Validity and reliability of the one-minute sit-to-stand test for the measurement of cardio-respiratory responses in children with cystic fibrosis.

Combret, Yann;Prieur, Guillaume;Boujibar, Fairuz;Gravier, Francis-Edouard;Reychler, Gregory;et.al.
(2022) Pulmonology — Vol. 28, n° 2, p. 137-139 (2022)

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Authors
  • Combret, YannUCLouvain
    Author
  • Prieur, GuillaumeUCLouvain
    Author
  • Boujibar, Fairuz
    Author
  • Gravier, Francis-Edouard
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Abstract
(en) TO THE EDITOR : Maintaining exercise tolerance in individuals with cystic fibrosis (CF) is essential to limit the impact of the disease and increase survival. The cardio-respiratory responses to exercise provide an indication of exercise tolerance, which can be used to prevent unwanted effects during exercise. The 6-minute walk test (6MWT) is the gold standard field test for the evaluation of exercise capacity, however this test requires space and cannot always be performed. [...]
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Citations

Combret, Y., Prieur, G., Boujibar, F., Gravier, F.-E., Smondack, P., Le Roux, P., Bonnevie, T., Medrinal, C., & Reychler, G. (2022). Validity and reliability of the one-minute sit-to-stand test for the measurement of cardio-respiratory responses in children with cystic fibrosis. Pulmonology, 28(2), 137-139. https://doi.org/10.1016/j.pulmoe.2021.10.005 (Original work published 2022)