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Perceptions towards physical activity in adult lung transplant recipients with cystic fibrosis
Author(s) -
Martina Wietlisbach,
Christian Benden,
Angela Koutsokera,
Kathleen Jahn,
Paola M. Soccal,
Thomas Radtke
Publication year - 2020
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0229296
Subject(s) - cystic fibrosis , medicine , quality of life (healthcare) , lung transplantation , physical therapy , perception , lung , gerontology , psychology , nursing , neuroscience
Background Barriers and motives towards physical activity (PA) in lung transplant (LTx) recipients with cystic fibrosis (CF) are largely unknown. We aimed to explore perceptions towards PA in LTx recipients with CF to better understand individuals’ needs and preferences. Methods Participants completed an online survey at two Swiss LTx and one follow-up shared care centre between June and December 2018. Results One hundred and eleven individuals completed the survey (87.4% response rate). Overall, survey participants perceive PA as important for their daily life and health. Perceived motives of PA were improving muscle strength , endurance and quality of life (QoL), to feel better , fun , to achieve personal goals and having more energy for everyday life . Fatigue was the most common perceived barrier to PA and associated with poorer QoL (r = -0.43, p <0.001) and health status (r = -0.31, p = 0.001). Participants with lung allograft dysfunction (LAD, n = 20) reported lower habitual PA ( p = 0.009) and health status ( p = 0.011), and rated shortness of breath , bad weather and concerns regarding lung rejection higher than those without LAD (all p <0.05). When we asked how an optimal training programme should look like, the majority would prefer individual, non-supervised (60%), outdoor (77%), endurance training (90%), once or twice a week (47%) for 40–60 minutes (48%). Only a minority of patients (14%) would be willing to use exercise applications for their home-based training. Conclusions LTx recipients with CF value PA as important for their health. People with CF should be encouraged individually by their multidisciplinary transplant team to implement PA in their daily life, potential barriers should be identified and addressed. Overall, knowledge on perceived barriers and motives for PA should be considered in the development of future patient-centred PA programmes.

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