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MOVE-CRT: A study to describe physical activity in heart failure patients with cardiac resynchronization therapy (CRT)

Conditions
Heart failure
10019280
Registration Number
NL-OMON53635
Lead Sponsor
niversitair Medisch Centrum Utrecht
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Not specified
Target Recruitment
30
Inclusion Criteria

- Diagnosis of chronic heart failure according to the prevailing guidelines
- Elective first-time implantation of CRT (pacemaker (CRT-P) or defibrillator
(CRT-D)) in UMCU
- Adult (age >= 18 years)

Exclusion Criteria

- Scheduled cardiac surgery within 3 months
- Problems to fill in questionnaires
- Problems to wear an activity monitor
- Previously implanted pacemaker or defibrillator device
- On an active waiting list for left ventricular assist device (LVAD)
implantation or heart transplantation
- Inability to provide informed consent

Study & Design

Study Type
Observational non invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>• Daily physical activity<br /><br>• Self-reported activity level </p><br>
Secondary Outcome Measures
NameTimeMethod
<p>• Submaximal Exercise Capacity<br /><br>• Exercise Motivation<br /><br>• Health related Quality of life and well-being.<br /><br>• Anxiety and depression<br /><br>• LV volumes and function measured by echocardiography<br /><br>• NT-proBNP levels<br /><br>• Number of missing questionnaires at T0, T1, T2 and T3</p><br>
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