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Improving Functional Capacity in Fontan Patients Through Inspiratory Muscle Training

Boston Children's Hospital logo

Boston Children's Hospital

Status

Completed

Conditions

Single Ventricle
Congenital Heart Disease

Treatments

Device: THRESHOLD(TM) INSPIRATORY MUSCLE TRAINER

Study type

Interventional

Funder types

Other

Identifiers

NCT01977222
P00006063

Details and patient eligibility

About

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.

Enrollment

12 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

12 participants in 1 patient group

THRESHOLD(TM) INSPIRATORY MUSCLE TRAINER
Experimental group
Treatment:
Device: THRESHOLD(TM) INSPIRATORY MUSCLE TRAINER

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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