pacemaker
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Will be included in the study sedentary patients with artificial pacemaker for at least six months, of both sexes, without cognitive deficit, aged 18 years or more, in a follow-up regimen in the Laboratory of Electrophysiology and Pacemaker of the HC-UFG or at the Arrhythmias and Pacemaker Ambulatory of Santa Casa de Misericórdia de Goiânia.
Exclusion criteria
Exclusion criteria: Patients who practice regular physical activity (> 150 minutes of moderate intensity physical activity per week), unstable angina, implantable cardioverter defibrillator (ICD), cardiac resynchronizer, cardiac surgery less than three months, heart failure ( NYHA class III-IV), diabetes mellitus (fasting glycemia> 180 mg / dL and / or glycated hemoglobin> 7.0%), chronic renal failure (glomerular filtration <50 ml / min / 1.73m2), left ventricular thrombi, any clinical condition that would prevent the practice of physical activity or exercise test (ET), and the impossibility of attending the rehabilitation sector three times a week during the intervention period.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 10% increase in exercise group VO2max after 12 weeks of a cardiac rehabilitation program, determined through the exercise test.;Increased scores on the domains of the SF-36 and AQUAREL (Assessment of quality of life related events) quality of life questionnaires of the exercise group after 12 weeks of a cardiac rehabilitation program. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes are not expected | — |
Countries
Brazil
Contacts
Universidade Federal de Goiás