The Impact of Physical Activity on Clinical Outcomes in Children with Cystic Fibrosis: A Narrative Review

Background: Cystic fibrosis (CF) is a chronic genetic disease marked by progressive lung function decline and increased respiratory infections. Emerging evidence supports the role of physical exercise in improving lung function, aerobic capacity, and quality of life in pediatric CF patients. Methods...

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Published inChildren (Basel) Vol. 12; no. 7; p. 831
Main Authors Rosolia Capasso, Chiara, Miniato, Antonio Luca, Di Filippo, Paola, Di Ludovico, Armando, Di Pillo, Sabrina, Chiarelli, Francesco, Sferrazza Papa, Giuseppe Francesco, Attanasi, Marina
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 23.06.2025
MDPI
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ISSN2227-9067
2227-9067
DOI10.3390/children12070831

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Abstract Background: Cystic fibrosis (CF) is a chronic genetic disease marked by progressive lung function decline and increased respiratory infections. Emerging evidence supports the role of physical exercise in improving lung function, aerobic capacity, and quality of life in pediatric CF patients. Methods: We reviewed randomized clinical trials and observational studies from the last ten years, sourced from PubMed and Google Scholar. Included studies involved children and adolescents (0–18 years) with CF and assessed physical exercise as a primary intervention to improve lung function, aerobic fitness, quality of life, or hospitalization rates. Results: Aerobic training, particularly when combined with strength training, improves cardiorespiratory fitness and muscle strength without compromising nutritional status. High-Intensity Interval Training and Inspiratory Muscle Training show potential but need further validation. Supervised, personalized exercise programs are key to promoting adherence and optimizing outcomes. Conclusions: Exercise-based interventions in pediatric CF should evolve toward personalized, technology-enhanced, and sustainable models. Integrating wearable devices, adapting programs to individual needs, and leveraging early parental involvement may enhance engagement and outcomes, especially in the era of CFTR modulator therapies.
AbstractList Cystic fibrosis (CF) is a chronic genetic disease marked by progressive lung function decline and increased respiratory infections. Emerging evidence supports the role of physical exercise in improving lung function, aerobic capacity, and quality of life in pediatric CF patients.BACKGROUNDCystic fibrosis (CF) is a chronic genetic disease marked by progressive lung function decline and increased respiratory infections. Emerging evidence supports the role of physical exercise in improving lung function, aerobic capacity, and quality of life in pediatric CF patients.We reviewed randomized clinical trials and observational studies from the last ten years, sourced from PubMed and Google Scholar. Included studies involved children and adolescents (0-18 years) with CF and assessed physical exercise as a primary intervention to improve lung function, aerobic fitness, quality of life, or hospitalization rates.METHODSWe reviewed randomized clinical trials and observational studies from the last ten years, sourced from PubMed and Google Scholar. Included studies involved children and adolescents (0-18 years) with CF and assessed physical exercise as a primary intervention to improve lung function, aerobic fitness, quality of life, or hospitalization rates.Aerobic training, particularly when combined with strength training, improves cardiorespiratory fitness and muscle strength without compromising nutritional status. High-Intensity Interval Training and Inspiratory Muscle Training show potential but need further validation. Supervised, personalized exercise programs are key to promoting adherence and optimizing outcomes.RESULTSAerobic training, particularly when combined with strength training, improves cardiorespiratory fitness and muscle strength without compromising nutritional status. High-Intensity Interval Training and Inspiratory Muscle Training show potential but need further validation. Supervised, personalized exercise programs are key to promoting adherence and optimizing outcomes.Exercise-based interventions in pediatric CF should evolve toward personalized, technology-enhanced, and sustainable models. Integrating wearable devices, adapting programs to individual needs, and leveraging early parental involvement may enhance engagement and outcomes, especially in the era of CFTR modulator therapies.CONCLUSIONSExercise-based interventions in pediatric CF should evolve toward personalized, technology-enhanced, and sustainable models. Integrating wearable devices, adapting programs to individual needs, and leveraging early parental involvement may enhance engagement and outcomes, especially in the era of CFTR modulator therapies.
