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. 2022 Aug 3;17(8):e0269398. doi: 10.1371/journal.pone.0269398

Dividing attention during the Timed Up and Go enhances associations of several subtask performances with MCI and cognition

Victoria N Poole 1,2,*, Robert J Dawe 1,3, Melissa Lamar 1,4, Michael Esterman 5,6, Lisa Barnes 1,4,7, Sue E Leurgans 1,7,8, David A Bennett 1,7, Jeffrey M Hausdorff 1,2,9,10, Aron S Buchman 1,7
Editor: Eric R Anson11
PMCID: PMC9348700  PMID: 35921260

Abstract

We tested the hypothesis that dividing attention would strengthen the ability to detect mild cognitive impairment (MCI) and specific cognitive abilities from Timed Up and Go (TUG) performance in the community setting. While wearing a belt-worn sensor, 757 dementia-free older adults completed TUG during two conditions, with and without a concurrent verbal serial subtraction task. We segmented TUG into its four subtasks (i.e., walking, turning, and two postural transitions), and extracted 18 measures that were summarized into nine validated sensor metrics. Participants also underwent a detailed cognitive assessment during the same visit. We then employed a series of regression models to determine the combinations of subtask sensor metrics most strongly associated with MCI and specific cognitive abilities for each condition. We also compared subtask performances with and without dividing attention to determine whether the costs of divided attention were associated with cognition. While slower TUG walking and turning were associated with higher odds of MCI under normal conditions, these and other subtask associations became more strongly linked to MCI when TUG was performed under divided attention. Walking and turns were also most strongly associated with executive function and attention, particularly under divided attention. These differential associations with cognition were mirrored by performance costs. However, since several TUG subtasks were more strongly associated with MCI and cognitive abilities when performed under divided attention, future work is needed to determine how instrumented dual-task TUG testing can more accurately estimate risk for late-life cognitive impairment in older adults.

Introduction

The Timed Up and Go (TUG) test is widely used to assess mobility and risk of falls in older adults by geriatricians and aging researchers alike [1]. Although it was originally introduced as a test of mobility, several studies report that a longer overall TUG duration is associated with poorer cognition and faster cognitive decline in older adults [2, 3]. These findings are perhaps not surprising since voluntary actions require cognitive resources to plan, initiate, execute, and regulate the movements necessary for successful task completion [4, 5]. Nonetheless, it is not clear which components of the TUG drive its association with cognitive function and whether specific cognitive abilities are differentially related to individual TUG components.

In prior work, we quantified each of four distinct TUG subtasks (i.e., a transition from sit to stand, walking, turning, and transition from stand to sit) using a belt-worn sensor during testing in the community setting. We found that although TUG duration did not differ between those with and without mild cognitive impairment (MCI), altered postural control during the sit-to-stand transition, gait, and turns were associated with MCI status and lower cognition more generally [6]. Our other studies have shown that combinations of these TUG subtask metrics may improve the prediction of incident MCI and other adverse health outcomes [7]. However, given prior evidence that TUG components respond differently to divided attention challenges [8], dual-task performance of the TUG may uniquely affect individual subtasks, reveal how they rely on different cognitive abilities, and increase sensitivity to underlying cognitive impairment, including MCI.

In the current study, we sought to test the hypothesis that the associations between TUG subtask performances and MCI are made stronger when performed simultaneously with an unrelated task. We also hypothesized that individual subtask performances would be differentially linked to executive function and attentional abilities and affected by divided attention accordingly. To test these hypotheses, we utilized clinical, cognitive, and instrumented mobility data collected from more than 750 well-characterized dementia-free, ambulatory older adults participating in the Rush Memory and Aging Project (MAP) and Minority Aging Research Study (MARS).

Methods

Participants

Participants were drawn from two harmonized cohort studies of aging and dementia that share a common core of data collection procedures, resources, and staff at the Rush Alzheimer’s Disease Center in Chicago, IL. The Rush Memory and Aging Project (MAP), which began in 1997, is a study of older adults primarily recruited from continuous care retirement communities and subsidized housing facilities in and around the Chicago metropolitan area [9]. The Minority Aging Research Study (MARS) began in 2004 and recruits older African Americans also living within the Chicagoland area [10]. Older adults without known dementia are eligible for these studies and agree to annual clinical testing in their individual homes. Participants in MAP also agree to brain donation at autopsy at the time of death; brain donation is optional for MARS participants. Both studies were approved by the Rush Institutional Review Board and written informed consent was obtained from all participants prior to testing.

Study design

Although annual instrumented mobility testing began in 2011, dual-task Timed Up and Go (DT TUG) testing was added in 2016. The current study is a cross-sectional analysis of participants who had completed both this protocol and a cognitive assessment during the same annual testing cycle and had no presence or history of dementia at that session. At the time of analyses, 818 participants had processed DT TUG data. Of this sample, 61 were excluded for having a history of dementia (see clinical diagnosis criteria below), leaving 757 participants for study analyses (MAP, n = 531; MARS, n = 226).

Cognitive assessment

Annual cognitive testing was administered by a research assistant. Raw scores on 19 neuropsychological tests were converted to z-scores using the baseline evaluation of all participants across the parent studies. These scores were then averaged to obtain a global cognitive score, as used in prior publications [11]. To better isolate the contributions of attention and executive functioning to the global cognition summary score, we also constructed two measures from 6 of the 19 cognitive tests, as informed by prior literature (S1 Table) [12, 13]. These two metrics were compared to an episodic memory composite, which comprised 7 of the remaining tests and served as a reference domain anticipated not to have strong associations with mobility metrics.

