Effects of Muscle Trainins Inspiratory Linked to Cardiac Rehabilitation Post-operative of CABG Surgery

NCT ID: NCT02742350

Last Updated: 2017-04-28

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 20 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2015-09-10
• Study Completion Date: 2016-12-30

Brief Summary

Heart surgery procedures are still widely used worldwide for the treatment of patients with heart problems, and rates of complications in the postoperative period related to them remain high. In these patients, physical conditioning programs result in improved functional capacity, and reducing the heart rate and systolic blood pressure. The inspiratory muscle training is also emerging as a valuable strategy in the treatment of cardiac patients. The study of the interaction between cardiac rehabilitation and high intensity IMT about these changes is not yet understood in this population. The aim of this study is to assess the effects of inspiratory muscle training high intensity associated with cardiac rehabilitation exercise performance of patients in the postoperative period of CABG surgery.

Detailed Description

It is a controlled, randomized clinical trial in which patients were randomly assigned randomly after referral to cardiac rehabilitation: Group 1 IMT-HI, group 2 - IMT-HI control. The evaluator of outcomes is blinded as to groups. The study protocol lasts 36 sessions for both groups. The group 1 patients performs cardiac rehabilitation protocol for 40 minutes with cardio and stretching and also inspiratory muscle training protocol of high intensity with 50% load increase in maximal inspiratory pressure during the first two weeks, 60% of MIP in third and fourth week, 70% of MIP in the fifth and sixth week and 80% MIP in the seventh and eighth week. The group 2 patients only perform the cardiac rehabilitation protocol for 40 minutes with aerobic exercise and stretching.

Conditions

Cardiovascular Diseases

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

IMT+Exercise

The inspiratory muscle training protocol (IMT) high intensity is achieved with a device with linear load pressure (POWERbreathe Plus Light Resistance®, SP, BR) that allows loads up to -90cmH2O. IMT is performed for 36 sessions (12 weeks) with weekly frequency of three times a week under supervision prior to the cardiac rehabilitation. The training protocol consists of five series with 10 repetitions each set until the 8th week with increase in the number of sets of repetitions of the 8th to 12th week, with two minutes or according to patient feedback using the modified Borg scale . Aerobic training lasts 40 minutes (5 minutes heating 30 minute workout and 5 minutes desaqueciemento. During training vital signs such as heart rate, blood pressure (BP) and peripheral oxygen saturation (SpO2) are evaluated and the feeling of effort the patient should not exceed the level of 8 according to the modified Borg scale.

Group Type: EXPERIMENTAL

IMT - POWERbreathe Plus Light Resistance®, SP, BR

Intervention Type: DEVICE

POWERbreathe Plus Light Resistance®, SP, BR

Exercise Control

Aerobic Exercise and Stretching

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

IMT - POWERbreathe Plus Light Resistance®, SP, BR

POWERbreathe Plus Light Resistance®, SP, BR

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

• Patients in the postoperative period of elective CABG
• Between the fourteenth and the thirtieth day after surgery
• Between 30 and 70 years old

Exclusion Criteria

• Decompensated heart failure
• Unstable angina
• Moderate respiratory disease severe
• Active infectious disease or fever
• Disabling peripheral vascular disease
• Unstable ventricular arrhythmias
• Use of cardiac pacemaker.

• Minimum Eligible Age: 30 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Federal University of Health Science of Porto Alegre

OTHER

Sponsor Role: lead

Responsible Party

Rodrigo Della Méa Plentz

Clinical Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Rodrigo Della Méa Plentz

Porto Alegre, Rio Grande do Sul, Brazil

Countries

Brazil

Other Identifiers

IMT+exercise-CABG

Identifier Type: -

Identifier Source: org_study_id