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临床试验/jRCT1030230680
jRCT1030230680招募中不适用

Effects of Outpatient Cardiac Rehabilitation and Home Exercise Therapy in Patients with Heart Failure: TRANSITION-HF (TRANSITION-HF )

Gunma University Hospital0 个研究点目标入组 50 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
招募中
入组人数
50
主要终点
-

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Single Arm Study
干预模型
Single Assignment
主要目的
Treatment Purpose
盲法
Open(masking Not Used)

入排标准

年龄范围
18age old over 至 No limit(—)

入选标准

  • Patients aged 18 years and over
  • Patients with compensated heart failure
  • (i) stable weight without increased diuretics for more than 1 week
  • (ii) no symptoms of congestion (no orthopnea, edema, ascites, jugular vein rage)
  • (iii) no anginal symptoms, no arrhythmias of clinical concern
  • (iv) systolic blood pressure more than or equal to 80 mmHg and no orthostatic hypotension
  • Patients scheduled for induction of outpatient cardiac rehabilitation
  • Patients with basic ADLs
  • Patients with written informed consent

排除标准

  • Pulmonary arterial hypertension, significant left heart valvular disease (severe regurgitation or moderate or greater stenosis), cardiomyopathy, acute coronary syndrome, complex adult congenital heart disease
  • Patients with severe orthopaedic disease that makes it difficult to implement a cardiac rehabilitation programme.
  • Patients with dementia, which makes it difficult to implement cardiac rehabilitation programmes.
  • Patients with contraindications to resistance training (1) NYHA classification IV, (2) left ventricular outflow tract stenosis, (3) non-compensated heart failure, (4) uncontrolled arrhythmia (increasing trend of supraventricular and ventricular arrhythmias), (5) severe and symptomatic aortic stenosis, (6) uncontrolled diabetes mellitus, and (7) uncontrolled uncontrolled hypertension (>180/110 mmHg), (8) severe pulmonary hypertension (mean pulmonary arterial pressure >55 mmHg), (9) complicated by acute aortic dissection (thrombosed), (10) severe heart failure (terminal ))
  • (5) Patients with an implanted pacemaker or defibrillator with heart rate limitation.
  • (6) Patients deemed unsuitable as research subjects by the principal investigators and subinvestigators.

结局指标

主要结局

-

six-minute walk distance

次要结局

未报告次要终点

研究者

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