NCT07161219尚未招募不适用
Implementation of New Exercise Protocols in Cardiac Rehabilitation.
Cliniques universitaires Saint-Luc- Université Catholique de Louvain0 个研究点目标入组 80 人开始时间: 2025年12月1日最近更新:
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 80
- 主要终点
- Maximal inspiratory pressure
研究概览
简要总结
- Primary Objective: To evaluate the effects of complementary exercise protocols in cardiac rehabilitation (CR), such as inspiratory muscle training (IMT), by assessing inspiratory muscle strength.
- Secondary Objectives: To assess functional capacity, quality of life (QoL), and pulmonary function.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 80 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •- Patient meeting the conditions of the permanent life support agreement following hospitalization for a cardiac condition such as: acute myocardial infarction; coronary surgery; therapeutic percutaneous endovascular intervention on the coronary arteries, under medical imaging guidance; therapeutic percutaneous endovascular intervention on the heart, under medical imaging guidance; surgery for congenital or acquired heart malformation; surgery for valvular lesion; heart transplantation; resistant angina (to be specified by detailed history, medical history, and technical examinations, justifying multidisciplinary care); cardiomyopathy with left ventricular dysfunction (to be specified by detailed history, medical history, and technical examinations, justifying multidisciplinary care).
- •Patient aged between 18 and 80 years.
- •Patient capable of giving informed consent.
- •Patient registered for permanent life support at the CuSL.
- •Patient capable of understanding instructions in French. - Patient with prior medical consent and clinically stable.
排除标准
- •- Minor (<18 years old).
- •Pregnant woman.
- •Patient unable to provide informed consent.
- •Patient with cognitive, neurological, or orthopedic limitations.
- •Patient with mobility or musculoskeletal difficulties incompatible with physical activity.
- •Clinical instability.
研究组 & 干预措施
control group
No Intervention
intervention group
Experimental
干预措施: inspiratory muscle training (Device)
结局指标
主要结局
Maximal inspiratory pressure
时间窗: 1 year
次要结局
未报告次要终点
研究者
Dayez Martin
Principal investigator
Cliniques universitaires Saint-Luc- Université Catholique de Louvain
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