Clinical diagnosis of MCI and dementia

Clinical diagnoses were made in a three-step process, as previously described [14]. After the cognitive tests were scored, data were then reviewed by a neuropsychologist to rate cognitive impairment in each of five domains: episodic memory, semantic memory, working memory, perceptual speed, and visuospatial ability. The presence of dementia was then determined by an experienced clinician using the guidelines of the National Institute of Neurological and Communicative Disorders and Stroke and Alzheimer’s Disease and Related Disorders Association [15]. Individuals who demonstrated evidence of cognitive impairment but not determined to have dementia were classified as having MCI, as previously described [16]. Individuals without a diagnosis of MCI or dementia were classified as having no cognitive impairment. These diagnostic determinations were used for research purposes only.

Mobility testing and recording

In-home mobility testing included two TUG trials over 8 feet (i.e., 2.4 m) for each of two conditions: with and without a concurrent requirement to perform a serial 3’s subtraction task. For the usual (normal) TUG, participants were instructed to stand up from a chair (i.e., sit-to-stand transition), walk 8 feet at their preferred pace (i.e., first 8-ft walk), return to the chair (i.e., mid-trial turn, second 8-ft walk), and sit (i.e., stand-to-sit transition). For DT TUG, participants were instructed to repeat the TUG while simultaneously subtracting threes from 100 aloud.

The testing session was recorded by a belt-worn Dynaport MoveTest (McRoberts B.V., the Netherlands) that was positioned over the lower back. This device contained a triaxial micro-electro-mechanical systems (MEMS) accelerometer and gyroscopic sensor to record acceleration and rotation, respectively, of the lower trunk at 100 Hz along each of three orthogonal directions. This state-of-the-art technology allowed us to quantify both spatiotemporal gait and trunk kinematics during the TUG procedure in the community setting. These time-stamped data were stored on onboard flash memory, then transferred to a secure RADC server for subsequent analyses.

TUG subtask sensor metrics

Each continuous TUG trial recording was used to calculate the overall duration as well as 18 quantitative metrics, according to custom-developed algorithms [17, 18]. These metrics were transformed when appropriate to reduce skewness, averaged across trials for each condition, and z-scored relative to pooled parent study performance on the normal TUG. We then used principal component analyses (PCA) to reduce these data into interpretable subtask performances, similar to our prior work [19]. Since the underlying factor structures were similar across normal and dual-task TUG, we created the same nine mobility scores for each condition, according to S2 Table.

Statistical analyses

To examine the associations of the individual TUG metrics with the odds of MCI, we first ran a series of logistic regression analyses considering overall TUG duration and each of the nine mobility scores (representing the four subtasks) as predictors of MCI for the normal and dual-task conditions separately. We then entered these measures into condition-specific forward selection stepwise procedures (p < .05 to enter, p>.1 to leave) to determine which metrics were most strongly associated with MCI at the time of mobility testing. To determine whether TUG performances were related to individual differences in cognitive abilities, we then examined linear associations with global cognition and three cognitive domains: attention, executive function, and episodic memory, and employed forward-selection linear regression models, as above. Confounding participant characteristics (i.e., age, sex, self-identified race, and years of education) were included and retained in all final models. Finally, to investigate the effects of divided attention on TUG performance (i.e., dual-task “costs”), we employed matched-pair t-tests across conditions for each of the nine mobility scores. Programming was done in SAS v.9.4 for Linux (SAS Institute Inc., Cary, NC) and R software [20]. P-values surviving Bonferroni correction (p < .0055) were considered significant.

Results

Table 1 summarizes the participant, cognitive and overall TUG performance characteristics for the 757 adults included in these analyses. Under normal and undistracted testing, a longer TUG duration was associated with higher odds of MCI (OR per SD = 1.23 [1.04, 1.46], p = .01), lower global cognitive abilities (β = -0.19, p < .001), and poorer performance across the three cognitive domains (-0.25<β<-0.09, p’s < .01). However, when TUG was performed with the serial subtraction task, overall duration was longer (Cohen’s d = .88, p < .001) and more strongly associated with MCI (OR = 1.38 [1.22, 1.56], p < .001), global cognition (β = -0.31, p < .001), and individual cognitive domains (-0.26<β<-0.22, p’s < .001).

Table 1. Participant, cognitive, and overall TUG performance characteristics.

All NCI MCI NCI vs. MCI
(n = 757) (n = 520) (n = 237) p-value
Age (years) 81±7 80±7 84±7 < .001
Female (%) 77.1 78.3 74.7 .30
Black (%) 32.9 33.6 31.5 .61
Education (years) 15.7±3.3 15.7±3.3 15.9±6.3 .57
Cognitive Performance
Mini-Mental State Exam 28.1±1.8 28.5±1.4 27.1±2.2 < .001
Global Composite (z-score) 0.24±0.27 0.43±0.46 -0.17±0.55 < .001
TUG Performance
TUG Duration (s) 15±7 14±6 17±8 < .001
 Gait speed (m/s) 0.77±0.3 0.81±0.3 0.67±0.3 < .001
DT TUG Duration (s) 21±11 19±8 26±13 < .001
 Gait speed (m/s) 0.52±0.2 0.57±0.2 0.44±0.2 < .001
DT Serial Subtraction
 Total # Responses 7.2 ± 2.4 7.33 ± 2.2 6.9 ± 2.6 .038
  # Correct 6.2 ± 2.6 6.4 ± 2.4 5.6 ± 2.7 < .001
  # Incorrect 1.0 ± 1.4 0.9 ± 1.3 1.3 ± 1.4 < .001

Associations of TUG subtasks with MCI

When we examined the relation of the nine mobility scores to MCI during the usual TUG, only slower walking pace and smaller turn magnitude were associated with higher odds of being diagnosed with MCI (Fig 1). We then considered overall task duration and all mobility scores together in a forward selection model to determine the best TUG indicators of MCI. Walking pace alone was selected by this procedure and accounted for a 2% increase in AUC beyond participant characteristics (OR = 0.71 [0.58,0.86], p < .001).

