong>In all, 21 participants with CHD were recruited and assigned to either the intervention or control group. Both groups performed the same 8-week exercise program. Participants in the intervention group took part in web-based exercise classes and used the ECME-CR platform during the intervention period, whereas participants in the control group attended in-person classes. Outcomes were assessed at baseline and following the 8-week intervention period. The primary outcome measure was exercise capacity, assessed using a 6-minute walk test (6MWT). Secondary outcomes included measurement of grip strength, self-reported quality of life, heart rate, blood pressure, and body composition. A series of mixed between-within subjects ANOVA were conducted to examine the mean differences in study outcomes between and within groups. Participant adherence to the exercise program was also analyzed.</p><p><strong>Results: </strong>In all, 8 participants (male: n=5; age: mean 69.7, SD 7.2 years; height: mean 163.9, SD 5.4 cm; weight: mean 81.6, SD 14.1 kg) in the intervention group and 9 participants (male: n=9; age: mean 69.8, SD 8.2 years; height: mean 173.8, SD 5.2 cm; weight: mean 94.4, SD 18.0 kg) in the control group completed the exercise program. Although improvements in 6MWT distance were observed from baseline to follow-up in both the intervention (mean 490.1, SD 80.2 m to mean 504.5, SD 93.7 m) and control (mean 510.2, SD 48.3 m to mean 520.6, SD 49.4 m) group, no significant interaction effect (F<sub>1,14</sub>=.026; P=.87) nor effect for time (F<sub>1,14</sub>=2.51; P=.14) were observed. No significant effects emerged for any of the other secondary end points (all P>.0275). Adherence to the exercise program was high in both the intervention (14.25/16, 89.1%) and control (14.33/16, 89.6%) group. No adverse events or safety issues were reported in either group during the study.</p><p><strong>Conclusions: </strong>This pilot trial did not show evidence of significant positive effect for either the remotely delivered or center-based program. The 6MWT may not have been sufficiently sensitive to identify a change in this cohort of participants with stable CHD. This trial does provide evidence that remote CR exercise, supported with digital self-monitoring, is feasible and may be considered for individuals less likely to participate in traditional center-based programs.</p><p><strong>International registered report identifier (irrid): </strong>RR2-10.2196/31855.</p>","PeriodicalId":14706,"journal":{"name":"JMIR Cardio","volume":"7 ","pages":"e40283"},"PeriodicalIF":0.0000,"publicationDate":"2023-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9960022/pdf/","citationCount":"2","resultStr":"{\"title\":\"Remotely Delivered Cardiac Rehabilitation Exercise for Coronary Heart Disease: Nonrandomized Feasibility Study.\",\"authors\":\"Oonagh M Giggins, Julie Doyle, Suzanne Smith, Grainne Vavasour, Orla Moran, Shane Gavin, Nisanth Sojan, Gordon Boyle\",\"doi\":\"10.2196/40283\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Exercise-based cardiac rehabilitation (CR) is recommended for coronary heart disease (CHD). 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Outcomes were assessed at baseline and following the 8-week intervention period. The primary outcome measure was exercise capacity, assessed using a 6-minute walk test (6MWT). Secondary outcomes included measurement of grip strength, self-reported quality of life, heart rate, blood pressure, and body composition. A series of mixed between-within subjects ANOVA were conducted to examine the mean differences in study outcomes between and within groups. Participant adherence to the exercise program was also analyzed.</p><p><strong>Results: </strong>In all, 8 participants (male: n=5; age: mean 69.7, SD 7.2 years; height: mean 163.9, SD 5.4 cm; weight: mean 81.6, SD 14.1 kg) in the intervention group and 9 participants (male: n=9; age: mean 69.8, SD 8.2 years; height: mean 173.8, SD 5.2 cm; weight: mean 94.4, SD 18.0 kg) in the control group completed the exercise program. Although improvements in 6MWT distance were observed from baseline to follow-up in both the intervention (mean 490.1, SD 80.2 m to mean 504.5, SD 93.7 m) and control (mean 510.2, SD 48.3 m to mean 520.6, SD 49.4 m) group, no significant interaction effect (F<sub>1,14</sub>=.026; P=.87) nor effect for time (F<sub>1,14</sub>=2.51; P=.14) were observed. No significant effects emerged for any of the other secondary end points (all P>.0275). Adherence to the exercise program was high in both the intervention (14.25/16, 89.1%) and control (14.33/16, 89.6%) group. No adverse events or safety issues were reported in either group during the study.</p><p><strong>Conclusions: </strong>This pilot trial did not show evidence of significant positive effect for either the remotely delivered or center-based program. The 6MWT may not have been sufficiently sensitive to identify a change in this cohort of participants with stable CHD. 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引用次数: 2
