• Title of article

    Verification of a Motion Sensor for Evaluating Physical Activity in COPD Patients

  • Author/Authors

    Miyamoto, Seiko Department of Clinical Laboratory - National Hospital Organization Wakayama Hospital, Wada Mihama-cho, Wakayama, Japan , Minakata, Yoshiaki Department of Clinical Laboratory - National Hospital Organization Wakayama Hospital, Wada Mihama-cho, Wakayama, Japan , Azuma, Yuichiro Department of Clinical Laboratory - National Hospital Organization Wakayama Hospital, Wada Mihama-cho, Wakayama, Japan , Kawabe, Kazumi Department of Clinical Laboratory - National Hospital Organization Wakayama Hospital, Wada Mihama-cho, Wakayama, Japan , Ono, Hideya Department of Clinical Laboratory - National Hospital Organization Wakayama Hospital, Wada Mihama-cho, Wakayama, Japan , Yanagimoto, Ryuta Department of Clinical Laboratory - National Hospital Organization Wakayama Hospital, Wada Mihama-cho, Wakayama, Japan , Suruda, Tadatoshi Department of Clinical Laboratory - National Hospital Organization Wakayama Hospital, Wada Mihama-cho, Wakayama, Japan

  • Pages
    9
  • From page
    1
  • To page
    9
  • Abstract
    Background. Objective evaluation of the physical activity (PA) in patients with chronic obstructive pulmonary disease (COPD) is important. We validated a triaxial accelerometer, Active Style Pro HJA-750C® (HJA), and evaluated the necessary conditions for obtaining reproducible data. Methods. The PA measured by HJA was compared with that measured by two already validated accelerometers in 11 patients with COPD (age: 76.6 ± 6.9, FEV1% predicted: 57.6 ± 18.6). Then, the influence of weather and holidays on the PA and the required number of days to obtain repeatability were examined in 21 patients with COPD (age: 73.0 ± 8.0, FEV1% predicted: 58.7 ± 19.0). Results. +e PA values measured by HJA and those by DynaPort Move Monitor® (DMM) or Actimarker® (AM) were significantly correlated at all intensities (p = 0.024 at ≥4.0 METs by DMM and p < 0.0001 at the rest) except at ≥4.0 METs by AM, though the values measured by HJA were higher than those by AM which was reported to underestimate PA. The durations of PA on rainy days were significantly shorter than those on nonrainy days, but those on holidays were not different from those on weekdays. The values of ICC for 3, 4, or 5 days were higher than 0.8 at all intensities. The PA measured by HJA was correlated with the dyspnea scale FVC and age and tended to correlate with FEV1. Conclusions. The HJA was validated for evaluating the PA in patients with COPD. This trial is registered with UMIN000016363.
  • Keywords
    Motion Sensor , Evaluating Physical , COPD Patients
  • Journal title
    Canadian Respiratory Journal
  • Serial Year
    2018
  • Record number

    2605694