Fig 1. Quantitative TUG vs. MCI.

Fig 1

Odds ratios and 95% confidence intervals for MCI based on individual mobility performance scores during normal (light green) and dual-task (dark green) Timed Up and Go (TUG). All models were adjusted for age, sex, race (Black versus White), and education. Statistically significant associations (p < .005) do not touch the shaded box. * indicates associations that significantly differ across conditions.

For the DT TUG, 6 of 9 mobility scores were associated with higher odds of MCI (Fig 1). Walking pace was again identified as the sole predictor of MCI in forward selection procedures but was more strongly associated with MCI (OR = 0.53 [0.42, 0.66], p < .001) and accounted for a 4% increase in AUC beyond participant characteristics.

Associations of TUG subtasks with global cognition

We then examined TUG subtask performance with a continuous composite metric of global cognition. For the normal TUG, 6 of 9 mobility scores were associated with the global cognitive composite (Fig 2). Walking pace and step time variability were selected as the best TUG indicators of global cognitive abilities and accounted for 5.4% and <0.5% of the variance, respectively.

Fig 2. Quantitative TUG vs. global cognition.

Fig 2

TUG subtasks vs. the global cognition composite, adjusted for age, sex, race, and education. Nine mobility scores quantifying the four TUG subtasks were calculated for normal (light green) and dual-task (dark green) TUG. A standardized beta (β) beyond the [-0.10, 0.10] shaded box corresponds to p < .005, while a β beyond [-0.133, 0.133] corresponds to p < .0001. * indicates associations that significantly differ across conditions.

For the DT TUG, 8 of 9 mobility scores were associated with global cognition. Walking pace alone was retained after forward selection but accounted for 11.7% of the variance (as compared to 5.4% without divided attention). Fig 2 illustrates subtask associations with the global composite and their differences across conditions.

Associations of TUG subtasks with specific cognitive abilities

Next, we examined the associations of normal TUG with composites scores for executive functioning, attention, and episodic memory (Fig 3a). All 9 TUG subtask mobility scores were associated with executive functioning. Walking, turn, and stand-to-sit descent control metrics were associated with attention. Only walking pace and regularity were associated with episodic memory. In forward selection models, walking pace was the only TUG metric consistently associated with all three cognitive abilities. Pace and other metrics explained 6.7% of the variance in attention, 6% of executive functioning, and 3.6% of the episodic memory composite.

Fig 3. Quantitative TUG vs. individual cognitive domains.

Fig 3

Associations between TUG subtasks and individual cognitive abilities during (a) normal and (b) dual-task (dark green) conditions, after adjusting for age, sex, race, and education. A standardized beta (β) beyond the [-0.10, 0.10] shaded box corresponds to p < .005, while a β beyond [-0.133, 0.133] corresponds to p < .0001.

As expected, TUG associations with individual cognitive abilities were stronger with divided attention (Fig 3b) and associations with episodic memory emerged for 7 out of 9 mobility scores. Pace together with other dual-task TUG metrics explained 8% of the variance in attention, and 10.5% variance of executive function. Only 1.5% of the variation in episodic memory was explained by individual subtasks; 10% was accounted for by overall task duration. Associations with the traditional domains of our cognitive testing battery [21] may be found in S3 Table.

Effects of divided attention on TUG performance

Finally, we examined the individual dual-task costs to isolate the effect of divided attention, i.e., TUG interference by the distractor task, and account for individual differences in motor abilities. Dividing attention during the TUG was associated with a small decrease in postural complexity (Cohen’s d = -0.161, p < .001) and increase in duration (d = 0.25, p < .001) during the sit-to-stand transition, large decreases in pace (d = -1.13, p < .001), cadence (d = -1.09, p < .001), regularity (d = -0.85, p < .001), and increased step time variability (d = 0.64, p < .001) during walking. The magnitude of the turn in the middle of the trial was also substantially decreased (d = -0.82, p < .001) along with a small decrease in descent postural control (d = -0.22, p < .001) during the final stand-to-sit transition. That is, while participants tended to transition from sitting to standing more cautiously, they walked more slowly, walked and turned more irregularly, and sat more abruptly at the end of the dual-task protocol. Fig 4 illustrates the size of these effects across each of the nine mobility scores, such that the greatest effects of divided attention were observed during the walking and turning procedures and mirrored associations with global cognition. Individual quantitative metrics are also contrasted in S4 Table.

Fig 4. Dual-task cost effect sizes during the four TUG subtasks.

Fig 4

Small effects of divided attention testing (Cohen’s d<0.5; light blue) were observed in the control and duration of the sit-to-stand transition. Medium (>0.5) to large effects (>0.8; dark blue) were observed in the walking and turn procedures. A small effect was observed during the stand-to-sit transition only for postural descent control.

Discussion

We employed an unobtrusive wearable sensor to quantify TUG performance with and without divided attention in a large diverse group of dementia-free older adults within the community. We first confirmed prior work that some TUG subtasks were associated with MCI and global cognition, then observed that all TUG subtasks became more strongly linked to cognition when performed under divided attention. We further observed that the degree to which an individual subtask was associated with cognitive abilities, especially attention and executive function, mirrored the degree to which it was altered by divided attention [22]. These context-dependent performances and associations throughout the TUG warrant further investigation of how other dual-tasking paradigms might be combined with quantitative mobility assessments to unmask motor and cognitive impairments in normal-appearing older adults.

