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Effects of home‐based telerehabilitation‐assisted inspiratory muscle training in patients with idiopathic pulmonary fibrosis: A randomized controlled trial

Background and Objective There are few studies that have used inspiratory muscle training (IMT) as an intervention for patients with isolated idiopathic pulmonary fibrosis (IPF). This study aimed to investigate and interpret the effects of home‐based telerehabilitation‐assisted IMT in patients with...

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Bibliographic Details
Published in:Respirology (Carlton, Vic.) Vic.), 2024-12, Vol.29 (12), p.1077-1084
Main Authors: Aktan, Rıdvan, Tertemiz, Kemal Can, Yiğit, Salih, Özalevli, Sevgi, Ozgen Alpaydin, Aylin, Uçan, Eyüp Sabri
Format: Article
Language:English
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Summary:Background and Objective There are few studies that have used inspiratory muscle training (IMT) as an intervention for patients with isolated idiopathic pulmonary fibrosis (IPF). This study aimed to investigate and interpret the effects of home‐based telerehabilitation‐assisted IMT in patients with IPF. Methods Twenty‐eight participants with IPF took part in the study. Lung function tests, functional exercise capacity by 6‐min walk distance (6MWD), dyspnoea perception by modified medical research council dyspnoea scale (mMRC), and inspiratory muscle strength by maximal inspiratory pressure (MIP) were assessed. IMT was performed twice a day, 7 days/week, for 8 weeks. The intervention group (n = 14) performed IMT at 50% of their baseline MIP while the control group (n = 14) performed IMT without applied resistance. Loading intensity was progressed by keeping the load at 4–6 on a modified Borg scale for the highest tolerable perceived respiratory effort for each patient. Results Dyspnoea based on mMRC score (p 
ISSN:1323-7799
1440-1843
1440-1843
DOI:10.1111/resp.14810