Quantitative clinical assessment of motor function during and following LSVT-BIG® therapy.
Accelerometry
Exercise therapy
Finger tapping
Gait analysis
Lee Silverman voice therapy
Parkinson’s disease
Postural control
Sit-to-stand
Timed-up-and-go
Wearable sensors
Journal
Journal of neuroengineering and rehabilitation
ISSN: 1743-0003
Titre abrégé: J Neuroeng Rehabil
Pays: England
ID NLM: 101232233
Informations de publication
Date de publication:
13 07 2020
13 07 2020
Historique:
received:
24
10
2019
accepted:
08
07
2020
entrez:
15
7
2020
pubmed:
15
7
2020
medline:
16
12
2020
Statut:
epublish
Résumé
LSVT-BIG® is an intensively delivered, amplitude-oriented exercise therapy reported to improve mobility in individuals with Parkinson's disease (PD). However, questions remain surrounding the efficacy of LSVT-BIG® when compared with similar exercise therapies. Instrumented clinical tests using body-worn sensors can provide a means to objectively monitor patient progression with therapy by quantifying features of motor function, yet research exploring the feasibility of this approach has been limited to date. The aim of this study was to use accelerometer-instrumented clinical tests to quantify features of gait, balance and fine motor control in individuals with PD, in order to examine motor function during and following LSVT-BIG® therapy. Twelve individuals with PD undergoing LSVT-BIG® therapy, eight non-exercising PD controls and 14 healthy controls were recruited to participate in the study. Functional mobility was examined using features derived from accelerometry recorded during five instrumented clinical tests: 10 m walk, Timed-Up-and-Go, Sit-to-Stand, quiet stance, and finger tapping. PD subjects undergoing therapy were assessed before, each week during, and up to 13 weeks following LSVT-BIG®. Accelerometry data captured significant improvements in 10 m walk and Timed-Up-and-Go times with LSVT-BIG® (p < 0.001), accompanied by increased stride length. Temporal features of the gait cycle were significantly lower following therapy, though no change was observed with measures of asymmetry or stride variance. The total number of Sit-to-Stand transitions significantly increased with LSVT-BIG® (p < 0.001), corresponding to a significant reduction of time spent in each phase of the Sit-to-Stand cycle. No change in measures related to postural or fine motor control was observed with LSVT-BIG®. PD subjects undergoing LSVT-BIG® showed significant improvements in 10 m walk (p < 0.001) and Timed-Up-and-Go times (p = 0.004) over a four-week period when compared to non-exercising PD controls, who showed no week-to-week improvement in any task examined. This study demonstrates the potential for wearable sensors to objectively quantify changes in motor function in response to therapeutic exercise interventions in PD. The observed improvements in accelerometer-derived features provide support for instrumenting gait and sit-to-stand tasks, and demonstrate a rescaling of the speed-amplitude relationship during gait in PD following LSVT-BIG®.
Sections du résumé
BACKGROUND
LSVT-BIG® is an intensively delivered, amplitude-oriented exercise therapy reported to improve mobility in individuals with Parkinson's disease (PD). However, questions remain surrounding the efficacy of LSVT-BIG® when compared with similar exercise therapies. Instrumented clinical tests using body-worn sensors can provide a means to objectively monitor patient progression with therapy by quantifying features of motor function, yet research exploring the feasibility of this approach has been limited to date. The aim of this study was to use accelerometer-instrumented clinical tests to quantify features of gait, balance and fine motor control in individuals with PD, in order to examine motor function during and following LSVT-BIG® therapy.
METHODS
Twelve individuals with PD undergoing LSVT-BIG® therapy, eight non-exercising PD controls and 14 healthy controls were recruited to participate in the study. Functional mobility was examined using features derived from accelerometry recorded during five instrumented clinical tests: 10 m walk, Timed-Up-and-Go, Sit-to-Stand, quiet stance, and finger tapping. PD subjects undergoing therapy were assessed before, each week during, and up to 13 weeks following LSVT-BIG®.
RESULTS
Accelerometry data captured significant improvements in 10 m walk and Timed-Up-and-Go times with LSVT-BIG® (p < 0.001), accompanied by increased stride length. Temporal features of the gait cycle were significantly lower following therapy, though no change was observed with measures of asymmetry or stride variance. The total number of Sit-to-Stand transitions significantly increased with LSVT-BIG® (p < 0.001), corresponding to a significant reduction of time spent in each phase of the Sit-to-Stand cycle. No change in measures related to postural or fine motor control was observed with LSVT-BIG®. PD subjects undergoing LSVT-BIG® showed significant improvements in 10 m walk (p < 0.001) and Timed-Up-and-Go times (p = 0.004) over a four-week period when compared to non-exercising PD controls, who showed no week-to-week improvement in any task examined.
CONCLUSIONS
This study demonstrates the potential for wearable sensors to objectively quantify changes in motor function in response to therapeutic exercise interventions in PD. The observed improvements in accelerometer-derived features provide support for instrumenting gait and sit-to-stand tasks, and demonstrate a rescaling of the speed-amplitude relationship during gait in PD following LSVT-BIG®.
