Literature DB >> 28112012

Physical Activity in Boys With Duchenne Muscular Dystrophy Is Lower and Less Demanding Compared to Healthy Boys.

Lotte Heutinck1, Nadine van Kampen1, Merel Jansen1, Imelda J M de Groot1.   

Abstract

This study describes the amount of physical activity and perception of physical activity in boys with Duchenne muscular dystrophy (DMD) compared to healthy boys. A questionnaire described 6 domains of physical activity. Four Duchenne muscular dystrophy subgroups were made: early and late ambulatory, nonambulatory with relative good, or limited arm function. Eighty-four boys with Duchenne muscular dystrophy (15.0 ± 6.4 years) and 198 healthy boys (14.0 ± 4.3 years) participated. Daily activities were more passive for boys with Duchenne muscular dystrophy. Physical activity was less and low demanding compared to healthy boys. It decreased with disease severity ( P < .05), whereas screen time increased ( P < .05). Benefits of physical activity in boys with Duchenne muscular dystrophy were having fun and making friends. Barriers were lack of sport facilities and insufficient health. This study helps to quantify poor engagement in physical activity by boys with Duchenne muscular dystrophy, and demonstrates factors that contribute to it. Suggestions to stimulate physical activity are made.

Entities:  

Keywords:  Duchenne muscular dystrophy; neuromuscular disorders; perception of physical activity; physical activity; physical activity questionnaire

Mesh:

Year:  2017        PMID: 28112012     DOI: 10.1177/0883073816685506

Source DB:  PubMed          Journal:  J Child Neurol        ISSN: 0883-0738            Impact factor:   1.987


  6 in total

1.  Step Activity Monitoring in Boys with Duchenne Muscular Dystrophy and its Correlation with Magnetic Resonance Measures and Functional Performance.

Authors:  Kavya S Nair; Donovan J Lott; Sean C Forbes; Alison M Barnard; Rebecca J Willcocks; Claudia R Senesac; Michael J Daniels; Ann T Harrington; Gihan I Tennekoon; Kirsten Zilke; Erika L Finanger; Richard S Finkel; William D Rooney; Glenn A Walter; Krista Vandenborne
Journal:  J Neuromuscul Dis       Date:  2022

2.  Interventions for promoting physical activity in people with neuromuscular disease.

Authors:  Katherine Jones; Fiona Hawke; Jane Newman; James Al Miller; Joshua Burns; Djordje G Jakovljevic; Grainne Gorman; Douglass M Turnbull; Gita Ramdharry
Journal:  Cochrane Database Syst Rev       Date:  2021-05-24

3.  Producing a preference-based quality of life measure for people with Duchenne muscular dystrophy: a mixed-methods study protocol.

Authors:  Philip A Powell; Jill Carlton; Donna Rowen; John E Brazier
Journal:  BMJ Open       Date:  2019-03-09       Impact factor: 2.692

Review 4.  Mental health problems among adolescents and young adults with childhood-onset physical disabilities: A scoping review.

Authors:  Shalini Lal; Stephanie Tremblay; Danielle Starcevic; Melina Mauger-Lavigne; Dana Anaby
Journal:  Front Rehabil Sci       Date:  2022-09-06

5.  Assessing Physical Activity Using Accelerometers in Youth with Duchenne Muscular Dystrophy.

Authors:  David Arteaga; Thomas Donnelly; Kimberly Crum; Larry Markham; Mary Killian; W Bryan Burnette; Jonathan Soslow; Maciej S Buchowski
Journal:  J Neuromuscul Dis       Date:  2020

6.  Relationships between muscle size, strength, and physical activity in adults with muscular dystrophy.

Authors:  Matthew F Jacques; Gladys L Onambele-Pearson; Neil D Reeves; Georgina K Stebbings; Jonathon Smith; Christopher I Morse
Journal:  J Cachexia Sarcopenia Muscle       Date:  2018-10-19       Impact factor: 12.910

  6 in total

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