Long-term unsupervised mobility assessment in movement disorders. Warmerdam, E., Hausdorff, J. M, Atrsaei, A., Zhou, Y., Mirelman, A., Aminian, K., Espay, A. J, Hansen, C., Evers, L. J W, Keller, A., Lamoth, C., Pilotto, A., Rochester, L., Schmidt, G., Bloem, B. R, & Maetzler, W. The Lancet Neurology, 02, 2020.
doi  abstract   bibtex   1 download  
Mobile health technologies (wearable, portable, body-fixed sensors, or domestic-integrated devices) that quantify mobility in unsupervised, daily living environments are emerging as complementary clinical assessments. Data collected in these ecologically valid, patient-relevant settings can overcome limitations of conventional clinical assessments, as they capture fluctuating and rare events. These data could support clinical decision making and could also serve as outcomes in clinical trials. However, studies that directly compared assessments made in unsupervised and supervised (eg, in the laboratory or hospital) settings point to large disparities, even in the same parameters of mobility. These differences appear to be affected by psychological, physiological, cognitive, environmental, and technical factors, and by the types of mobilities and diagnoses assessed. To facilitate the successful adaptation of the unsupervised assessment of mobility into clinical practice and clinical trials, clinicians and researchers should consider these disparities and the multiple factors that contribute to them.
@Article{e2020,
  author       = {Warmerdam, Elke and Hausdorff, Jeffrey M and Atrsaei, Arash and Zhou, Yuhan and Mirelman, Anat and Aminian, Kamiar and Espay, Alberto J and Hansen, Clint and Evers, Luc J W and Keller, Andreas and Lamoth, Claudine and Pilotto, Andrea and Rochester, Lynn and Schmidt, Gerhard and Bloem, Bastiaan R and Maetzler, Walter },
  title        = {Long-term unsupervised mobility assessment in movement disorders},
  journal      = {The Lancet Neurology},
  year         = {2020},
  month        = {02},
  pages        = {1474-4422},
  abstract     = {Mobile health technologies (wearable, portable, body-fixed sensors, or domestic-integrated devices) that quantify mobility in unsupervised, daily living environments are emerging as complementary clinical assessments. Data collected in these ecologically valid, patient-relevant settings can overcome limitations of conventional clinical assessments, as they capture fluctuating and rare events. These data could support clinical decision making and could also serve as outcomes in clinical trials. However, studies that directly compared assessments made in unsupervised and supervised (eg, in the laboratory or hospital) settings point to large disparities, even in the same parameters of mobility. These differences appear to be affected by psychological, physiological, cognitive, environmental, and technical factors, and by the types of mobilities and diagnoses assessed. To facilitate the successful adaptation of the unsupervised assessment of mobility into clinical practice and clinical trials, clinicians and researchers should consider these disparities and the multiple factors that contribute to them.},
  doi          = {10.1016/S1474-4422(19)30397-7},
  pii          = {10.1016/S1474-4422(19)30397-7},
}

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