Identifiants
pubmed: 32660495
doi: 10.1186/s12984-020-00729-8
pii: 10.1186/s12984-020-00729-8
pmc: PMC7359464
doi:
Types de publication
Clinical Study
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
92Références
Mov Disord. 2011 Aug 1;26(9):1605-15
pubmed: 21674624
Clin Rehabil. 2018 Sep;32(9):1284-1285
pubmed: 29644881
Mov Disord. 2013 Sep 15;28(11):1544-51
pubmed: 24132842
J Neurol Phys Ther. 2016 Jan;40(1):3-14
pubmed: 26655098
Exp Brain Res. 2007 Mar;177(3):336-46
pubmed: 16972073
J Neuroeng Rehabil. 2005 Jul 31;2:23
pubmed: 16053531
J Gerontol A Biol Sci Med Sci. 2009 Jun;64(6):700-6
pubmed: 19221191
PLoS One. 2017 Oct 11;12(10):e0183989
pubmed: 29020012
Parkinsons Dis. 2015;2015:586378
pubmed: 25722915
Am J Occup Ther. 2014 Jan-Feb;68(1):39-49
pubmed: 24367954
Exp Brain Res. 2005 Dec;167(3):462-7
pubmed: 16283401
J Gerontol A Biol Sci Med Sci. 2019 Mar 14;74(4):500-506
pubmed: 29300849
Clin Rehabil. 2018 May;32(5):607-618
pubmed: 28980476
J Neurosci. 1986 Nov;6(11):3309-18
pubmed: 3772433
J Neurol Sci. 2003 Aug 15;212(1-2):47-53
pubmed: 12809998
IEEE Trans Neural Syst Rehabil Eng. 2013 Jul;21(4):664-73
pubmed: 23292821
J Neuroeng Rehabil. 2012 Oct 07;9:75
pubmed: 23039219
Gait Posture. 2013 Sep;38(4):1021-5
pubmed: 23791781
PLoS One. 2016 Mar 21;11(3):e0151881
pubmed: 26999051
Parkinsonism Relat Disord. 2018 Jan;46 Suppl 1:S53-S56
pubmed: 28760593
J Neural Transm (Vienna). 2015 Feb;122(2):253-6
pubmed: 24872078
PLoS One. 2017 Apr 27;12(4):e0175559
pubmed: 28448509
Phys Ther. 2014 Jul;94(7):1014-23
pubmed: 24557655
Brain. 1976 Jun;99(2):269-310
pubmed: 990899
Semin Speech Lang. 2006 Nov;27(4):283-99
pubmed: 17117354
Rehabil Res Pract. 2017;2017:9871070
pubmed: 28331638
Exp Brain Res. 1978 Jan 18;31(1):1-12
pubmed: 639903
Cochrane Database Syst Rev. 2007 Jul 18;(3):CD002813
pubmed: 17636709
Gait Posture. 2011 Apr;33(4):594-9
pubmed: 21333541
Med Eng Phys. 2010 Mar;32(2):119-25
pubmed: 19942472
Conf Proc IEEE Eng Med Biol Soc. 2019 Jul;2019:4596-4599
pubmed: 31946888
Exp Brain Res. 2014 Feb;232(2):713-21
pubmed: 24292517
J Biomech. 2004 Jan;37(1):121-6
pubmed: 14672575
Med Eng Phys. 2015 Apr;37(4):400-7
pubmed: 25749552
Mov Disord. 2001 Nov;16(6):1048-65
pubmed: 11748736
Gait Posture. 2018 May;62:468-474
pubmed: 29674286
Arch Phys Med Rehabil. 2014 May;95(5):996-9
pubmed: 24231400
IEEE J Biomed Health Inform. 2016 May;20(3):838-847
pubmed: 25850097
Brain. 1994 Oct;117 ( Pt 5):1169-81
pubmed: 7953597
Biol Psychiatry. 1998 Oct 15;44(8):775-7
pubmed: 9798082
IEEE Trans Neural Syst Rehabil Eng. 2010 Jun;18(3):303-10
pubmed: 20388604
IEEE Trans Inf Technol Biomed. 2011 May;15(3):481-90
pubmed: 21349795
Parkinsonism Relat Disord. 2011 Aug;17(7):557-62
pubmed: 21641263
Am J Occup Ther. 1985 Jun;39(6):386-91
pubmed: 3160243
PLoS One. 2016 Jul 08;11(7):e0157968
pubmed: 27391082
J Neuroeng Rehabil. 2016 May 12;13(1):46
pubmed: 27175731
Nat Rev Neurol. 2017 Nov;13(11):689-703
pubmed: 29027544
Eur J Neurosci. 2005 Sep;22(5):1248-56
pubmed: 16176368
IEEE Trans Biomed Eng. 2020 Mar;67(3):658-666
pubmed: 31150328
Clin Biomech (Bristol, Avon). 1998 Jun;13(4-5):320-327
pubmed: 11415803
Parkinsons Dis. 2012;2012:391946
pubmed: 22530161
J Phys Ther Sci. 2018 Apr;30(4):636-641
pubmed: 29706722
Mov Disord. 2010 Sep 15;25(12):1902-8
pubmed: 20669294
IEEE Trans Neural Syst Rehabil Eng. 2014 Sep;22(5):1064-71
pubmed: 24760912