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Motor Performance in South African Children with Cystic Fibrosis
Aims: This study aimed to investigate motor performance in children with cystic fibrosis (CF) and the relationship with respiratory and anthropometric outcome measures. Methods: A cross-sectional exploratory study investigated 12 children with CF, mean (SD) age 6.17 (0.67) years, using the Movement...
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Published in: | Physical & occupational therapy in pediatrics 2020-03, Vol.40 (2), p.192-200 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Aims: This study aimed to investigate motor performance in children with cystic fibrosis (CF) and the relationship with respiratory and anthropometric outcome measures.
Methods: A cross-sectional exploratory study investigated 12 children with CF, mean (SD) age 6.17 (0.67) years, using the Movement Assessment Battery for Children 2nd edition (MABC-2), spirometry, body weight, height, body mass index, and age-related anthropomorphic z-scores.
Results: MABC-2 total scores indicated 9/12 (75%) children performed below average ( |
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ISSN: | 0194-2638 1541-3144 |
DOI: | 10.1080/01942638.2019.1647329 |