Improving Functional Capacity in Fontan Patients Through Inspiratory Muscle Training
Primary Purpose
Congenital Heart Disease, Single Ventricle
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
THRESHOLD(TM) INSPIRATORY MUSCLE TRAINER
Sponsored by
About this trial
This is an interventional treatment trial for Congenital Heart Disease
Eligibility Criteria
Inclusion Criteria:
- 18 years of age and older
- Fontan physiology
- Undergoing cardiopulmonary stress testing
- Able to complete a previous cardiopulmonary stress test in the preceding 24 months
- Ability to comply with the inspiratory muscle training protocol
- Ability to return for repeat stress testing and pulmonary function testing 12 weeks after enrollment
- Ability to provide informed consent
Exclusion Criteria:
- Status post cardiac transplantation
- Current pregnancy or plans to become pregnant within the next 3 months (for females of childbearing potential)
- Active respiratory infection
- Active cigarette smoker
- Baseline oxygen saturation <90% at the previous clinic visit or exercise test
- Forced expired volume in 1 s and/or vital capacity <60% of predicted at the previous exercise test
- Cardiac surgery or catheter-based procedure in the preceding 18 months or planned surgery or catheter-based procedure within the next 3 months
Sites / Locations
- Children's Hospital, Boston
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
THRESHOLD(TM) INSPIRATORY MUSCLE TRAINER
Arm Description
Outcomes
Primary Outcome Measures
Change in Peak VO2 Between Baseline and Post-inspiratory Muscle Training Measurements.
Secondary Outcome Measures
Change in Innocor Measurement (Inert Gas Rebreathing Method) of Cardiac Output at Peak Exercise
Change in SF-36 Health Survey Score (Physical Component Summary)
The 36-Item Short Form (SF-36) Health Survey is a disease-generic survey of an individual's perceived health status and health-related quality of life. There are eight scaled scores, which are the weighted sums of the questions in their section. Each scale is transformed into a 0-100 scale on the assumption that each question carries equal weight. The lower the score the more disability. The higher the score the less disability. These eight scales are then used to calculate (using a proprietary formula) two summary scores: the physical component score (PCS), representing the four physical health scales (physical functioning, role physical, bodily pain, general health), and the mental component score (MCS), representing the four mental health scales (mental health, role emotional, vitality, social functioning). Component scores are norm-based with a mean of 50 (standardized to the US population) and a standard deviation of 10.
Full Information
NCT ID
NCT01977222
First Posted
October 25, 2013
Last Updated
October 14, 2017
Sponsor
Boston Children's Hospital
1. Study Identification
Unique Protocol Identification Number
NCT01977222
Brief Title
Improving Functional Capacity in Fontan Patients Through Inspiratory Muscle Training
Official Title
Improving Functional Capacity in Fontan Patients Through Inspiratory Muscle Training
Study Type
Interventional
2. Study Status
Record Verification Date
October 2017
Overall Recruitment Status
Completed
Study Start Date
December 2013 (undefined)
Primary Completion Date
March 2015 (Actual)
Study Completion Date
March 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Boston Children's Hospital
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Mechanisms that typically result in increased cardiac output, such as inotropic support, increased heart rate, and decreased afterload, have a blunted effect in Fontan circulation. The "thoracic pump" is a contributor to venous return that has been largely unexplored in patients with Fontan physiology. Inspiratory muscle training can improve the performance of competitive athletes across a range of sports and can improve quality of life and functional capacity in heart failure patients, presumably by reducing inspiratory muscle fatigue and possibly by improving peripheral blood flow during exercise. One could surmise that the effects of these changes would be particularly important in the Fontan population. The investigators propose to study the effects of inspiratory muscle training on exercise and pulmonary function parameters in a cohort of adult Fontan patients.
The investigators hypothesize that a 12-week program of inspiratory muscle training with an inspiratory impedance threshold device will improve inspiratory muscle strength and endurance, and that this will translate into improved exercise performance in patients with Fontan physiology.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Congenital Heart Disease, Single Ventricle
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
12 (Actual)
8. Arms, Groups, and Interventions
Arm Title
THRESHOLD(TM) INSPIRATORY MUSCLE TRAINER
Arm Type
Experimental
Intervention Type
Device
Intervention Name(s)
THRESHOLD(TM) INSPIRATORY MUSCLE TRAINER
Intervention Description
Subjects will be provided with noseclips and a threshold impedance device set to 40% of their measured maximal inspiratory pressure and will be trained on using the device. Specifically, subjects will be instructed to breathe through the inspiratory muscle training device while wearing noseclips at a rate of 12 to 16 breaths per minute for 30 minutes a day, 5 days a week for 12 consecutive weeks. Each subject will be provided a customized schedule for increasing resistance by 2 cm H2O every 2 weeks to a maximum resistance of 41 cm H2O.
Primary Outcome Measure Information:
Title
Change in Peak VO2 Between Baseline and Post-inspiratory Muscle Training Measurements.
Time Frame
Baseline and after 12 weeks of training
Secondary Outcome Measure Information:
Title
Change in Innocor Measurement (Inert Gas Rebreathing Method) of Cardiac Output at Peak Exercise
Time Frame
12 weeks
Title
Change in SF-36 Health Survey Score (Physical Component Summary)
Description
The 36-Item Short Form (SF-36) Health Survey is a disease-generic survey of an individual's perceived health status and health-related quality of life. There are eight scaled scores, which are the weighted sums of the questions in their section. Each scale is transformed into a 0-100 scale on the assumption that each question carries equal weight. The lower the score the more disability. The higher the score the less disability. These eight scales are then used to calculate (using a proprietary formula) two summary scores: the physical component score (PCS), representing the four physical health scales (physical functioning, role physical, bodily pain, general health), and the mental component score (MCS), representing the four mental health scales (mental health, role emotional, vitality, social functioning). Component scores are norm-based with a mean of 50 (standardized to the US population) and a standard deviation of 10.
Time Frame
12 weeks
Other Pre-specified Outcome Measures:
Title
Change in Maximum Voluntary Ventilation
Time Frame
12 weeks
Title
Change in Maximal Inspiratory Pressure
Time Frame
Baseline and after 12 weeks of training
Title
Change in Oxygen Pulse at Peak Exercise
Time Frame
12 weeks
Title
Change in Peak Work Rate During Exercise
Time Frame
Baseline and after 12 weeks of training
Title
Change in VE/VCO2 Slope (Ratio) During Exercise
Time Frame
Baseline and after 12 weeks of training
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
18 years of age and older
Fontan physiology
Undergoing cardiopulmonary stress testing
Able to complete a previous cardiopulmonary stress test in the preceding 24 months
Ability to comply with the inspiratory muscle training protocol
Ability to return for repeat stress testing and pulmonary function testing 12 weeks after enrollment
Ability to provide informed consent
Exclusion Criteria:
Status post cardiac transplantation
Current pregnancy or plans to become pregnant within the next 3 months (for females of childbearing potential)
Active respiratory infection
Active cigarette smoker
Baseline oxygen saturation <90% at the previous clinic visit or exercise test
Forced expired volume in 1 s and/or vital capacity <60% of predicted at the previous exercise test
Cardiac surgery or catheter-based procedure in the preceding 18 months or planned surgery or catheter-based procedure within the next 3 months
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Fred Wu, MD
Organizational Affiliation
Boston Children's Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Children's Hospital, Boston
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States
12. IPD Sharing Statement
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Improving Functional Capacity in Fontan Patients Through Inspiratory Muscle Training
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