Cardiovascular, Pulmonary and Skeletal Muscle Evaluation Postoperative in Fontan Patients: Effects of Exercise Training
Primary Purpose
Congenital Heart Disease, Single Ventricle, Univentricular Heart
Status
Completed
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
Aerobic Exercise Training
Inspiratory Muscle Training
No Exercise Training
Sponsored by
About this trial
This is an interventional treatment trial for Congenital Heart Disease focused on measuring Fontan, Exercise, Pulmonary Function, Aerobic Capacity, Skeletal Muscle, Neurovascular control, Functional capacity
Eligibility Criteria
Inclusion Criteria:
- Both gender, aged between 12 and 30 years
- Patients undergoing the Fontan operation with time postoperatively ≥5 years
- Clinically stable patients, no arrhythmia in the last electrocardiogram or clinical assessment
- Consent by the cardiologist
- Patients who voluntarily signed the consent form.
Exclusion Criteria:
- Patients with hypoplastic left heart syndrome
- Changes that reduce musculoskeletal walking skills
- Neurological sequelae, patients with associated genetic syndrome, disturbance cognitive or psychiatric
- Patients with a history of ventricular arrhythmias, cardio respiratory arrest, users of anti-arrhythmic drugs and / or underwent implantation of pacemaker
- Atrial arrhythmia requiring treatment in the last 6 months
- Patients with heart failure not controlled by medications and lung hypertension
- Patients with protein-losing enteropathy
- Severe hypoxemia (oxygen saturation <80% at rest)
- Symptomatic patients with a diagnosis of diaphragmatic paresis or paralysis postoperative patients, with or without plication
- Patients with moderate to severe asthma
- Patients who live outside the area of Sao Paulo
Sites / Locations
- InCor Heart Institute
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Active Comparator
Active Comparator
Arm Label
Aerobic Exercise Training Group
Inspiratory Muscle Training Group
No Exercise Trainint Group
Arm Description
Aerobic Training: Aerobic training and muscle strength exercise for upper and lower limbs, 3 times a week for 4 months.
Respiratory Training: muscle training using POWERbreathe device, 7 times a week, 3 series of 30 repetitions per day, for 4 months.
No Physical Activity: Control group (usual care)
Outcomes
Primary Outcome Measures
Improvement exercise tolerance and physical capacity
Change in parameters by cardiopulmonary exercise test; increase in lung volumes and capacities; improvement by neurovascular control and skeletical muscle metabolism
Secondary Outcome Measures
Full Information
NCT ID
NCT02283255
First Posted
September 3, 2014
Last Updated
December 3, 2022
Sponsor
University of Sao Paulo
Collaborators
Fundação de Amparo à Pesquisa do Estado de São Paulo
1. Study Identification
Unique Protocol Identification Number
NCT02283255
Brief Title
Cardiovascular, Pulmonary and Skeletal Muscle Evaluation Postoperative in Fontan Patients: Effects of Exercise Training
Official Title
Cardiovascular, Pulmonary and Skeletal Muscle Evaluation in Patients With Univentricular Physiology in the Late Postoperative Period of the Fontan Surgery: Effects of Exercise Training
Study Type
Interventional
2. Study Status
Record Verification Date
December 2022
Overall Recruitment Status
Completed
Study Start Date
January 31, 2013 (Actual)
Primary Completion Date
January 30, 2016 (Actual)
Study Completion Date
October 30, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Sao Paulo
Collaborators
Fundação de Amparo à Pesquisa do Estado de São Paulo
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Introduction: The Fontan operation is the surgical treatment in most patients with either anatomic or functional single ventricles. In this operation, the subpulmonary ventricle is bypassed, connecting the systemic veins directly to the pulmonary arteries. The lack of a subpulmonary ventricle is associated with a nonpulsatile pulmonary flow and triggers a sequence of adaptive mechanisms along the life of these patients. The most frequent consequence of these adaptative mechanisms is the reduction in functional capacity, objectively measured by the decrease in peak oxygen consumption (VO2). So, cardiovascular and pulmonary functioning and skeletal muscle alterations can explain exercise intolerance in these patients.
