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    Rett syndrome: Establishing a novel outcome measure for walking activity in an era of clinical trials for rare disorders

    230260_230260 Main.pdf (533.0Kb)
    Access Status
    Open access
    Authors
    Downs, Jennepher
    Leonard, H.
    Jacoby, P.
    Brisco, L.
    Baikie, G.
    Hill, Kylie
    Date
    2015
    Type
    Journal Article
    
    Metadata
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    Citation
    Downs, J. and Leonard, H. and Jacoby, P. and Brisco, L. and Baikie, G. and Hill, K. 2015. Rett syndrome: Establishing a novel outcome measure for walking activity in an era of clinical trials for rare disorders. Disability and Rehabilitation. 37 (21): pp. 1992-1996.
    Source Title
    Disability and Rehabilitation
    DOI
    10.3109/09638288.2014.993436
    ISSN
    0963-8288
    School
    School of Physiotherapy and Exercise Science
    Remarks

    This is an Author's Original Manuscript of an article published by Taylor & Francis in Disability and Rehabilitation on 15/12/2014 available online at <a href="http://www.tandfonline.com/10.3109/09638288.2014.993436">http://www.tandfonline.com/10.3109/09638288.2014.993436</a>

    URI
    http://hdl.handle.net/20.500.11937/28124
    Collection
    • Curtin Research Publications
    Abstract

    Background: Rett syndrome is a pervasive neurological disorder with impaired gait as one criterion. This study investigated the capacity of three accelerometer-type devices to measure walking activity in Rett syndrome. Methods: Twenty-six participants (mean 18 years, SD 8) wore an Actigraph, ActivPAL and StepWatch Activity Monitor (SAM) during a video-taped session of activities. Agreement was determined between step-counts derived from each accelerometer and observation. Repeatability of SAM-derived step counts was determined using pairs of one-minute epochs during which the same participant was observed to walk with the same cadence. Results: The mean difference (limit of agreement) for the Actigraph, ActivPAL and SAM were −41 (SD 33), −16 (SD 21) and −1 (SD 16) steps/min, respectively. Agreement was influenced by a device/cadence interaction (p < 0.001) with greater under-recording at higher cadences. For SAM data, repeatability of step-count pairs was excellent (intraclass correlation coefficient 0.91, 95% CI 0.79–0.96). The standard error of measurement was 6 steps/min and we would be 95% confident that a change ≥17 steps/min would be greater than within-subject measurement error. Conclusions: The capacity of the SAM to measure physical activity in Rett syndrome allows focus on participation-based activities in clinical practice and clinical trials.

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