To date, the majority of studies on the cognitive correlates and consequences of divided attention on motor performance has focused on gait [23, 24]. Slower, less accurate gait performance has been linked to underlying cognition at the time of assessment [25, 26], particularly attention and executive functioning, two domains crucial for walking and any goal-directed behaviors [5]. These associations with cognitive function are then made stronger with divided attention [27]. Since greater cognitive resources are required to ensure that two different simultaneous tasks are performed correctly, gait performance may beworsened, especially when these resources are limited. As a result, physical safety is typically prioritized over other tasks, such that even self-aware adults tend to walk more slowly or stop altogether [2830] in order to keep balance and avoid harm. These same actions often foretell adverse outcomes in older age [31, 32]. Nonetheless, poorer multi-tasking abilities remain evidence of greater cognitive dysfunction.

TUG motor performances outside of gait remain largely underexplored. While task duration may be no more informative than gait speed in predicting geriatric outcomes [33], deconstructing the TUG could improve the information to be gained. Prior studies have linked compromised postural control and fluency during sit-to-stand transitions and turns with MCI and poor executive functioning [6, 34, 35]. Outside of these studies, however, we know of no publications examining instrumented TUG and cognition, especially during divided attention.

The current study suggests that the TUG may be highly informative of cognitive functioning, although clinical insight likely depends upon both subtask and context (e.g., with or without divided attention). First, we report differential associations with TUG performance and cognition across the standing, walking, turning, and sitting procedures, such that walking and turning were most strongly coupled with cognitive outcomes and walking pace (i.e., gait speed) alone best informed cognitive status and abilities. We then provide evidence that dividing attention during the TUG can leverage its inherent associations with attention and executive functioning to increase difficulty across several task performances. That is, while attentional control is necessary to focus, select, and inhibit stimuli to prioritize neural resources toward a given task, and executive functioning is necessary to maintain task set, facilitate task shifts, monitor motor-sensory input, and safely interact with environment [22], these abilities become particularly important when both are needed to perform two concomitant tasks. And, although walking was indeed the most informative subtask towards cognition, dividing attention increased both the task difficulty and dependence on higher-level resources throughout the TUG procedure. These findings suggest that dual tasking may be used to uncover even subtle links between cognition and mobility.

When investigating interference by the unrelated serial subtraction task [36], we observed dual-task costs that paralleled subtask associations with cognition and differing levels of automaticity across the TUG. To the extent that divided attention costs were present but not strongly associated with cognition (i.e., postural transitions), we postulate that some movements are confounded by acts of caution, motor impairments, or are inherently more variable within individuals (e.g., gait variability across a short distance) [2830]. That is, while costs in gait or turns offer insight towards cognitive outcomes, transitions may be better suited to predict adverse health outcomes like future frailty, falls, or disability in older adults [18].

The primary strengths of this study include our implementation of the instrumented dual-task TUG in a large, well-characterized racially diverse group of older adults in the community setting. We further contribute to existing literature by summarizing complex temporospatial gait and trunk kinematics into interpretable mobility scores via PCA, assessing cognitive-motor association effect sizes across different features of the task, and comparing these associations across conditions. To the best of our knowledge, we are also the first to observe dual-task costs that mirror associations with attentional and executive function abilities at the sub-movement level.

There are three main limitations. First, since we did not collect serial subtraction performance without TUG beyond a short practice, we were unable to assess cognitive “cost” or the relative task difficulty across normal and dual-task conditions. Second, without simultaneous recordings of verbal responses across the TUG, we were unable to ensure continuous serial subtraction task engagement or gauge task prioritization across participants. That is, since our divided attention task may not have affected all four motor subtasks to the same extent, the serial subtraction task perhaps best enhanced the cognitive correlates of ongoing motor execution, rather than earlier or later phases of the TUG. Additional testing paradigms are needed to better identify and delineate the cognitive and motor resources employed during other aspects of motor control, like movement planning, initiation, and termination. Finally, since this analysis does not consider longitudinal observations, it is not possible to infer the causal direction of the motor-cognitive associations which were observed. Further work will be needed to determine to what extent the instrumented DT TUG may improve the prediction of future cognitive impairment or other non-cognitive adverse health outcomes.

Conclusions

In conclusion, our study demonstrates that instrumented dual-task testing increases the information to be gained from the TUG. While we found walking and turning to be most strongly associated with cognitive abilities and impairment, all subtasks became more strongly linked to cognition when TUG was performed under divided attention. Motor performances were also altered by dual-tasking to the extent a subtask was associated with attention and executive function. These findings suggest dividing attention can be used to uncover both the shared and unshared resources across motor and cognitive tasks. Future work should consider similar paradigms to deconstruct complex movements, further probe the correlates of motor planning and execution, and better simulate everyday mobility and its associations with cognitive status and risk.

Supporting information

S1 Table. Attention and executive function composites.

Neuropsychological assessments used to compute composite scores of cognitive abilities across attentional and executive control domains. As in our prior publications, composite scores were constructed by averaging across centered and scaled test scores, relative to the appropriate parent study baseline.

(DOCX)

S2 Table. Mobility score components.

Measures extracted from each TUG performance were summarized as nine mobility scores to quantify four TUG subtasks. Some measures were flipped according to factor direction (e.g., AP jerk), denoted by a -1 multiplier.

(DOCX)

S3 Table. Quantitative TUG regression models for five cognitive domains.

Univariate and forward selection linear regression results for the five cognitive domains traditionally used to construct global cognition. Models feature TUG performances, adjusted for age, sex, race (Black versus White), and education. Please note that β>0.10 has significance p<0.005, while β>0.133 has significance p < .0001.

(DOCX)

S4 Table. Quantitative TUG metrics across normal and dual-task conditions.

Individual metrics used to construct the nine mobility scores, as collected during the normal and dual-task Timed Up and Go.

(DOCX)

Acknowledgments

We thank all the MAP and MARS participants, and the staff and investigators at the Rush Alzheimer’s Disease Center (RADC) for providing and processing high quality data. Please visit the RADC Research Resource Sharing Hub (www.radc.rush.edu) to obtain data for research purposes.