摘要
背景:以运动为基础的心脏康复(CR)被推荐用于治疗冠心病(CHD)。然而,在全球范围内,对CR运动计划的不良吸收和不良依从性都有报道。远程提供CR运动课程可以消除传统医院或中心CR相关的一些障碍。目的:我们开发了一个定制平台,东部走廊医学工程中心心脏康复(ECME-CR),以支持远程提供CR运动。该试点试验旨在测试ECME-CR平台,并与传统的基于中心的计划相比,检查远程CR锻炼计划的有效性和可行性。方法:总共招募了21名冠心病患者,并将其分为干预组和对照组。两组都进行了相同的8周锻炼计划。干预组参与者在干预期间参加基于网络的运动课程并使用ECME-CR平台,而对照组参与者则参加面对面的课程。在基线和8周干预期后评估结果。主要结局指标是运动能力,通过6分钟步行测试(6MWT)进行评估。次要结果包括握力、自我报告的生活质量、心率、血压和身体成分的测量。进行了一系列混合的受试者间方差分析,以检查组间和组内研究结果的平均差异。参与者对锻炼计划的坚持程度也进行了分析。结果:共有8名参与者(男性:n=5;年龄:平均69.7岁,SD 7.2岁;身高:平均163.9,标准差5.4 cm;体重:平均81.6,SD 14.1 kg)干预组和9名参与者(男性:n=9;年龄:平均69.8岁,标准差8.2岁;身高:平均173.8,标准差5.2 cm;体重:平均94.4,标准差18.0 kg),对照组完成运动方案。虽然干预组(平均490.1 m, SD 80.2 m至平均504.5 m, SD 93.7 m)和对照组(平均510.2 m, SD 48.3 m至平均520.6 m, SD 49.4 m)从基线到随访均观察到6MWT距离的改善,但没有显著的相互作用效应(F1,14= 0.026;P= 0.87)与时间无关(F1,14=2.51;P=.14)。其他次要终点均无显著影响(P均> 0.0275)。干预组(14.25/16,89.1%)和对照组(14.33/16,89.6%)对运动计划的坚持度都很高。在研究期间,两组均未报告不良事件或安全问题。结论:该试点试验没有显示出远程交付或中心项目显著的积极影响的证据。6MWT可能不够敏感,无法识别这组稳定型冠心病患者的变化。这项试验确实提供了证据,证明在数字自我监控的支持下,远程CR锻炼是可行的,可以考虑为不太可能参与传统中心项目的个人提供支持。国际注册报告标识符(irrid): RR2-10.2196/31855。
Background: Exercise-based cardiac rehabilitation (CR) is recommended for coronary heart disease (CHD). However, poor uptake of and poor adherence to CR exercise programs have been reported globally. Delivering CR exercise classes remotely may remove some of the barriers associated with traditional hospital- or center-based CR.
Objective: We have developed a bespoke platform, Eastern Corridor Medical Engineering Centre-Cardiac Rehabilitation (ECME-CR), to support remotely delivered CR exercise. This pilot trial sought to test the ECME-CR platform and examine the efficacy and feasibility of a remote CR exercise program compared to a traditional center-based program.
Methods: In all, 21 participants with CHD were recruited and assigned to either the intervention or control group. Both groups performed the same 8-week exercise program. Participants in the intervention group took part in web-based exercise classes and used the ECME-CR platform during the intervention period, whereas participants in the control group attended in-person classes. Outcomes were assessed at baseline and following the 8-week intervention period. The primary outcome measure was exercise capacity, assessed using a 6-minute walk test (6MWT). Secondary outcomes included measurement of grip strength, self-reported quality of life, heart rate, blood pressure, and body composition. A series of mixed between-within subjects ANOVA were conducted to examine the mean differences in study outcomes between and within groups. Participant adherence to the exercise program was also analyzed.
Results: In all, 8 participants (male: n=5; age: mean 69.7, SD 7.2 years; height: mean 163.9, SD 5.4 cm; weight: mean 81.6, SD 14.1 kg) in the intervention group and 9 participants (male: n=9; age: mean 69.8, SD 8.2 years; height: mean 173.8, SD 5.2 cm; weight: mean 94.4, SD 18.0 kg) in the control group completed the exercise program. Although improvements in 6MWT distance were observed from baseline to follow-up in both the intervention (mean 490.1, SD 80.2 m to mean 504.5, SD 93.7 m) and control (mean 510.2, SD 48.3 m to mean 520.6, SD 49.4 m) group, no significant interaction effect (F1,14=.026; P=.87) nor effect for time (F1,14=2.51; P=.14) were observed. No significant effects emerged for any of the other secondary end points (all P>.0275). Adherence to the exercise program was high in both the intervention (14.25/16, 89.1%) and control (14.33/16, 89.6%) group. No adverse events or safety issues were reported in either group during the study.
Conclusions: This pilot trial did not show evidence of significant positive effect for either the remotely delivered or center-based program. The 6MWT may not have been sufficiently sensitive to identify a change in this cohort of participants with stable CHD. This trial does provide evidence that remote CR exercise, supported with digital self-monitoring, is feasible and may be considered for individuals less likely to participate in traditional center-based programs.
International registered report identifier (irrid): RR2-10.2196/31855.