Clinical Trials Directory

Trials / Completed

CompletedNCT03737630

Inspiratory Muscle Training in Individuals With Cystic Fibrosis

Effects of Inspiratory Muscle Training in Individuals Who Have Cystic Fibrosis

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
10 (actual)
Sponsor
Universidade Federal do Rio Grande do Norte · Academic / Other
Sex
All
Age
14 Years – 25 Years
Healthy volunteers
Not accepted

Summary

Cystic fibrosis is a genetic disease that affects some organs of the human body. Among them, the lungs tend to be the most affected due to the accumulation of mucus in the airways, which in addition to avoiding the passage of air, favors pulmonary infections. With the evolution of the condition, secondary complications arise, such as postural changes, decreased respiratory muscle strength, decreased functional capacity and, consequently, quality of life. Therefore, respiratory muscle training may be an intervention that improves the respiratory condition of these individuals, allowing an improvement in the quality of life and may delay the evolution of respiratory symptoms. Thus, this study aims to investigate a home protocol of respiratory muscle training on respiratory muscle strength, lung function, quality of life, posture and functional capacity in adolescents and adults with cystic fibrosis. The researchers believe that the training can cause an improvement in the studied variables, and can be inserted in the usual treatment of these patients.

Conditions

Interventions

TypeNameDescription
DEVICEInspiratory muscle trainingThis group will initiate inspiratory muscle training with 40% of the MIP load and each week will have a load increase of 10% of the initial MIP up to 4 weeks of training

Timeline

Start date
2019-08-05
Primary completion
2019-10-18
Completion
2020-01-31
First posted
2018-11-09
Last updated
2020-04-16

Locations

1 site across 1 country: Brazil

Source: ClinicalTrials.gov record NCT03737630. Inclusion in this directory is not an endorsement.