Effect of Physical Activity Program on the Quality of Life of Children with Cystic Fibrosis at School Age: A

Ashrafalsadat Hakim1, Seyedeh Kowsar Tabatabaei2, Seyed Mohammad Reza Mirkarimi3

  • 1Nursing Care Research Center in Chronic Diseases, Department of Nursing, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.

Tanaffos
|October 19, 2022
PubMed

Insights

A physical activity program (PAP) significantly improved the quality of life for children with cystic fibrosis (CF). This intervention demonstrated feasibility and effectiveness in enhancing physical, emotional, social, and academic aspects for children with CF.

Area of Science:

  • Pediatrics
  • Public Health
  • Exercise Science

Background:

  • Cystic fibrosis (CF) is a serious inherited disorder with significant mortality.
  • Children with CF often experience reduced quality of life due to the disease's impact.

Purpose of the Study:

  • To evaluate the impact of a physical activity program (PAP) on the quality of life in school-aged children with CF.
  • To determine the feasibility and effectiveness of PAP as an intervention for pediatric CF patients.

Main Methods:

  • A randomized controlled trial involving 70 children with CF, divided into intervention and control groups.
  • Data collected using demographic questionnaires and the Pediatric Quality of Life Inventory.
  • Statistical analysis included Chi-square, independent t-tests, and paired t-tests (p<0.05).

Main Results:

  • No significant demographic or baseline quality of life differences between groups.
  • The intervention group showed significant improvements in physical, emotional, social, and academic quality of life post-PAP (P<0.001).
  • The control group exhibited no significant changes in quality of life before and after the study period.

Conclusions:

  • Physical activity programs are effective in enhancing the quality of life for children with cystic fibrosis.
  • PAP is a feasible and beneficial intervention for improving the overall well-being of pediatric CF patients.
Abstract