Background: Cystic fibrosis (CF) is a chronic genetic disease marked by progressive lung function decline and increased respiratory infections. Emerging evidence supports the role of physical exercise in improving lung function, aerobic capacity, and quality of life in pediatric CF patients. Methods: We reviewed randomized clinical trials and observational studies from the last ten years, sourced from PubMed and Google Scholar. Included studies involved children and adolescents (0–18 years) with CF and assessed physical exercise as a primary intervention to improve lung function, aerobic fitness, quality of life, or hospitalization rates. Results: Aerobic training, particularly when combined with strength training, improves cardiorespiratory fitness and muscle strength without compromising nutritional status. High-Intensity Interval Training and Inspiratory Muscle Training show potential but need further validation. Supervised, personalized exercise programs are key to promoting adherence and optimizing outcomes. Conclusions: Exercise-based interventions in pediatric CF should evolve toward personalized, technology-enhanced, and sustainable models. Integrating wearable devices, adapting programs to individual needs, and leveraging early parental involvement may enhance engagement and outcomes, especially in the era of CFTR modulator therapies.
Cystic fibrosis (CF) is a chronic genetic disease marked by progressive lung function decline and increased respiratory infections. Emerging evidence supports the role of physical exercise in improving lung function, aerobic capacity, and quality of life in pediatric CF patients. We reviewed randomized clinical trials and observational studies from the last ten years, sourced from PubMed and Google Scholar. Included studies involved children and adolescents (0-18 years) with CF and assessed physical exercise as a primary intervention to improve lung function, aerobic fitness, quality of life, or hospitalization rates. Aerobic training, particularly when combined with strength training, improves cardiorespiratory fitness and muscle strength without compromising nutritional status. High-Intensity Interval Training and Inspiratory Muscle Training show potential but need further validation. Supervised, personalized exercise programs are key to promoting adherence and optimizing outcomes. Exercise-based interventions in pediatric CF should evolve toward personalized, technology-enhanced, and sustainable models. Integrating wearable devices, adapting programs to individual needs, and leveraging early parental involvement may enhance engagement and outcomes, especially in the era of CFTR modulator therapies.
Audience Academic
Author Di Ludovico, Armando
Rosolia Capasso, Chiara
Di Filippo, Paola
Sferrazza Papa, Giuseppe Francesco
Attanasi, Marina
Chiarelli, Francesco
Miniato, Antonio Luca
Di Pillo, Sabrina
AuthorAffiliation 1 Pediatric Allergy and Pulmonology Unit, Department of Pediatrics, University of Chieti-Pescara, Via dei Vestini n°5, 66100 Chieti, Italy; chiara.rosoliacapasso@studenti.unich.it (C.R.C.); antonioluca.miniato@studenti.unich.it (A.L.M.); paola.difilippo@asl2abruzzo.it (P.D.F.); armando.diludovico@studenti.unich.it (A.D.L.); sabrina.dipillo@asl2abruzzo.it (S.D.P.); chiarelli@unich.it (F.C.)
2 Department of Neurorehabilitation Sciences, Casa di Cura Igea, 20144 Milan, Italy; g.sferrazza@casacuraigea.it
AuthorAffiliation_xml – name: 2 Department of Neurorehabilitation Sciences, Casa di Cura Igea, 20144 Milan, Italy; g.sferrazza@casacuraigea.it
– name: 1 Pediatric Allergy and Pulmonology Unit, Department of Pediatrics, University of Chieti-Pescara, Via dei Vestini n°5, 66100 Chieti, Italy; chiara.rosoliacapasso@studenti.unich.it (C.R.C.); antonioluca.miniato@studenti.unich.it (A.L.M.); paola.difilippo@asl2abruzzo.it (P.D.F.); armando.diludovico@studenti.unich.it (A.D.L.); sabrina.dipillo@asl2abruzzo.it (S.D.P.); chiarelli@unich.it (F.C.)
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adolescents
physical fitness
pulmonary function
aerobic fitness
exercise
training
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Snippet Background: Cystic fibrosis (CF) is a chronic genetic disease marked by progressive lung function decline and increased respiratory infections. Emerging...
Cystic fibrosis (CF) is a chronic genetic disease marked by progressive lung function decline and increased respiratory infections. Emerging evidence supports...
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SubjectTerms aerobic fitness
Aerobics
Children & youth
Clinical outcomes
Clinical trials
Cystic fibrosis
Exercise
Medical prognosis
Medical research
Medicine, Experimental
Muscle strength
Mutation
Parent and child
Parenting
Patient outcomes
Patients
Pediatrics
Physical fitness
Physical therapy
pulmonary function
Review
Sports training
Strength training
Teenagers
training
Weight training
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Title The Impact of Physical Activity on Clinical Outcomes in Children with Cystic Fibrosis: A Narrative Review
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