Objectives: 1. To compare the cardiovascular, pulmonary, and musculoskeletal system variables in clinically stable Fontan patients with Healthy subjects; 2. To correlate the variables of the cardiovascular, pulmonary, and skeletal muscle with the functional capacity in Fontan patients; 3. To identify predictors of low functional capacity in this population; 4. To evaluate four-month aerobic exercise and inspiratory muscle training on functional capacity, pulmonary function, and autonomic control in patients after Fontan operation and compare to the group with no exercise training.
Methods: All subjects were submitted to cardiovascular, pulmonary, and skeletal muscle evaluation at baseline to perform a cross-sectional study comparing Fontan Patients (FP) with Healthy Controls (HC). In addition, the FP accepted to participate in the longitudinal clinical trial to evaluate exercise programs were randomized into three groups: Aerobic Exercise Training (AET), Inspiratory Muscle Training (IMT), and Non-exercise Training Group (NET, a control group). All patient groups (AET, IMT, NET) were reassessed after four months of training or under usual care.
Expected Outcomes: This study expects to demonstrate that impaired pulmonary function, altered neurovascular control, and reduced skeletal muscle could be an additional potential mechanism for reducing functional capacity in clinically stable Fontan patients. And this impairment could be diminished by exercise training, enhancing physical capacity, and exercise tolerance.
Detailed Description
All subjects were submitted to cardiovascular magnetic resonance, echocardiography, cardiopulmonary exercise test, complete lung function, catecholamine and B-type natriuretic peptide (BNP) plasmatic levels, microneurography, venous occlusion plethysmography, six-minute walk test, phosphorus magnetic resonance spectroscopy (31P MRS) and magnetic resonance imaging (MRI) of skeletal muscle and quality of life (QoL) using the Short Form Health Survey (SF36) in the baseline. Comparative analyzes of the different systems of the two groups were done as well as tests to identify the predictors of low functional capacity in Fontan groups (FG).
The evaluation was done at baseline in healthy subjects. And in the Fontan group at baseline and after four months of exercise training or usual care.
AET Protocol: Four-month supervised exercise training was performed in the hospital three times a week, 60-min exercise sessions (48 sessions in total). Each session consisted of 40min on a treadmill, 15 min of personal light resistance training (including chest press, squat, pull down, leg extension, shoulder press, calf raises, leg curl, and sit-ups), and 5min of cool down and stretching. The AET was individually prescribed according to their heart rate (HR) from maximal cardiopulmonary exercise testing (CPT), and patients exercised between the ventilatory threshold (VT) and respiratory compensation point (RCP). HR, systolic blood pressure, oxygen saturation, and exhaustion (i.e., Borg scale from 7 to 20) were monitored during the sessions. An exercise physiologist supervised all sessions. In the first 12 weeks, HR was maintained at T frequency. Between the 12th to 24thweek, there was a progressive increase in the effort, and HR was supported between AT and RCP. In the last 12 sessions of the program, HR was maintained close to RCP frequency.
IMT Protocol: Four months of exercise training were carried out daily, three sets of 30 repetitions using the POWERbreathe® device (POWERbreathe International Limited, Southam, UK), three sets of 30 repetitions. Maximal inspiratory pressure (MIP) measures were performed in all patients before the intervention, and patients exercised at 60% of individual MIP. Patients were instructed to inhale using diaphragm musculature, trying to expand the rib cage to avoid the use of accessory muscles, and breathing at a rate of 12 to 16 breaths/min. A nose clip was worn to ensure patients breathed exclusively through the training device. All patients had a supervised session of IMT with a physiotherapist once a week for the first two months and once every two weeks for the last two months. The load was adjusted during the supervised sessions. Patients were encouraged to maintain their habitual activities during the protocol.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Congenital Heart Disease, Single Ventricle, Univentricular Heart
Keywords
Fontan, Exercise, Pulmonary Function, Aerobic Capacity, Skeletal Muscle, Neurovascular control, Functional capacity
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
60 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Aerobic Exercise Training Group
Arm Type
Active Comparator
Arm Description
Aerobic Training: Aerobic training and muscle strength exercise for upper and lower limbs, 3 times a week for 4 months.
