Self-Reported Physical Activity and Exercise Patterns in Children With Sickle Cell Disease

Osarhiemen A Omwanghe1, Devin S Muntz1, Soyang Kwon1

  • 11 Ann & Robert H. Lurie Children's Hospital of Chicago.

Insights

Children with sickle cell disease (SCD) engage in moderate-to-vigorous physical activity (PA) for shorter durations. Disease impact and physical functioning challenges create barriers to PA participation for these children.

Area of Science:

  • Pediatric Health
  • Hematology
  • Exercise Science

Background:

  • Sickle cell disease (SCD) is a genetic blood disorder impacting physical functioning.
  • Understanding physical activity (PA) patterns is crucial for managing SCD in children.
  • Previous research has not fully explored PA in children with SCD compared to national samples.

Purpose of the Study:

  • To compare physical activity (PA) patterns in children with SCD to a national sample.
  • To identify factors associated with PA levels in children with SCD.
  • To examine participation in physical education and organized sports among children with SCD.

Main Methods:

  • A survey was administered to 100 children with SCD.
  • The survey included questions from the National Health and Nutrition Examination Survey (NHANES) Physical Activity Questionnaire.
  • Additional questions assessed disease impact, physical functioning, and participation in physical education and sports.

Main Results:

  • Children with SCD reported more days of moderate-to-vigorous intensity PA (MVPA) weekly but for shorter durations.
  • Fewer children with SCD met recommended daily durations for vigorous PA (VPA) and MVPA compared to NHANES participants.
  • Disease impact and physical functioning were negatively associated with PA participation.

Conclusions:

  • Children with SCD are active but for shorter durations at moderate-to-vigorous intensities.
  • Barriers to PA in SCD include negative beliefs about disease impact and impaired physical functioning.
  • Interventions should address these barriers to promote PA in children with SCD.
Abstract