Expired Study
This study is not currently recruiting Study Participants on ClinicalConnection.com. If you would like to find active studies please search for clinical trials.

Boston, Massachusetts 02115


Purpose:

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.


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


NCT ID:

NCT01977222


Primary Contact:

Principal Investigator
Fred Wu, MD
Boston Children’s Hospital


Backup Contact:

N/A


Location Contact:

Boston, Massachusetts 02115
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: November 20, 2017

Modifications to this listing: Only selected fields are shown, please use the link below to view all information about this clinical trial.


Click to view Full Listing

This study is not currently recruiting Study Participants on ClinicalConnection.com. The form below is not enabled.