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Evaluation of reliability and sensitivity of a new 6-minute walk test and pitch-up method for neuromuscular dystrophy

Research Project

Project/Area Number 16K01435
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Medical engineering assessment
Research InstitutionShinshu University

Principal Investigator

Nishizawa Hitomi  信州大学, 学術研究院保健学系, 助教 (90573379)

Co-Investigator(Kenkyū-buntansha) 柴 直子  信州大学, 医学部, 助教(特定雇用) (00639289)
中村 昭則  信州大学, 医学部, 特任教授 (10303471)
Project Period (FY) 2016-04-01 – 2019-03-31
Project Status Completed (Fiscal Year 2018)
Budget Amount *help
¥4,680,000 (Direct Cost: ¥3,600,000、Indirect Cost: ¥1,080,000)
Fiscal Year 2018: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2017: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2016: ¥2,730,000 (Direct Cost: ¥2,100,000、Indirect Cost: ¥630,000)
Keywords神経筋疾患 / 6分間歩行 / 再現性 / Duchenne型筋ジストロフィー / 6分間歩行 / DMD / 活動量 / 運動機能評価 / 6分間歩行試験 / 臨床的に意義のある最少変化量 / 臨床研究
Outline of Final Research Achievements

In walking distance, it was proved that the new 6 MWT (791.3 ± 61.3 m) was significantly longer (p <0.001) than the old 6 MWT (665.1 ± 73.8 m). The subjects were evaluated for riliability two types of six-minute walking. As a result, it was found that a high reproducibility of ICC = 0.8 was obtained. Furthermore, the minimum clinically relevant change (sensitivity) was calculated to be 9.2 m. From these facts, it is suggested that when performing a 6-minute walk test on patients with muscular dystrophy, it can be judged that the symptom has progressed when a walk distance of 9.2 m or more is shortened.

Academic Significance and Societal Importance of the Research Achievements

神経筋疾患の中でもDuchenne型筋ジストロフィーは幼少期より発症し,約13歳で歩行不能になると言われており,個人差はあるものの比較的早い時間で症状が進行する.歩行可能な時期のほとんどを小学校で過ごす彼らは,体育の授業や運動会,または友達との遊びの中で筋肉の炎症を起こすことで症状が進行する場合もある.その進行のわずかな変化を定期的な理学療法評価でとらえることができれば,家族や学校への助言も適格に行え,症状の悪化を防ぐことも可能となる.本研究の成果は,症状の悪化を防げる点,当事者や関係者に対して病状の説明を行う際,具体的に呈示することができる点に社会的意義があると考える.

Report

(4 results)
  • 2018 Annual Research Report   Final Research Report ( PDF )
  • 2017 Research-status Report
  • 2016 Research-status Report
  • Research Products

    (3 results)

All 2016

All Journal Article (1 results) (of which Peer Reviewed: 1 results,  Open Access: 1 results) Presentation (2 results)

  • [Journal Article] Usefulness of continual actigraph for assessing the effect of corticosteroid treatment to Duchenne muscular dystrophy: A case report2016

    • Author(s)
      Hitomi Nishizawa, Naoko Shiba, Akinori Nakamura
    • Journal Title

      Journal of Physical Therapy Science

      Volume: 28 Pages: 3249-3251

    • Related Report
      2016 Research-status Report
    • Peer Reviewed / Open Access
  • [Presentation] 神経筋疾患患者における従来の運動機能評価法と日常活動量との関連の検討2016

    • Author(s)
      西澤公美
    • Organizer
      小牧班会議
    • Place of Presentation
      東京JA共済ビルカンファレンスホール
    • Year and Date
      2016-11-26
    • Related Report
      2016 Research-status Report
  • [Presentation] Duchenne型筋ジストロフィー患児を対象とした新しい6分間歩行試験の開発2016

    • Author(s)
      西澤公美
    • Organizer
      第57回日本神経学会学術大会
    • Place of Presentation
      神戸国際会議場
    • Year and Date
      2016-05-18
    • Related Report
      2016 Research-status Report

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Published: 2016-04-21   Modified: 2020-03-30  

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