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(2013) Impact of cognitive training on balance and gait in olderadults. Journals of Gerontology, Series B:
Psychological Sciences and Social Sciences, doi:10.1093/geronb/gbt097
Method. This randomized trial tested whether cognitive training over 10 weeks improves balance and gait in older
adults. Participants were randomly assigned to a computer-based cognitive training intervention or measurement-only
control. Outcomes included Timed Up and Go (TUG), gait speed, and gait speed with a cognitive distraction. Data were
analyzed using analysis of covariance models with change scores.
Results. Participants (N=51) average age was 82.7 for those randomized to intervention and 81.1 for those randomized to control. After 10 weeks, intervention group participants performed significantly better than controls on the
TUG. When the cohort was limited to those categorized as slow walkers (baseline 10-m walk 9 s), intervention participants performed significantly better than controls on TUG and distracted walking.
Discussion. Cognitive training slows degradation of balance and improves gait while distracted, rendering it a promising approach to falls prevention.
Key Words: BalanceCognitive trainingFallsGaitOlder adults.
The Author 2013. Published by Oxford University Press on behalf of The Gerontological Society of America.
All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.
Received February 5, 2013; Accepted August 5, 2013
Decision Editor: Myra Fernandes, PhD
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Objectives. Cognitive processing plays an important role in balance and gait and is a contributing factor to falls in
older adults. This relationship may be explained by the fact that higher order cognitive functions such as executive functions are called upon while walking. The purpose of this study was to examine whether a cognitive training intervention
leads to significant improvements on measures of balance and gait.
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Smith-Ray etal.
Figure1. Conceptual model of the association between cognitive training and falls.
Procedure
Participants were recruited from Chicago-area Inde
pendent Living facilities through presentations by the
principal investigator, study advertisements printed in
program guides, study advertisements posted on closed
broadcast television stations within the Independent Living
facilities, internal mailings of study recruitment flyers to
Independent Living facility residents, and through flyers
posted throughout each facility. This study was approved
by the University of Illinois at Chicago Institutional Review
Board (2010-0042).
Participants were randomized into one of two study arms
immediately after consenting to participatethe intervention arm or a control arm. Researchers were not blinded to
study arm condition; however, potential bias was minimal
because the outcomes of interestbalance and gaitwere
measured quantitatively with little room for subjectivity on
behalf of the researcher. Outcomes were assessed at baseline and immediately posttraining (10 weeks) through individual interviews administered by researchstaff.
Control condition.Participants randomized to the control arm received materials on preventing falls. At the conclusion of the baseline data collection session, participants
assigned to the control arm were given two brochures on
fall prevention for older adults produced by the Centers for
Disease Control and Prevention. Control arm participants
were contacted by study staff intermittently to inquire about
recent fall incidents or concerns. At the end of the study
period, control participants were offered a copy of the cognitive training program at no charge so that they could also
receive the potential benefits of cognitive training.
Intervention condition.Each participant in the intervention arm was exposed to the computer-based cognitive
training program. The majority of participants (four of five
facilities) completed the intervention in a class-based format
Participants
Participants were males and females aged 70 years or
older. Inclusion criteria were (a) at least one self-reported
fall within the last 2years or a self-reported balance impairment, (b) aged 70 or older, and (c) score of greater than or
equal to 26 on the Mini-Mental State Examination (Folstein,
Folstein, & McHugh, 1975). Exclusion criteria were (a)
presence of a severe walking or balance impairment, (b)
previously completed a cognitive training program within
the last year, (c) colorblindness, (d) plans to begin a balance
program during the study period, (e) self-reported presence of vertigo, (f) visual acuity of less than 20/80, or (g)
currently using psychotropic medications.
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Smith-Ray etal.
Measures.At baseline, participants completed a questionnaire that included psychometric evaluation of executive
functions, including visuospatial working memory, inhibition, attention, age, sex, gender, instrumental activities of
daily living (IADL), medical conditions, and physical and
social activities. Participants were screened for depression
using the short-form Geriatric Depression Scale (Sheikh
& Yesavage, 1986). Participants who scored 6 or above on
the scale were provided with names of local providers who
could help diagnose and treat depression. Demographic
data included age, gender, race/ethnicity, and years of education, and health data included activities of daily living,
IADL, physician-diagnosed chronic health conditions, and
current medications.
Balance was measured using the number of seconds to
complete the Timed Up and Go (TUG) test (Steffen, Hacker,
& Mollinger, 2002; van Hedel, Wirz, & Dietz, 2005). Gait
speed was measured during a simple indoor walking course
that involved walking 10 m at a usual or comfortable pace.
Time to complete the 10-m walk test is a sensitive measure
of gait abnormalities (van Hedel et al., 2005). The 10-m
walk was completed 3 times and the average (seconds) of
these three performances was used for the analysis. After
this, the 10-m walk test was completed 3 more times while
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for the primary outcomes of balance and gait: (a) intent-totreat analysis and (b) an analysis that was limited to participants who were categorized as slow walkers based on gait
speed at baseline. Cohens d effect sizes were calculated
to determine the strength of the association between the
study arm and TUG, gait speed, and distracted gait speed.
Analyses were completed by study arm as randomized.
