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High Intensity interval Training after Cardiac Resynchronization Therapy.

High Intensity interval Training after Cardiac Resynchronization Therapy.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON22642
Enrollment
50
Registered
2010-09-25
Start date
2010-10-01
Completion date
Unknown
Last updated
2024-06-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Heart Failure Cardiac Resynchronization Therapy High Intensity Training

Interventions

Exercise training is performed 3 times as week during 12 weeks. Patients perform the training program at the department of physical therapy of their own hospital. The HIT program is adapted from the s
in this way, patients with ischemia or ventricular arrhythmias during high-intensity exercise can be excluded. Third, CRT devices with implantable defibrillator (ICD) will be programmed in a way that

Sponsors

None
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Written informed consent; 2. Systolic heart failure due to ischemic cardiomyopathy (due to one or more myocardial infarction, as confirmed with echocardiography) or dilating cardiomyopathy (no history of myocardial infarction, no proven ischemia, no congenital heart disease en no severe valve disorder); 3. Left ventricular ejection fraction (LVEF) < 35% before CRT; 4. New York Heart Association (NYHA) class III before CRT.

Exclusion criteria

Exclusion criteria: 1. Myocardial infarction or unstable angina less than 3 months prior to inclusion; 2. Clinical signs of decompensated heart failure; 3. Ventricular tachycardia or ischemia during exercise; 4. Participation in a training program (&#8805;2/week) in the last year; 5. Intracardiac shunts or congenital heart disease limiting exercise capacity; 6. Orthopaedic, vascular, pulmonary, neuromuscular and other disease limiting exercise capacity.

Design outcomes

Primary

MeasureTime frame
Changes in peak VO&#8322; after 3 months of HIT in CHF patients that underwent CRT as compared to a control group that received no training.

Secondary

MeasureTime frame
Training-induced changes in: 1. Left ventricular function assessed by left ventricular ejection fraction and end systolic volume; 2. Submaximal exercise capacity assessed by the rate of recovery of oxygen uptake after submaximal exercise (time constant of recovery, tau-rec); 3. Quality of life assessed by the Minnesota living with heart failure Questionnaire; 4. Plasma NT-pro BNP, a prognostic biomarker of heart failure.

Contacts

Public ContactR.F. Spee

De Run 4600

r.spee@mmc.nl+31 (0)40 8888200

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)