Coronary Artery Disease
Conditions
Interventions
This is a prospective, longitudinal, randomized, quantitative clinical study involving 43 participants. The experimental group consisted of 22 patients undergoing coronary artery bypass grafting (CABG
Sponsors
Universidade Federal do Piauí Campus Universitário Ministro Petrônio Portella
Universidade Federal do Piauí Campus Universitário Ministro Petrônio Portella
Hospital Universitário da Universidade Federal do Piauí
Eligibility
Inclusion criteria
Inclusion criteria: Volunteers undergoing Myocardial Revascularization surgery; able to complete the Cardiac Rehabilitation program phase II; both genders; without obesity; preserved cognition
Exclusion criteria
Exclusion criteria: Volunteers with diseases that limit functionality or that interfere with the performance of respiratory muscle training; do not sign the Informed Consent Form; fail to participate in one of the research stages; attend less than eight weeks or 24 sessions in the cardiac rehabilitation program.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to increase heart rate variability, assessed through the analysis of variables in the time and frequency domain, using predicted values ??for sex and age as a reference, pre and post intervention.;It is expected to improve lung volumes and capacities, assessed through spirometry, using predicted values ??for sex and age as a reference, pre and post intervention. | — |
Secondary
| Measure | Time frame |
|---|---|
| An increase in inspiratory muscle strength is expected, assessed by manovacuometry, using predicted values ??for sex and age as a reference, pre and post intervention.;An improvement in functional capacity is expected, assessed using the 6-minute walk test, using predicted values ??for sex and age as a reference, pre and post intervention.;An improvement in quality of life is expected, assessed using the Medical Outcomes Study 36-Item Short-form of Health Survey (SF-36) questionnaire, using the scores proposed by the questionnaire as a reference, pre and post intervention. | — |
Countries
Brazil
Contacts
Public ContactLúcia Santos
Universidade Federal do Piauí Campus Universitário Ministro Petrônio Portella
Outcome results
None listed