Intent-to-Treat Analysis
Timed Up and Go.The ANCOVA analyses found
a significant association between TUG and study arm
(F (2,36) = 4.47, p = .036). Mean TUG speed increased
for participants in both study groups between baseline
and postintervention, indicating that participants performance declined (i.e., became slower) between baseline
to 10 weeks. This performance decline was significantly
greater for control participants (=2.65) relative to intervention participants (=0.55; Figure2). The magnitude
of the effect between groups for TUG was large (Cohens
d=0.73). (Refer to Table2 for a complete summary of the
results.)
Gait speed.The ANCOVA model exhibited no significant association between groups on 10-m gait speed. Mean
number of seconds to complete the 10-m walk increased
Recruited/randomized
Dropped
Lost to follow-up
Completed study
Age (mean)
Gender (female)
Race
White
Black
Ethnicity (Hispanic origin)
Years of education
Depression score, mean (range:
0=low to 15=high)
MMSE score, mean (range: 0=low to
30=high)
IADL total, mean (range: 8=
independent to 31=dependent)
10-m walk (s)
10-m walk distracted (s)
Timed Up and Go (s)
Slow walkers (9 s on 10-m walk)
Intervention
Difference at
baseline
Control
N/Mean
Percent/SD
N/Mean
Percent/SD
N/Mean
Percent/SD
51
2
2
47
81.96
39
3.9%
3.9%
92.2%
6.36 SD
76.5%
27
1
0
26
82.73
21
3.7%
0.0%
96.3%
5.99 SD
77.8%
24
1
2
21
81.13
18
4.2%
8.3%
87.5%
6.77 SD
75.0%
48
2
1
15.26
94.1%
3.9%
2.0%
3.13 SD
24
2
0
14.92
88.9%
7.4%
0
2.88 SD
24
0
1
15.63
100.0%
0.0%
4.2%
3.40 SD
0.934
0.131
0.252
0.326
0.463
0.202
0.271
0.210
1.76
2.01 SD
2.1
2.19 SD
1.46
1.84 SD
0.154
28.4
2.00 SD
27.79
2.54 SD
28.75
1.11 SD
0.156
9.4
2.85 SD
9.63
3.29 SD
9.52
2.62 SD
0.710
11.10
12.89
11.26
33
3.04
3.33
4.36
64.7%
11.09
13.09
11.02
15
2.91
3.41
3.98
62.5%
11.12
12.67
11.52
18
3.25
3.32
4.80
66.7%
()
0.886
0.373
0.797
0.674
Results
A total of 53 participants were recruited into the study.
Of the 53, two were ineligible after prescreening due to a
severe hearing impairment (N = 1) and a severe balance
impairment (N=1). Two participants dropped study participation (3.9%), and two were lost to follow-up (3.9%). There
were no significant differences in attrition between groups
(Table 1). Of the 51 participants in the final cohort (27
intervention and 24 control), 47 participants (92.2%) completed baseline and follow-up measures, 26 (96.3%) in the
intervention and 21 (87.5%) in the control arm. Participants
who completed the study were similar to those who did
not complete the study in key characteristics including age
(mean 81.7years for completers, 81.8 for noncompleters),
race (96.0% vs 100% white), ethnicity (98.0% non-Hispanic vs 100% non-Hispanic), and depression (1.86 vs
1.75). However, those who completed the study were less
likely to be women (78.0% women vs 100% women) and
had slightly more education (15.3 grades complete vs 13.5
grades complete) than those that did not complete the study.
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Smith-Ray etal.
Table2. Output From ANCOVA Models Assessing the Association Between Outcomes and Treatment Arm
Intent-to-treat analysis
Control
change score
Intervention
change score
Control
change score
Intervention
change score
Mean
SD
Mean
SD
Cohens d
F Value
p Value
Mean
SD
Mean
SD
Cohens d
F Value
p Value
0.95
1.07
1.62
1.51
0.18
0.27
1.60
2.13
0.48
0.43
2.46
1.73
.124
.195
29
27
1.05
1.52
1.96
1.68
0.01
0.10
1.70
2.03
0.58
0.87
2.59
5.26
.120
.031*
2.65
3.46
0.55
2.13
0.73
4.74
.036*
23
3.91
3.47
0.88
2.40
1.02
5.37
.031*
Figure2. Mean differences on Timed Up and Go (TUG) for two analytic cohorts.
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Smith-Ray etal.
Funding
This project described was supported by the Agency for Healthcare
Research and Quality (AHRQ R36 HS18295) and the National Institute on
Aging through a dissertation award from the Midwest Roybal Center for
Health Promotion and Translation (P30AG022849).
Acknowledgments
Dr. R.L. Smith-Ray is grateful for the insight and guidance provided
by members of her dissertation committee including Drs. Hughes (Chair),
Prohaska, Hedeker, Little, and Jurivich. The content is solely the responsibility of the authors and does not necessarily represent the official views
of the National Institutes on Aging, the National Institutes of Health, or the
Agency for Healthcare Research and Quality.
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Correspondence
Correspondence should be addressed to Renae L. Smith-Ray, PhD,
Institute for Health Research and Policy, University of Illinois at Chicago,
1747W Roosevelt Road, Suite 558, Chicago, IL 60608. E-mail: rsmith27@
uic.edu.
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