Data Availability

More information regarding obtaining these data for research use can be found at the RADC Research Resource Sharing Hub (www.radc.rush.edu).

Funding Statement

This study was supported by the National Institutes of Health (NIH; [grants: K01AG064044 to VNP, K25AG061254 to RJD, R01AG022018 to LLB, R01AG017917 to DAB, R01NS078009 to ASB, R01AG056352 to ASB]; the Illinois Department of Public Health to DAB; and the Robert C. Borwell Endowment Fund to DAB. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

References

  • 1.Podsiadlo D, Richardson S. The timed "Up & Go": a test of basic functional mobility for frail elderly persons. J Am Geriatr Soc. 1991;39(2):142–8. Epub 1991/02/01. doi: 10.1111/j.1532-5415.1991.tb01616.x . [DOI] [PubMed] [Google Scholar]
  • 2.Donoghue OA, Horgan NF, Savva GM, Cronin H, O’Regan C, Kenny RA. Association between timed up-and-go and memory, executive function, and processing speed. J Am Geriatr Soc. 2012;60(9):1681–6. Epub 2012/09/19. doi: 10.1111/j.1532-5415.2012.04120.x . [DOI] [PubMed] [Google Scholar]
  • 3.Beauchet O, Allali G, Montero-Odasso M, Sejdic E, Fantino B, Annweiler C. Motor phenotype of decline in cognitive performance among community-dwellers without dementia: population-based study and meta-analysis. PLoS One. 2014;9(6):e99318. Epub 2014/06/10. doi: 10.1371/journal.pone.0099318 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Woollacott M, Shumway-Cook A. Attention and the control of posture and gait: a review of an emerging area of research. Gait Posture. 2002;16(1):1–14. doi: 10.1016/s0966-6362(01)00156-4 . [DOI] [PubMed] [Google Scholar]
  • 5.Yogev-Seligmann G, Hausdorff JM, Giladi N. The role of executive function and attention in gait. Movement Disorders. 2008;23(3):329–42- quiz 472. doi: 10.1002/mds.21720 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Mirelman A, Weiss A, Buchman AS, Bennett DA, Giladi N, Hausdorff JM. Association between performance on Timed Up and Go subtasks and mild cognitive impairment: further insights into the links between cognitive and motor function. J Am Geriatr Soc. 2014;62(4):673–8. Epub 2014/03/17. doi: 10.1111/jgs.12734 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Buchman AS, Dawe RJ, Leurgans SE, Curran TA, Truty T, Yu L, et al. Different Combinations of Mobility Metrics Derived From a Wearable Sensor Are Associated With Distinct Health Outcomes in Older Adults. J Gerontol A Biol Sci Med Sci. 2020;75(6):1176–83. Epub 2019/06/28. doi: 10.1093/gerona/glz160 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Coulthard JT, Treen TT, Oates AR, Lanovaz JL. Evaluation of an inertial sensor system for analysis of timed-up-and-go under dual-task demands. Gait Posture. 2015;41(4):882–7. Epub 20150321. doi: 10.1016/j.gaitpost.2015.03.009 . [DOI] [PubMed] [Google Scholar]
  • 9.Bennett DA, Buchman AS, Boyle PA, Barnes LL, Wilson RS, Schneider JA. Religious Orders Study and Rush Memory and Aging Project. J Alzheimers Dis. 2018;64(s1):S161–S89. doi: 10.3233/JAD-179939 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Barnes LL, Shah RC, Aggarwal NT, Bennett DA, Schneider JA. The Minority Aging Research Study: ongoing efforts to obtain brain donation in African Americans without dementia. Curr Alzheimer Res. 2012;9(6):734–45. doi: 10.2174/156720512801322627 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Wilson RS, Boyle PA, Yu L, Barnes LL, Sytsma J, Buchman AS, et al. Temporal course and pathologic basis of unawareness of memory loss in dementia. Neurology. 2015;85(11):984–91. Epub 20150826. doi: 10.1212/WNL.0000000000001935 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Riley E, Mitko A, Stumps A, Robinson M, Milberg W, McGlinchey R, et al. Clinically significant cognitive dysfunction in OEF/OIF/OND veterans: Prevalence and clinical associations. Neuropsychology. 2019;33(4):534–46. Epub 20190404. doi: 10.1037/neu0000529 . [DOI] [PubMed] [Google Scholar]
  • 13.Esterman M, Stumps A, Jagger-Rickels A, Rothlein D, DeGutis J, Fortenbaugh F, et al. Evaluating the evidence for a neuroimaging subtype of posttraumatic stress disorder. Sci Transl Med. 2020;12(568). doi: 10.1126/scitranslmed.aaz9343 . [DOI] [PubMed] [Google Scholar]
  • 14.Bennett DA, Schneider JA, Buchman AS, Mendes de Leon C, Bienias JL, Wilson RS. The Rush Memory and Aging Project: study design and baseline characteristics of the study cohort. Neuroepidemiology. 2005;25(4):163–75. Epub 2005/08/15. doi: 10.1159/000087446 . [DOI] [PubMed] [Google Scholar]
  • 15.McKhann G, Drachman D, Folstein M, Katzman R, Price D, Stadlan EM. Clinical diagnosis of Alzheimer’s disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer’s Disease. Neurology. 1984;34(7):939–44. Epub 1984/07/01. doi: 10.1212/wnl.34.7.939 . [DOI] [PubMed] [Google Scholar]
  • 16.Bennett DA, Wilson RS, Schneider JA, Evans DA, Beckett LA, Aggarwal NT, et al. Natural history of mild cognitive impairment in older persons. Neurology. 2002;59(2):198–205. doi: 10.1212/wnl.59.2.198 . [DOI] [PubMed] [Google Scholar]
  • 17.Weiss A, Herman T, Plotnik M, Brozgol M, Maidan I, Giladi N, et al. Can an accelerometer enhance the utility of the Timed Up & Go Test when evaluating patients with Parkinson’s disease? Med Eng Phys. 2010;32(2):119–25. Epub 2009/11/25. doi: 10.1016/j.medengphy.2009.10.015 . [DOI] [PubMed] [Google Scholar]
