The instrumented timed up and go test: potential outcome measure for disease modifying therapies in Parkinson's disease

The Timed Up and Go (TUG) test has been used to assess balance and mobility in Parkinson's Disease (PD). However, it is not known if this test is sensitive to subtle abnormalities present in early stages of the disease, when balance and gait problems are not clinically evident but may be detect...

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Published inJournal of neurology, neurosurgery and psychiatry Vol. 81; no. 2; pp. 171 - 176
Main Authors Zampieri, Cris, Salarian, Arash, Carlson-Kuhta, Patricia, Aminian, Kamiar, Nutt, John G, Horak, Fay B
Format Journal Article
LanguageEnglish
Published London BMJ Publishing Group Ltd 01.02.2010
BMJ Publishing Group
BMJ Publishing Group LTD
Subjects
Online AccessGet full text
ISSN0022-3050
1468-330X
1468-330X
DOI10.1136/jnnp.2009.173740

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Abstract The Timed Up and Go (TUG) test has been used to assess balance and mobility in Parkinson's Disease (PD). However, it is not known if this test is sensitive to subtle abnormalities present in early stages of the disease, when balance and gait problems are not clinically evident but may be detected with instrumented analysis of movement. We hypothesise that postural transitions and arm swing during gait will be the most sensitive characteristics of the TUG for early PD. In the present study, we instrumented the TUG test (iTUG) using portable inertial sensors, and extended the walking distance from 3 m (traditional TUG) to 7 m. Twelve subjects with early-to-moderate, untreated PD and 12 healthy individuals participated. Our findings show that although the stopwatch measure of TUG duration did not detect any abnormalities in early-to-mid-stage PD, the peak arm swing velocity on the more affected side, average turning velocity, cadence and peak trunk rotation velocity were significantly slower. These iTUG parameters were also correlated with the Unified Parkinson's Disease Rating Motor Scale. Thus, the iTUG test is sensitive to untreated PD and could potentially detect progression of PD and response to symptomatic and disease-modifying treatments.
AbstractList The Timed Up and Go (TUG) test has been used to assess balance and mobility in Parkinson’s Disease (PD). However, it is not known if this test is sensitive to subtle abnormalities present in early stages of the disease, when balance and gait problems are not clinically evident but may be detected with instrumented analysis of movement. We hypothesize that postural transitions and arm swing during gait will be the most sensitive characteristics of the TUG for early PD. In the present study, we instrumented the TUG test (iTUG) using portable inertial sensors, and extended the walking distance from 3 meters (traditional TUG) to 7 meters. Twelve subjects with early-to-moderate, untreated PD and 12 healthy individuals participated. Our findings show that although the stopwatch measure of TUG duration did not detect abnormalities in early-to-mid stage PD, the peak arm swing velocity on the more affected side, average turning velocity, cadence and peak trunk rotation velocity were significantly slower. These iTUG parameters were also correlated with the UPDRS Motor Scale. Thus, the iTUG test is sensitive to untreated PD and could potentially detect progression of PD and response to symptomatic and disease-modifying treatments.
The Timed Up and Go (TUG) test has been used to assess balance and mobility in Parkinson's Disease (PD). However, it is not known if this test is sensitive to subtle abnormalities present in early stages of the disease, when balance and gait problems are not clinically evident but may be detected with instrumented analysis of movement. We hypothesise that postural transitions and arm swing during gait will be the most sensitive characteristics of the TUG for early PD. In the present study, we instrumented the TUG test (iTUG) using portable inertial sensors, and extended the walking distance from 3 m (traditional TUG) to 7 m. Twelve subjects with early-to-moderate, untreated PD and 12 healthy individuals participated. Our findings show that although the stopwatch measure of TUG duration did not detect any abnormalities in early-to-mid-stage PD, the peak arm swing velocity on the more affected side, average turning velocity, cadence and peak trunk rotation velocity were significantly slower. These iTUG parameters were also correlated with the Unified Parkinson's Disease Rating Motor Scale. Thus, the iTUG test is sensitive to untreated PD and could potentially detect progression of PD and response to symptomatic and disease-modifying treatments.The Timed Up and Go (TUG) test has been used to assess balance and mobility in Parkinson's Disease (PD). However, it is not known if this test is sensitive to subtle abnormalities present in early stages of the disease, when balance and gait problems are not clinically evident but may be detected with instrumented analysis of movement. We hypothesise that postural transitions and arm swing during gait will be the most sensitive characteristics of the TUG for early PD. In the present study, we instrumented the TUG test (iTUG) using portable inertial sensors, and extended the walking distance from 3 m (traditional TUG) to 7 m. Twelve subjects with early-to-moderate, untreated PD and 12 healthy individuals participated. Our findings show that although the stopwatch measure of TUG duration did not detect any abnormalities in early-to-mid-stage PD, the peak arm swing velocity on the more affected side, average turning velocity, cadence and peak trunk rotation velocity were significantly slower. These iTUG parameters were also correlated with the Unified Parkinson's Disease Rating Motor Scale. Thus, the iTUG test is sensitive to untreated PD and could potentially detect progression of PD and response to symptomatic and disease-modifying treatments.
