سامانه مدیریت نشریات علمی دانشگاه علوم پزشکی مشهد

Eshkil, Saeedeh, Mousavi, Seyedeh Farnaz, Sayedi, Seyed Javad, Kianifar, Hamid Reza, Sohrabi, Mehdi, Bakhtiari, Elham, Mashoughi, Morteza, Khodashenas, Ezzat. (1402). The Effect of Spark Physical Program (Sports, Play and Active Recreation for Kids) on Quality of Life and Spirometry in 6-18-Year-Old Children with Cystic Fibrosis. , 11(5), 17790-17799. doi: 10.22038/ijp.2023.71553.5236
Saeedeh Eshkil; Seyedeh Farnaz Mousavi; Seyed Javad Sayedi; Hamid Reza Kianifar; Mehdi Sohrabi; Elham Bakhtiari; Morteza Mashoughi; Ezzat Khodashenas. "The Effect of Spark Physical Program (Sports, Play and Active Recreation for Kids) on Quality of Life and Spirometry in 6-18-Year-Old Children with Cystic Fibrosis". , 11, 5, 1402, 17790-17799. doi: 10.22038/ijp.2023.71553.5236
Eshkil, Saeedeh, Mousavi, Seyedeh Farnaz, Sayedi, Seyed Javad, Kianifar, Hamid Reza, Sohrabi, Mehdi, Bakhtiari, Elham, Mashoughi, Morteza, Khodashenas, Ezzat. (1402). 'The Effect of Spark Physical Program (Sports, Play and Active Recreation for Kids) on Quality of Life and Spirometry in 6-18-Year-Old Children with Cystic Fibrosis', , 11(5), pp. 17790-17799. doi: 10.22038/ijp.2023.71553.5236
Eshkil, Saeedeh, Mousavi, Seyedeh Farnaz, Sayedi, Seyed Javad, Kianifar, Hamid Reza, Sohrabi, Mehdi, Bakhtiari, Elham, Mashoughi, Morteza, Khodashenas, Ezzat. The Effect of Spark Physical Program (Sports, Play and Active Recreation for Kids) on Quality of Life and Spirometry in 6-18-Year-Old Children with Cystic Fibrosis. , 1402; 11(5): 17790-17799. doi: 10.22038/ijp.2023.71553.5236

The Effect of Spark Physical Program (Sports, Play and Active Recreation for Kids) on Quality of Life and Spirometry in 6-18-Year-Old Children with Cystic Fibrosis

Journal of Pediatric Perspectives
مقاله 11، دوره 11، شماره 5، مرداد 2023، صفحه 17790-17799    اصل مقاله (221.57 K)
نوع مقاله: original article
شناسه دیجیتال (DOI): 10.22038/ijp.2023.71553.5236
نویسندگان
Saeedeh Eshkil1؛ Seyedeh Farnaz Mousavi2؛ Seyed Javad Sayedi3؛ Hamid Reza Kianifar4؛ Mehdi Sohrabi5؛ Elham Bakhtiari6؛ Morteza Mashoughi7؛ Ezzat Khodashenas* 8
1Neonatologist, department of pediatrics, Faculty of medicine Mashhad university of medical sciences, Mashhad, Iran
2Subspecialist Assistant of Neonatology, department of pediatrics, Faculty of medicine Mashhad university of medical sciences, Mashhad, Iran
3CF. Research center, Faculty of medicine Mashhad university of medical science. Mashhad Iran
4Allergy Research Center, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran
5professor of motor behavior in sport science faculty, Ferdowsi university of Mashhad, Mashhad, Iran
6Assistant professor, Clinical Research Development Unit, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran
7Neonatal research center , Mashhad university of medical sciences, Mashhad, Iran
8Neonatal Research Center, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
چکیده
Background: The effect of SPARK physical education program on lung function in cystic fibrosis patients is not yet determined. SPARK (Sports, play and active recreation for kids) includes moving skills, aerobic games, jogging or walking, aerobic dance and jump rope. Regarding the high prevalence of cystic fibrosis and its destructive effects on the lungs, the aim of this study was to evaluate the lung function and quality of life before and after undergoing the SPARK physical education program, in children with cystic fibrosis.
