Abstract

Introduction: Idiopathic pulmonary fibrosis (IPF) is a chronic, devastating, interstitial lung disease, with few therapeutic options. IPF is characterized by pulmonary restriction, dyspnea, hypoxemia, exercise intolerance and poor quality of life (QOL). Aims and objective: We aimed to examine the effect of exercise training (ET) on clinical outcomes and on quality of life and symptoms in IPF patients. Methods: Subjects who met current criteria for IPF were randomized to a 3-month pulmonary rehabilitation program (n _ 14) or to a control group (n _ 10). The rehabilitation group participated in twiceweekly, 90-min exercise sessions (24 total sessions). The control group maintained its preceding normal physical activity. 6-min walking distance (6MWD) test, 30-second chair-stand test, pulmonary function tests, dyspnea and QOL were assessed at baseline and at the end of the 12-week intervention. The SGRQ-I and a 5-point self-assessment of health were completed at baseline, after 3 months of intervention or observation. Results: Subjects in the rehabilitation group maintained significantly higher levels of physical activity throughout the 3-month rehabilitation program. SGRQ-I symptom domain scores improved considerably by _9 _ 22 in the rehabilitation group, whereas in the control group they worsened Significant differences were observed between the ET and the control groups in raw mean: Δ6MWD, 94 m, p Conclusion: ET improves exercise tolerance, functional capacity, pulmonary function, dyspnea and QOL in patients with IPF and should be considered the standard care for IPF.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call