NL-OMON41024已完成不适用
Randomized clinical trial for an extended cardiac rehabilitation program using telemonitoring - TeleCaRe study
niversitair Medisch Centrum Sint Radboud0 个研究点目标入组 120 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 120
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •- Patients participating in cardiac rehabilitation (minimal attendance of 80% in physical program)
- •- Signed written informed consent
- •- One of the following criteria:
- •o Patients with an acute coronary syndrome, including myocardial infarction (MI) within 3 months
- •prior to start cardiac rehabilitation program
- •o Patients that underwent a percutaneous coronary intervention (PCI) within 3 months prior to
- •prior to start cardiac rehabilitation program
- •o Patients that received coronary artery bypass grafting (CABG) within 3 months prior to start
- •cardiac rehabilitation program
排除标准
- •- Contraindication to cardiac rehabilitation
- •- Mental impairment leading to inability to cooperate
- •- Severe impaired ability to exercise
- •- Signs of cardiac ischemia and/or a positive exercise testing on cardiac ischemia
- •- Insufficient knowledge of the Dutch language
- •- No access, availability or insufficient knowledge of a computer with internet
- •- Implanted cardiac device (pacemaker, ICD)
研究者
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