The Timed Up and Go (TUG) test has been used to assess balance and mobility in Parkinson's Disease (PD). However, it is not known if this test is sensitive to subtle abnormalities present in early stages of the disease, when balance and gait problems are not clinically evident but may be detected with instrumented analysis of movement. We hypothesise that postural transitions and arm swing during gait will be the most sensitive characteristics of the TUG for early PD. In the present study, we instrumented the TUG test (iTUG) using portable inertial sensors, and extended the walking distance from 3 m (traditional TUG) to 7 m. Twelve subjects with early-to-moderate, untreated PD and 12 healthy individuals participated. Our findings show that although the stopwatch measure of TUG duration did not detect any abnormalities in early-to-mid-stage PD, the peak arm swing velocity on the more affected side, average turning velocity, cadence and peak trunk rotation velocity were significantly slower. These iTUG parameters were also correlated with the Unified Parkinson's Disease Rating Motor Scale. Thus, the iTUG test is sensitive to untreated PD and could potentially detect progression of PD and response to symptomatic and disease-modifying treatments.
Author Zampieri, Cris
Carlson-Kuhta, Patricia
Horak, Fay B
Salarian, Arash
Nutt, John G
Aminian, Kamiar
AuthorAffiliation 1 Balance Disorders Laboratory, Department of Neurology, School of Medicine, Oregon Health & Science University, 505 NW 185th Avenue, Beaverton, OR 97006, USA
2 Balance Disorders Laboratory, Department of Physiology and Pharmacology, School of Medicine, Oregon Health & Science University, 505 NW 185th Avenue, Beaverton, OR 97006, USA
3 Laboratory of Movement Analysis and Measurement, Ecole Polytechnique Fédéral de Lausanne, 1015 Lausanne, Switzerland
AuthorAffiliation_xml – name: 1 Balance Disorders Laboratory, Department of Neurology, School of Medicine, Oregon Health & Science University, 505 NW 185th Avenue, Beaverton, OR 97006, USA
– name: 3 Laboratory of Movement Analysis and Measurement, Ecole Polytechnique Fédéral de Lausanne, 1015 Lausanne, Switzerland
– name: 2 Balance Disorders Laboratory, Department of Physiology and Pharmacology, School of Medicine, Oregon Health & Science University, 505 NW 185th Avenue, Beaverton, OR 97006, USA
Author_xml – sequence: 1
  givenname: Cris
  surname: Zampieri
  fullname: Zampieri, Cris
  email: carlsonp@ohsu.edu
  organization: Balance Disorders Laboratory, Department of Neurology, School of Medicine, Oregon Health & Science University, Portland, Oregon, USA
– sequence: 2
  givenname: Arash
  surname: Salarian
  fullname: Salarian, Arash
  email: carlsonp@ohsu.edu
  organization: Laboratory of Movement Analysis and Measurement, Ecole Polytechnique Fédéral de Lausanne, Lausanne, Switzerland
– sequence: 3
  givenname: Patricia
  surname: Carlson-Kuhta
  fullname: Carlson-Kuhta, Patricia
  email: carlsonp@ohsu.edu
  organization: Balance Disorders Laboratory, Department of Neurology, School of Medicine, Oregon Health & Science University, Portland, Oregon, USA
– sequence: 4
  givenname: Kamiar
  surname: Aminian
  fullname: Aminian, Kamiar
  email: carlsonp@ohsu.edu
  organization: Laboratory of Movement Analysis and Measurement, Ecole Polytechnique Fédéral de Lausanne, Lausanne, Switzerland
– sequence: 5
  givenname: John G
  surname: Nutt
  fullname: Nutt, John G
  email: carlsonp@ohsu.edu
  organization: Balance Disorders Laboratory, Department of Physiology and Pharmacology, School of Medicine, Oregon Health & Science University, Portland, Oregon, USA
– sequence: 6
  givenname: Fay B
  surname: Horak
  fullname: Horak, Fay B
  email: carlsonp@ohsu.edu
  organization: Balance Disorders Laboratory, Department of Physiology and Pharmacology, School of Medicine, Oregon Health & Science University, Portland, Oregon, USA
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Copyright 2009, Published by the BMJ Publishing Group Limited For permission to use, (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.
2015 INIST-CNRS
Copyright: 2009 (c) 2009, Published by the BMJ Publishing Group Limited For permission to use, (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.
Copyright_xml – notice: 2009, Published by the BMJ Publishing Group Limited For permission to use, (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.
– notice: 2015 INIST-CNRS
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Issue 2
Keywords Nervous system diseases
Prognosis
Treatment
Central nervous system disease
Instrument
Parkinson disease
Degenerative disease
Cerebral disorder
Extrapyramidal syndrome
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Podsiadlo, Richardson 1991; 39
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Salarian, Russmann, Vingerhoets 2004; 51
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Snippet The Timed Up and Go (TUG) test has been used to assess balance and mobility in Parkinson's Disease (PD). However, it is not known if this test is sensitive to...
The Timed Up and Go (TUG) test has been used to assess balance and mobility in Parkinson’s Disease (PD). However, it is not known if this test is sensitive to...
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StartPage 171
SubjectTerms Aged
Algorithms
Antiparkinson Agents - therapeutic use
Biological and medical sciences
Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
Female
Gait
Humans
inertial sensors
Male
Medical sciences
Middle Aged
Mobility
Movement Disorders - diagnosis
Movement Disorders - epidemiology
Neurology
Parkinson Disease - diagnosis
Parkinson Disease - drug therapy
Parkinson Disease - epidemiology
Parkinson's disease
postural transitions
Posture
Psychomotor Performance
Range of motion
Sensors
Surveys and Questionnaires
Time Factors
timed up and go
Velocity
Title The instrumented timed up and go test: potential outcome measure for disease modifying therapies in Parkinson's disease
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Volume 81
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