  • 18.Weiss A, Herman T, Plotnik M, Brozgol M, Giladi N, Hausdorff JM. An instrumented timed up and go: the added value of an accelerometer for identifying fall risk in idiopathic fallers. Physiol Meas. 2011;32(12):2003–18. Epub 2011/11/17. doi: 10.1088/0967-3334/32/12/009 . [DOI] [PubMed] [Google Scholar]
  • 19.Buchman AS, Leurgans SE, Weiss A, Vanderhorst V, Mirelman A, Dawe R, et al. Associations between quantitative mobility measures derived from components of conventional mobility testing and Parkinsonian gait in older adults. PLoS One. 2014;9(1):e86262. Epub 2014/01/22. doi: 10.1371/journal.pone.0086262 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Team RC, others. R: A language and environment for statistical computing. 2018.
  • 21.Bennett DA, Schneider JA, Buchman AS, Barnes LL, Boyle PA, Wilson RS. Overview and findings from the rush Memory and Aging Project. Curr Alzheimer Res. 2012;9(6):646–63. doi: 10.2174/156720512801322663 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Bayot M, Dujardin K, Tard C, Defebvre L, Bonnet CT, Allart E, et al. The interaction between cognition and motor control: A theoretical framework for dual-task interference effects on posture, gait initiation, gait and turning. Neurophysiol Clin. 2018;48(6):361–75. Epub 2018/11/30. doi: 10.1016/j.neucli.2018.10.003 . [DOI] [PubMed] [Google Scholar]
  • 23.Smith E, Cusack T, Blake C. The effect of a dual task on gait speed in community dwelling older adults: A systematic review and meta-analysis. Gait Posture. 2016;44:250–8. Epub 2015/12/21. doi: 10.1016/j.gaitpost.2015.12.017 . [DOI] [PubMed] [Google Scholar]
  • 24.Smith E, Walsh L, Doyle J, Greene B, Blake C. Effect of a dual task on quantitative Timed Up and Go performance in community-dwelling older adults: A preliminary study. Geriatr Gerontol Int. 2017;17(8):1176–82. Epub 2016/07/18. doi: 10.1111/ggi.12845 . [DOI] [PubMed] [Google Scholar]
  • 25.Morris R, Lord S, Bunce J, Burn D, Rochester L. Gait and cognition: Mapping the global and discrete relationships in ageing and neurodegenerative disease. Neurosci Biobehav Rev. 2016;64:326–45. Epub 20160223. doi: 10.1016/j.neubiorev.2016.02.012 . [DOI] [PubMed] [Google Scholar]
  • 26.Park H, Aul C, DeGutis J, Lo OY, Poole VN, McGlinchey R, et al. Evidence for a Specific Association Between Sustained Attention and Gait Speed in Middle-to-Older-Aged Adults. Front Aging Neurosci. 2021;13:703434. Epub 20210705. doi: 10.3389/fnagi.2021.703434 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Muir SW, Speechley M, Wells J, Borrie M, Gopaul K, Montero-Odasso M. Gait assessment in mild cognitive impairment and Alzheimer’s disease: the effect of dual-task challenges across the cognitive spectrum. Gait Posture. 2012;35(1):96–100. Epub 20110922. doi: 10.1016/j.gaitpost.2011.08.014 . [DOI] [PubMed] [Google Scholar]
  • 28.Neider MB, Gaspar JG, McCarley JS, Crowell JA, Kaczmarski H, Kramer AF. Walking and talking: dual-task effects on street crossing behavior in older adults. Psychology and aging. 2011;26(2):260. doi: 10.1037/a0021566 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Yogev-Seligmann G, Rotem-Galili Y, Mirelman A, Dickstein R, Giladi N, Hausdorff JM. How Does Explicit Prioritization Alter Walking During Dual-Task Performance? Effects of Age and Sex on Gait Speed and Variability. Physical Therapy. 2010;90(2):177–86. doi: 10.2522/ptj.20090043 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Lundin-Olsson L, Nyberg L, Gustafson Y. "Stops walking when talking" as a predictor of falls in elderly people. Lancet. 1997;349(9052):617. doi: 10.1016/S0140-6736(97)24009-2 . [DOI] [PubMed] [Google Scholar]
  • 31.Maki BE. Gait changes in older adults: predictors of falls or indicators of fear. J Am Geriatr Soc. 1997;45(3):313–20. doi: 10.1111/j.1532-5415.1997.tb00946.x . [DOI] [PubMed] [Google Scholar]
  • 32.Bueno GAS, Gervásio FM, Ribeiro DM, Martins AC, Lemos TV, de Menezes RL. Fear of Falling Contributing to Cautious Gait Pattern in Women Exposed to a Fictional Disturbing Factor: A Non-randomized Clinical Trial. Front Neurol. 2019;10:283. Epub 2019/03/26. doi: 10.3389/fneur.2019.00283 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Viccaro LJ, Perera S, Studenski SA. Is timed up and go better than gait speed in predicting health, function, and falls in older adults? J Am Geriatr Soc. 2011;59(5):887–92. Epub 20110315. doi: 10.1111/j.1532-5415.2011.03336.x . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Ansai JH, Andrade LP, Nakagawa TH, Vale FAC, Caetano MJD, Lord SR, et al. Cognitive Correlates of Timed Up and Go Subtasks in Older People With Preserved Cognition, Mild Cognitive Impairment, and Alzheimer’s Disease. Am J Phys Med Rehabil. 2017;96(10):700–5. Epub 2017/02/09. doi: 10.1097/PHM.0000000000000722 . [DOI] [PubMed] [Google Scholar]
  • 35.Sunderaraman P, Maidan I, Kozlovski T, Apa Z, Mirelman A, Hausdorff JM, et al. Differential Associations Between Distinct Components of Cognitive Function and Mobility: Implications for Understanding Aging, Turning and Dual-Task Walking. Front Aging Neurosci. 2019;11:166. Epub 2019/07/18. doi: 10.3389/fnagi.2019.00166 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Coppin AK, Shumway-Cook A, Saczynski JS, Patel KV, Ble A, Ferrucci L, et al. Association of executive function and performance of dual-task physical tests among older adults: analyses from the InChianti study. Age and Ageing. 2006;35(6):619–24. doi: 10.1093/ageing/afl107 [DOI] [PMC free article] [PubMed] [Google Scholar]

