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 in | Children (Basel) Vol. 12; no. 7; p. 831 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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23.06.2025
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ISSN | 2227-9067 2227-9067 |
DOI | 10.3390/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. |
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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.) |
Author_xml | – sequence: 1 givenname: Chiara surname: Rosolia Capasso fullname: Rosolia Capasso, Chiara – sequence: 2 givenname: Antonio Luca surname: Miniato fullname: Miniato, Antonio Luca – sequence: 3 givenname: Paola surname: Di Filippo fullname: Di Filippo, Paola – sequence: 4 givenname: Armando surname: Di Ludovico fullname: Di Ludovico, Armando – sequence: 5 givenname: Sabrina surname: Di Pillo fullname: Di Pillo, Sabrina – sequence: 6 givenname: Francesco surname: Chiarelli fullname: Chiarelli, Francesco – sequence: 7 givenname: Giuseppe Francesco surname: Sferrazza Papa fullname: Sferrazza Papa, Giuseppe Francesco – sequence: 8 givenname: Marina orcidid: 0000-0001-6513-3160 surname: Attanasi fullname: Attanasi, Marina |
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Cites_doi | 10.1038/318384a0 10.1001/archpedi.1938.01980140114013 10.1016/j.jcf.2021.11.011 10.1186/1465-9921-14-32 10.1123/jpah.2017-0011 10.1378/chest.10-1508 10.1378/chest.10-1158 10.1002/ppul.25039 10.1056/NEJM199212173272504 10.2196/45896 10.3390/nu14050933 10.1515/jpem-2012-0012 10.3390/ijerph19137923 10.3390/children11020240 10.3390/healthcare10112205 10.7326/M13-0636 10.1159/000375170 10.1183/09031936.00062409 10.3390/ijns6010018 10.1183/09059180.00008112 10.1155/2010/670640 10.1186/1824-7288-38-2 10.1016/j.rmed.2019.01.013 10.3390/healthcare10122520 10.1183/09031936.00228013 |
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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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