Continuous monitoring and quantification of multiple parameters of daily physical activity in ambulatory Duchenne muscular dystrophy patients
Multiple motor function and strength assessment tools exist for the evaluation of neuromuscular diseases, but most do not directly assess functional ability in the patients' daily physical activity in their home environment. In this study our aim was to assess: 1) the feasibility and accuracy of physical activity monitoring during two days in a home environment of five DMD patients using a non-commercialized monitor containing a 3D accelerometer and a gyroscope, 2) if a difference in the physical activity parameters could be measured before and one month after starting prednisolone. We reliably quantified the time spend sitting, standing, lying, walking, the number of steps taken, the cadence, the number of walking episodes and their duration as well as how these were distributed over the day. Parameters possibly reflecting endurance, such as the duration of the walking episodes or the succession of two or three walking episodes lasting more than 30 s were the most improved after prednisolone treatment. This degree of detailed determination of physical activity in a home environment has not been previously reported in neuromuscular disorders to our knowledge and some of the reported parameters are potential new outcome measures in clinical trials. (C) 2010 European Paediatric Neurology Society. Published by Elsevier Ltd. All rights reserved.
Keywords: Duchenne muscular dystrophy ; Physical activity ; Motor function ; Accelerometer ; Gyroscope ; Six minute walk test ; Outcome measure ; Parkinsons-Disease ; Long-Term ; Children ; Accelerometry ; Healthy ; Ability ; System ; Scale ; Boys
Record created on 2010-08-31, modified on 2016-08-08