Method: In this quasi-experimental study, all patients with cystic fibrosis aged 6-18 years referred to the cystic fibrosis clinic of Dr. Sheikh Hospital in Mashhad, Iran, were enrolled. The patients attended the 12-week SPARK training program (3 sessions per week, each session 45 minutes). The quality of life questionnaire for patients with cystic fibrosis, including self-examination and parental tests, along with spirometry indices (FEV1, FVC, FEV1/FVC, FEF25-75) were filled out before and after intervention for all patients.
Results: The mean and standard deviation of patients' age were 9.85±2.67 years, and 65% of patients were female. The FEV1 was significantly different before and after the SPARK physical education program (P=0.03), and the respiratory component of quality of life significantly increased after intervention (P=0.002). The overall score of quality of life from parents’ point of view was 2.87 ± 0.38 which increased to 2.99 ± 0.38 after the intervention.
Conclusion: SPARK training program may improve the spirometric parameters in children with cystic fibrosis. It also had a significant effect on improving the patients’ quality of life, especially in the respiratory component.
کلیدواژه‌ها
Cystic fibrosis؛ Quality of life؛ SPARK motor program؛ Spirometry
مراجع
  1. Egan M. Cystic Fibrosis. In: Kliegman RM, Stanton BF, Schor, NF, et al (eds). Nelson Textbook of Pediatrics. 20th. Philadelphia: Saunders. 2016; Pp 2098- 2113.
  2. Cutting GR. Cystic fibrosis genetics: from molecular understanding to clinical application. Nature Reviews Genetics. 2015; 16(1):45-56.
  3. Dastgiri S, Pourbonyadi MJ, Mirzae T. Prevalence of abnormalities genetically in east Azarbaijan province. Urmia Med J 2010; 21:339-346.(Persian)
  4. Stoltz DA, Meyerholz DK, Welsh MJ. Origins of cystic fibrosis lung disease. New England Journal of Medicine. 2015; 372(4):351-62.
  5. Sly PD, Gangell CL, Chen L, Ware RS ,Ranganathan S, Mott LS, Murray CP, Stick SM; AREST CF Investigators. Risk factors for bronchiectasis in children with cystic fibrosis. New England Journal of Medicine. 2013; 3 68(21) :1963-70.
  6. Flume PA, Robinson KA, O'Sullivan BP, Finder JD, Vender RL, Willey-Courand D-B, White TB, Marshall BC; Clinical Practice Guidelines for Pulmonary Therapies Committee. Cystic fibrosis pulmonary guidelines: airway clearance therapies. Respiratory care. 2009; 54(4):522-37.
  7. Flass T, Narkewicz MR. Cirrhosis and other liver disease in cystic fibrosis. Journal of Cystic Fibrosis. 2013; 12(2):116-24.
  8. Debray D, Kelly D, Houwen R, Strandvik B, Colombo C. Best practice guidance for the diagnosis and management of cystic fibrosis-associated liver disease. Journal of Cystic Fibrosis. 2011; 10:S29-S36.
  9. Rueegg CS, Barben J, Hafen GM, Moeller A, Jurca M, Fingerhut R, Kuehni CE; Swiss Cystic Fibrosis Screening Group. Newborn screening for cystic fibrosis - the parent perspective. Journal of Cystic Fibrosis. 2015.
  10. Khalilzadeh S, Kahkouee S, Hassanzad M, Parsanejad N, Baghaie N, Boloursaz MR. The correlation of brody high resolution computed tomography scoring system with clinical status and pulmonary function test in patients with cystic fibrosis. Iranian Journal of Medical Sciences. 2011; 36:18-23.
  11. Cohen-Cymberknoh M, Shoseyov D, Kerem E. Managing cystic fibrosis: strategies that increase life expectancy and improve quality of life. American journal of respiratory and critical caremedicine. 2011; 183(11):1463-71.
  12. Schalock RL. Reconsidering the conceptualization and measurement of quality of life. Quality of life. 1996; 1(9):123-39.
