Ignite Creation Date:
2024-05-06 @ 8:47 AM
Last Modification Date:
2024-10-26 @ 12:05 PM
Study NCT ID:
NCT02823587
Status:
UNKNOWN
Last Update Posted:
2017-08-21
First Post:
2016-05-19
Brief Title:
Pulmonary Rehabilitation in Non-Cystic Fibrosis Bronchiectasis
Sponsor:
University of Sao Paulo
Organization:
University of Sao Paulo
Study Overview
Official Title:
Effects of Pulmonary Rehabilitation on Secretion Transport Inflammation and Respiratory System Strength and Quality of Life in Patients With Bronchiectasis
Status:
UNKNOWN
Status Verified Date:
2016-12
Last Known Status:
RECRUITING
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The purpose of this study is to assess the effect of pulmonary rehabilitation on the transport of secretions inflammation and respiratory resistance and its repercussions on the quality of life in patients with bronchiectasis
Detailed Description:
Bronchiectasis is characterized by pathological and irreversible dilation of bronchi caused by the inefficient removal of secretions and microorganisms and the perpetuation of inflammatory processes induced by chronic or recurrent infections causing more damage to the airways that result in infections and greater lesion airways and lung parenchyma Pulmonary rehabilitation in people with bronchiectasis aims to improve exercise capacity through effects on aerobic capacity and peripheral muscles and to improve disease control and quality of life The aim this study is to evaluate the effects of pulmonary rehabilitation on the transport of secretions inflammation and respiratory resistance and its repercussions on the quality of life in patients with bronchiectasis In this study 60 volunteers of both sexes aged between 18-60 years adequate the inclusion criteria which will be assessed by lung function tests the saccharin transport time the inflammatory markers in the airways the respiratory system resistance and quality of life scales Volunteers will be randomly divided in pulmonary rehabilitation PRG and control groups CG that will be subdivided in bronchiectasis and healthy subgroups In the PRG group they will receive supervised physical training twice a week and will be instructed to adopt a routine of home exercises while CG will be informed about the benefits of physical activities All volunteers will be evaluated after 8 weeks of the baseline and at the end of the research Data evolution will be collected from medical records and notes of the medical team and physical therapy that will follow the routine of these participants
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None