Arm Title
Inspiratory Muscle Training Group
Arm Type
Active Comparator
Arm Description
Respiratory Training: muscle training using POWERbreathe device, 7 times a week, 3 series of 30 repetitions per day, for 4 months.
Arm Title
No Exercise Trainint Group
Arm Type
Active Comparator
Arm Description
No Physical Activity: Control group (usual care)
Intervention Type
Other
Intervention Name(s)
Aerobic Exercise Training
Other Intervention Name(s)
AET
Intervention Description
Supervised aerobic and light muscle resistance exercise training
Intervention Type
Other
Intervention Name(s)
Inspiratory Muscle Training
Other Intervention Name(s)
IMT
Intervention Description
Inspiratory muscle training with POWERbreathe device
Intervention Type
Other
Intervention Name(s)
No Exercise Training
Other Intervention Name(s)
NET
Intervention Description
Usual care
Primary Outcome Measure Information:
Title
Improvement exercise tolerance and physical capacity
Description
Change in parameters by cardiopulmonary exercise test; increase in lung volumes and capacities; improvement by neurovascular control and skeletical muscle metabolism
Time Frame
Baseline and 4 months
Other Pre-specified Outcome Measures:
Title
Improvement in the functional capacity post exercise training program
Description
Increase at least 20% cardiopulmonary exercise test parameters: VO2 peak, oxygen pulse and VE/VCO2 slope
Time Frame
baseline and 4 months
Title
Improvement in pulmonary function post physical exercise program
Description
Achieve at least 80% of predicted values for age at pulmonary function testing: spirometry, plethysmography, carbon monoxide diffusion capacity and maximal inspiratory pressure
Time Frame
baseline and 4 months
Title
Change in autonomic function post exercise training program
Description
Decrease bursts/min and bursts per 100 heart beats by at least 20% from baseline by directly measured by microneurography : direct muscle sympathetic nerve activity (MSNA)
Time Frame
baseline and 4 months
Title
Improvement in peripheral blood flow post exercise training program
Description
Increase forearm blood flow in mL/min/100mL
Time Frame
baseline and 4 months
Title
Change in the plasma epinephrine level post exercise training program
Description
Decrease of plasma epinephrine level from baseline
Time Frame
baseline and 4 months
Title
Change in muscle metabolism post exercise training program
Description
Increase of the amplitudes of the phosphocreatine, inorganic phosphate and ATP from baseline by 31P-MRS: Quadriceps femoral 31P-MRS
Time Frame
baseline and 4 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
12 Years
Maximum Age & Unit of Time
30 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Both gender, aged between 12 and 30 years
Patients undergoing the Fontan operation with time postoperatively ≥5 years
Clinically stable patients, no arrhythmia in the last electrocardiogram or clinical assessment
Consent by the cardiologist
Patients who voluntarily signed the consent form.
Exclusion Criteria:
Patients with hypoplastic left heart syndrome
Changes that reduce musculoskeletal walking skills
Neurological sequelae, patients with associated genetic syndrome, disturbance cognitive or psychiatric
Patients with a history of ventricular arrhythmias, cardio respiratory arrest, users of anti-arrhythmic drugs and / or underwent implantation of pacemaker
Atrial arrhythmia requiring treatment in the last 6 months
Patients with heart failure not controlled by medications and lung hypertension
Patients with protein-losing enteropathy
Severe hypoxemia (oxygen saturation <80% at rest)
Symptomatic patients with a diagnosis of diaphragmatic paresis or paralysis postoperative patients, with or without plication
Patients with moderate to severe asthma
Patients who live outside the area of Sao Paulo
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marcelo B Jatene, MD,PhD
Organizational Affiliation
Heart Institute, University of Sao Paulo, Medical School
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Aida LR Turquetto, PhD student
Organizational Affiliation
Heart Institute, University of Sao Paulo, Medical School
Official's Role
Principal Investigator
Facility Information:
Facility Name
InCor Heart Institute
City
Sao Paulo
ZIP/Postal Code
05403000
Country
Brazil
12. IPD Sharing Statement
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Cardiovascular, Pulmonary and Skeletal Muscle Evaluation Postoperative in Fontan Patients: Effects of Exercise Training
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