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June 05, 2007; 68 (23) Articles

A randomized controlled trial of resistance exercise in individuals with ALS

V. Dal Bello-Haas, J. M. Florence, A. D. Kloos, J. Scheirbecker, G. Lopate, S. M. Hayes, E. P. Pioro, H. Mitsumoto
First published June 4, 2007, DOI: https://doi.org/10.1212/01.wnl.0000264418.92308.a4
V. Dal Bello-Haas
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A. D. Kloos
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Citation
A randomized controlled trial of resistance exercise in individuals with ALS
V. Dal Bello-Haas, J. M. Florence, A. D. Kloos, J. Scheirbecker, G. Lopate, S. M. Hayes, E. P. Pioro, H. Mitsumoto
Neurology Jun 2007, 68 (23) 2003-2007; DOI: 10.1212/01.wnl.0000264418.92308.a4

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Abstract

Objective: To determine the effects of resistance exercise on function, fatigue, and quality of life in individuals with ALS.

Methods: Subjects with a diagnosis of clinically definite, probable, or laboratory-supported ALS, forced vital capacity (FVC) of 90% predicted or greater, and an ALS Functional Rating Scale (ALSFRS) score of 30 or greater were randomly assigned to a resistance exercise group that received a home exercise program consisting of daily stretching and resistance exercises three times weekly or to a usual care group, who performed only the daily stretching exercises. ALSFRS, the Fatigue Severity Scale (FSS), and Short Form-36 (SF-36) were completed at baseline and monthly for 6 months. FVC and maximum voluntary isometric contraction (MVIC) were monitored monthly throughout the study.

Results: Of 33 subjects screened, 27 were randomly assigned (resistance = 13; usual care = 14). Eight resistance exercise subjects and 10 usual care subjects completed the trial. At 6 months, the resistance exercise group had significantly higher ALSFRS and SF-36 physical function subscale scores. No adverse events related to the intervention occurred, MVIC and FVC indicated no negative effects, and less decline in leg strength measured by MVIC was found in the resistance exercise group.

Conclusion: Our study, although small, showed that the resistance exercise group had significantly better function, as measured by total ALS Functional Rating Scale and upper and lower extremity subscale scores, and quality of life without adverse effects as compared with subjects receiving usual care.

Footnotes

  • Supplemental data at www.neurology.org

    Funded in part by the Amyotrophic Lateral Sclerosis Association (Clinical Management Research Grant Program), Calabasas Hills, CA.

    Disclosure: The authors report no conflicts of interest.

    Received September 7, 2006. Accepted in final form February 2, 2007.

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Letters: Rapid online correspondence

  • A randomized controlled trial of resistance exercise in individuals with ALS
    • Carmel Armon, M.D., M.H.S., Baystate Medical Center, 759 Chestnut Street - S4648, Springfield, MA 01199Carmel.Armon@bhs.org
    Submitted February 25, 2008
  • Reply from the authors
    • Vanina PM Dal Bello-Haas, School of Physical Therapy, University of Saskatchewan, 1121 College Drive, Saskatoon, SK S7N 0W3vanina.dalbello-haas@usask.ca
    • Julaine M Florence, Anne D Kloos, Jeanine Scheirbecker, Glenn Lopate, Sheila M Hayes, Erik P Pioro, Hiroshi Mitsumoto
    Submitted February 25, 2008
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