  13. Mahmoudi G-R, Shariati A, Behnampour N. Relationship between quality of life and coping among hemodialysis patients in hospitals. Journal of Gorgan University of Medical Sciences. 2003; 5(2):43-52.
  14. Moradi H , Khodashenas E, Sohrabi M, Teymoori S, Shayan-Noshabadi A. The effect of Spark motor program on sensory-motor functions in children with developmental coordination disorder:KAUMS Journal (FEYZ) 19 (5), 391-398.
  15. Fadayi Ardestani M. The effect of selection on growth of basic motor skills, 10-7 years female educationally mentally retarded. [Thesis]. Tehran. Tehran University. 2003. [In Persian].
  16. Mollanorouzi K, Khalaji H, Shikh M, Akbari, H. Effect of selected movement skills program of manipulation for children 4 to 6 years. J Growth Motor learning–Sport 2010; 7: 5-21. [In Persian].
  17. Henry B, Aussage P, Grosskopf C, Goehrs J-M. Development of the Cystic Fibrosis Questionnaire (CFQ) for assessing quality of life in pediatric and adult patients. Quality of Life Research. 2003; 12(1):63-76.
  18. Dwyer TJ, Zainuldin R, Daviskas E, Bye PTP, Alison JA. Effects of treadmill exercise versus Flutter on respiratory flow and sputum properties in adults with cystic fibrosis: a randomised, controlled, cross-over trial. Dwyer et al. BMC Pulmonary Medicine (2017) 17:14.
  19. Quittner AL, Buu A, Messer MA, Modi AC, Watrous M. Development and validation of The Cystic Fibrosis Questionnaire in the United States: a health-related quality-of-life measure for cystic fibrosis. Chest Journal. 2005; 128(4):2347-54.
  20. Ariyafar Y. Face and Content validity of Persian Version of Disease-Specific Measure of Health-Related Quality of Life for Children with Cystic Fibrosis (CFQ) (Doctoral dissertation, Tabriz University of Medical Sciences, School of Rehabilitation.
  21. Dwyer TJ, Zainuldin R, Daviskas E, Bye PTP, Alison JA "Effects of treadmill exercise versus Flutter on respiratory flow and sputum properties in adults with cystic fibrosis: a randomized, controlled, cross-over trial." BMC pulmonary medicine 17.1 (2017): 1-8.‏
  22. Schmidt AM, Jacobsen U, Bregnballe V, Olesen HV, Ingemann-Hansen T, Thastum M, Oluf Schiøtz P. Exercise and quality of life in patients with cystic fibrosis: a 12-week intervention study. Physiotherapy theory and practice. 2011 Nov 1; 27(8):548-56.
  23. Thomas C, Mitchell P, O’Rourke P, Wainwright C. Quality-of-life in children and adolescents with cystic fibrosis managed in both regional outreach and cystic fibrosis center settings in Queensland. The Journal of pediatrics. 2006; 148(4):508-16. e1.
  24. Kianifar H-R, Bakhshoodeh B, Hebrani P, Behdani F. Qulaity of life in cystic fibrosis children. Iranian journal of pediatrics. 2013; 23(2):149.
  25. Quittner AL, Barker DH, Snell C, Grimley ME, Marciel K, Cruz I. Prevalence and impact of depression in cystic fibrosis. Current opinion in pulmonary medicine. 2008; 14(6):582-8.
  26. Havermans T, Colpaert K, Dupont LJ. Quality of life in patients with Cystic Fibrosis: association with anxiety and depression. Journal of Cystic Fibrosis. 2008; 7(6):581-4.
  27. Szyndler JE, Towns SJ, van Asperen PP, McKay KO. Psychological and family functioning and quality of life in adolescents with cystic fibrosis. Journal of Cystic Fibrosis. 2005; 4(2):135-44.
  28. Schmitz T, Henrich G, Goldbeck L. [Quality of life with cystic fibrosis--aspects of age and gender]. Klinische Padiatrie. 2005; 218(1):7-12.
  29. Goldbeck L, Zerrer S, Schmitz TG. Monitoring quality of life in outpatients with cystic fibrosis: feasibility and longitudinal results. Journal of Cystic Fibrosis. 2007; 6(3):171-8.
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