Decision Letter 0

Eric R Anson

9 Mar 2022

PONE-D-21-36468Dividing attention during the Timed Up and Go enhances associations of subtask performances with MCI and cognitionPLOS ONE

Dear Dr. Poole,

Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process.

As you can see from the reviewers responses, there is substantial enthusiasm for this manuscript.  There are however several areas that will benefit from additional clarification.  It is important that the authors address the concerns of the reviewer with respect to state of the art versus novelty, keeping in mind that novelty is not a requirement for publication in PLOS ONE.  Adding this information to the manuscript will better place this manuscript within the existing body of literature.

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Comments to the Author

1. Is the manuscript technically sound, and do the data support the conclusions?

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Reviewer #1: Yes

Reviewer #2: Partly

**********

2. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: I Don't Know

Reviewer #2: Yes

**********

3. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #2: No

**********

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Reviewer #1: Yes

Reviewer #2: Yes

**********

5. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: Dear Authors:

This is a very interesting study very pleasant to read and within a very pertinent and current area of interest.

The main strengths of this study is the implementation of the instrumented TUG with and without divided attention and thorough cognitive assessment in a large, well-characterized racially diverse group of older adults.

In my opinion the main limitations were also conveniently addressed.

Leave only the suggestion to consider the inclusion of a last subsection referring to the main conclusions of this study.

Reviewer #2: The paper is interesting and well written. The methodology is clear, and the analysis conducted thoroughly. However, I found some tricky points that, in my opinion, need clarification. Below I list the correction, doubts, and suggestions I have. I will divide them into general and specific arguments.

General comments:

1) as aforementioned said, the paper is clear and rigorous. Still, I have some concerns about the novelty. I would ask the authors to highlight the novelty of the work (if any) in terms of protocol, experimental design, kinematics/statistical analysis, or results. It is not clear what is scientific advancement compared to the state of the art.

2) State of art and related works are not sufficiently addressed.

3) It seems that the majority part of the paper results refers to the TUG walking subtask. Therefore, I wonder why the authors adopted the TUG as the motor activity rather than the commonly used walk task?

Specific Comments:

1) line 130, paragraph "Clinical Diagnosis of MCI and dementia": it is not clear if the test used served for the clinical diagnosis, research purposes, or both.

2) line 151, paragraph “Mobility Testing and Recording”: referring the sentence "…contained a tri-axial accelerometer and three gyroscopes..." is it possible that the authors meant a three-axis gyroscope instead of three gyroscopes?

3) lines 155-161, paragraph "TUG subtask sensor metrics": I found this part a bit convoluted. I would suggest the authors to make it clearer.

4) line 163, paragraph "TUG subtask sensor metrics": referring to the sentence "…by calculating the motor "cost..."" it seems that the scientific literature refers to this concept as “Dual-Task Cost (DTC)”. If it is so, I would suggest the authors to comply with this.

5) line 183, paragraph "Result": I would recommend the author to report the result consistently: e.g. line 190, there is no p-value associated to beta intervals. Check the section and homogenize the way you present the results, please.

6) line 249 section "Association of TUG subtasks with global cognition": I am wondering if beta levels should not be reported as an absolute value.

**********

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Reviewer #1: No

Reviewer #2: No

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PLoS One. 2022 Aug 3;17(8):e0269398. doi: 10.1371/journal.pone.0269398.r002

Author response to Decision Letter 0


27 Apr 2022

We would like to thank the editor and reviewers for the thoughtful critique of our manuscript and opportunity to submit a revision to PLOS ONE. We believe the manuscript is markedly improved after adding a concluding paragraph that highlights our study’s takeaways (Reviewer 1), and better clarifying its approach, novelty, and context within the existing literature (Reviewer 2). We have also reformatted the manuscript, in accordance with the PLOS requirements. Our specific responses to each review are emphasized below.

Response to Reviewers

1. Please ensure that your manuscript meets PLOS ONE's style requirements, including those for file naming. The PLOS ONE style templates can be found at

https://journals.plos.org/plosone/s/file?id=wjVg/PLOSOne_formatting_sample_main_body.pdf

and

https://journals.plos.org/plosone/s/file?id=ba62/PLOSOne_formatting_sample_title_authors_affiliations.pdf

>> Thank you for sharing. We believe the manuscript now meets PLOS ONE’s style requirements.

Reviewer #1: Dear Authors:

This is a very interesting study very pleasant to read and within a very pertinent and current area of interest.

The main strengths of this study include the implementation of the instrumented TUG with and without divided attention and thorough cognitive assessment in a large, well-characterized racially diverse group of older adults.

In my opinion the main limitations were also conveniently addressed.

