Physical Activity and Quality of Life among Patients with Cystic Fibrosis

Bibliographic Data

ID15714900
AuthorsStavros Giannakoulakos (Aristotle University of Thessaloniki), Maria Gioulvanidou (Aristotle University of Thessaloniki), Evangelia Kouidi (0000-0002-5023-2542, Aristotle University of Thessaloniki), Pauline Peftoulidou (Aristotle University of Thessaloniki), S Kyrvasili (0000-0003-1268-9960, Aristotle University of Thessaloniki), Syrmo Styliani Kyrvasili (Pediatric Respiratory Unit, 3rd Paediatric Clinic, Aristotle University of Thessaloniki, Hippokration General Hospital of Thessaloniki, 54642 Thessaloniki, Greece), Parthena Savvidou (Aristotle University of Thessaloniki), Asterios Deligiannis (0000-0001-7765-1897, Aristotle University of Thessaloniki), John Tsanakas (Aristotle University of Thessaloniki), Elpis Hatziagorou (0000-0001-9505-2054, Aristotle University of Thessaloniki, corresponding author)
Year2022
Volume9
Issue11
Pages1665-1665
Publication date2022-10-31
Open AccessYes
TypeARTICLE
VenueChildren (JOURNAL)
Journal identifiersISSN: 2227-9067 • E-ISSN: 2227-9067
PublisherMultidisciplinary Digital Publishing Institute (PUBLISHER • CH)
DOI10.3390/children9111665
PMID36360393
OpenAlexW4308128844
LanguageEN
References cited46

The children with CF showed satisfactory PA levels, which positively correlated to their QoL. More research is needed on the effect of increased levels of habitual physical activity to establish the decline in pulmonary function among pwCF

Asthma · Correlation · Cystic fibrosis · Disease · Health related quality of life · Lung · Lung function · Physical activity · Physical therapy · Population · Pulmonary function testing · Quality of life (healthcare · Spirometry · Child Nutrition and Feeding Issues · Cystic Fibrosis Research Advances · Medicine · Pediatric health and respiratory diseases · Internal Medicine

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Open DOIOpen Access