评估儿童心脏移植受者与远程医疗视频游戏相关的高强度间歇训练运动计划

Christopher M. Spence MD , Rae Foshaug , Samira Rowland BSc , Amanda Krysler MSc , Jennifer Conway MD, MSc , Simon Urschel MD , Lori West MD, PhD , Michael Stickland PhD , Pierre Boulanger MSc, PhD , John C. Spence PhD , Michael Khoury MD
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引用次数: 2

摘要

儿童心脏移植受者(HTRs)的运动能力、体力活动(PA)、健康相关的生活质量(HRQoL)和对PA的自我效能降低。运动干预已证明成人心脏移植受试者的运动能力和功能状态有所改善,对高强度间歇训练(HIIT)的作用产生了特别的兴趣。迄今为止,对儿科HTRs运动干预的研究是有限的,并且是非随机的。HIIT尚未在儿科HTRs中进行评估。因此,我们试图评估一项为期12周的随机交叉试验的安全性和可行性,该试验以家庭为基础,使用具有远程医疗和远程生理监测功能的循环测力计(MedBIKE)对儿科HTR进行视频游戏相关的HIIT干预。次要目标是评估干预对(1)运动能力、(2)PA、(3)HRQoL和对PA的自我效能的影响,以及(4)干预后6个月和12个月次要结果的持续变化。在对次要结果进行基线评估后,参与者将被随机分配接受MedBIKE干预(12周,36次疗程)或常规护理。在干预和重复评估之后,所有参与者都将交叉。随访评估将在MedBIKE干预后6个月和12个月进行。我们预计,MedBIKE干预将是可行的,并安全地在儿科HTRs中持续改善运动能力、PA、HRQoL和对PA的自我效能。这项研究将成为一项更大规模、多中心随机交叉试验的基础,并将有助于为儿科HTRs的运动康复计划提供信息。
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Evaluating a Telemedicine Video Game–Linked High-Intensity Interval Training Exercise Programme in Paediatric Heart Transplant Recipients

Paediatric heart transplant recipients (HTRs) have reduced exercise capacity, physical activity (PA), health-related quality of life (HRQoL), and self-efficacy towards PA. Exercise interventions have demonstrated improvements in exercise capacity and functional status in adult HTRs, with a specific emerging interest in the role of high-intensity interval training (HIIT). Studies of exercise interventions in paediatric HTRs have been limited and nonrandomized to date. HIIT has not yet been evaluated in paediatric HTRs. We thus seek to evaluate the safety and feasibility of a randomized crossover trial of a 12-week, home-based, video game–linked HIIT intervention using a cycle ergometer with telemedicine and remote physiological monitoring capabilities (MedBIKE) in paediatric HTRs. The secondary objective is to evaluate the impact of the intervention on (1) exercise capacity, (2) PA, (3) HRQoL and self-efficacy towards PA, and (4) sustained changes in secondary outcomes at 6 and 12 months after intervention. After a baseline assessment of the secondary outcomes, participants will be randomized to receive the MedBIKE intervention (12 weeks, 36 sessions) or usual care. After the intervention and a repeated assessment, all participants will cross over. Follow-up assessments will be administered at 6 and 12 months after the MedBIKE intervention. We anticipate that the MedBIKE intervention will be feasible and safely yield sustained improvements in exercise capacity, PA, HRQoL, and self-efficacy towards PA in paediatric HTRs. This study will serve as the foundation for a larger, multicentre randomized crossover trial and will help inform exercise rehabilitation programmes for paediatric HTRs.

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