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

Author:

Combret YannORCID,Prieur Guillaume,Boujibar FairuzORCID,Gravier Francis-EdouardORCID,Smondack PaulineORCID,Le Roux Pascal,Bonnevie Tristan,Medrinal Clément,Reychler Grégory

Publisher

Elsevier BV

Subject

Pulmonary and Respiratory Medicine

Reference6 articles.

1. Cardiopulmonary exercise testing provides additional prognostic information in cystic fibrosis;Hebestreit;Am J Respir Crit Care Med,2019

2. Exercise-induced hypoxemia and cardiac arrhythmia in cystic fibrosis;Ruf;J Cyst Fibros,2009

3. Exercise testing and exercise training within cystic fibrosis centres across Australia and New Zealand: what is considered important and what is current practice?;Sawyer;Intern Med J,2019

4. Measurement properties of the one-minute sit-to-stand test in children and adolescents with cystic fibrosis: A multicenter randomized cross-over trial;Combret;PLOS ONE,2021

5. The 1-min sit-to-stand test—A simple functional capacity test in cystic fibrosis?;Radtke;J Cyst Fibros,2016

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