Leave only the suggestion to consider the inclusion of a last subsection referring to the main conclusions of this study.

>> Thank you for the kind feedback. We now include a final paragraph that summarizes our main conclusions.

Lines 389-398 now read:

“In conclusion, our study demonstrates that instrumented dual-task testing increases the information to be gained from the TUG. While we found walking and turning to be most strongly associated with cognitive abilities and impairment, all subtasks became more strongly linked to cognition when TUG was performed under divided attention. Motor performances were also altered by dual-tasking to the extent a subtask was associated with attention and executive function. These findings suggest dividing attention can be used to uncover both the shared and unshared resources across motor and cognitive tasks. Future work should consider similar paradigms to deconstruct complex movements, further probe the correlates of motor planning and execution, and better simulate everyday mobility and its associations with cognitive status and risk.”

Reviewer #2: The paper is interesting and well written. The methodology is clear, and the analysis conducted thoroughly. However, I found some tricky points that, in my opinion, need clarification. Below I list the correction, doubts, and suggestions I have. I will divide them into general and specific arguments.

>> Thank you for the careful review and suggestions.

General comments:

1) as aforementioned said, the paper is clear and rigorous. Still, I have some concerns about the novelty. I would ask the authors to highlight the novelty of the work (if any) in terms of protocol, experimental design, kinematics/statistical analysis, or results. It is not clear what is scientific advancement compared to the state of the art.

>> Thank you. We believe this work is novel for several reasons.

First, whereas very few studies have been able to deconstruct the TUG into its individual subtasks, we have deployed a wearable device able to quantify its spatiotemporal gait and postural movements in a large number of well-characterized older adults outside of clinic and lab, in the community setting. We further summarized these complex movements into interpretable mobility scores via PCA and report novel cognitive-motor associations across subtasks and conditions. Finally, to the best of our knowledge, we are the first to observe dual-task costs that mirrored associations with attentional and executive function abilities at the sub-movement level.

These contributions are now listed as study strengths on Lines 364-371.

2) State of art and related works are not sufficiently addressed.

>> Thank you. We now emphasize our combined use of the state-of-the-art McRoberts’ Dynaport MoveTest device with subsequent principal component analyses as critical to summarize the complex TUG into interpretable motor performances.

Lines 160-161: “This state-of-the-art technology allowed us to quantify both spatiotemporal gait and trunk kinematics during the TUG procedure in the community setting.”

Lines 169-171: “We then used principal component analyses (PCA) to reduce these [18 quantitative measures] into interpretable subtask performances, similar to our prior work.”

3) It seems that the majority part of the paper results refers to the TUG walking subtask. Therefore, I wonder why the authors adopted the TUG as the motor activity rather than the commonly used walk task?

>> Thank you for this question. By focusing on the TUG task, we were able to build upon our prior work and test the hypothesis that dual-tasking would enhance our ability to detect MCI from various movements throughout the TUG procedure. We were also able to determine the extent to which the individual subtasks depended on higher-level cognitive resources. Although walking was indeed the most informative subtask towards cognition, we believe it also noteworthy that even relatively automated sub-movements (i.e., transitions) were more closely coupled with cognition when performed under divided attention. These findings suggest that dual tasking may also be used to uncover otherwise subtle links between cognition and mobility (Lines 340-353).

Specific Comments:

1) line 130, paragraph "Clinical Diagnosis of MCI and dementia": it is not clear if the test used served for the clinical diagnosis, research purposes, or both.

>> Line 144 now states: “These diagnostic determinations were used for research purposes only.”

2) line 151, paragraph “Mobility Testing and Recording”: referring the sentence "…contained a tri-axial accelerometer and three gyroscopes..." is it possible that the authors meant a three-axis gyroscope instead of three gyroscopes?

>> Thank you for this question. The reviewer is correct.

Lines 157-159 now read: “This device contained a triaxial micro-electro-mechanical systems (MEMS) accelerometer and gyroscopic sensor to record acceleration and rotation, respectively, of the lower trunk at 100 Hz along each of three orthogonal directions.”

3) lines 155-161, paragraph "TUG subtask sensor metrics": I found this part a bit convoluted. I would suggest the authors to make it clearer.

>> Thank you for this suggestion.

Lines 166-173 now read: “Each continuous TUG trial recording was used to calculate the overall duration as well as 18 quantitative metrics, according to custom-developed algorithms. These metrics were transformed when appropriate to reduce skewness, averaged across trials for each condition, and z-scored relative to pooled parent study performance on the normal TUG. We then used principal component analyses (PCA) to reduce these data into interpretable subtask performances, similar to our prior work. Since the underlying factor structures were similar across normal and dual-task TUG, we created the same nine mobility scores for each condition, according to S2 Table.”

We have also tried to improve the clarity and flow throughout the manuscript.

4) line 163, paragraph "TUG subtask sensor metrics": referring to the sentence "…by calculating the motor "cost..."" it seems that the scientific literature refers to this concept as “Dual-Task Cost (DTC)”. If it is so, I would suggest the authors to comply with this.

>> Thank you. We now explicitly refer to motor costs as “dual-task costs” to better complement the literature.

5) line 183, paragraph "Result": I would recommend the author to report the result consistently: e.g. line 190, there is no p-value associated to beta intervals. Check the section and homogenize the way you present the results, please.

>> Thank you. All p-values are now reported.

6) line 249 section "Association of TUG subtasks with global cognition": I am wondering if beta levels should not be reported as an absolute value.

>> Thank you, we now include ranges (e.g., [-.10, .10]) to better highlight the different directions of association.

Attachment

Submitted filename: Response to Reviewers.pdf

Decision Letter 1

Eric R Anson

20 May 2022

Dividing attention during the Timed Up and Go enhances associations of several subtask performances with MCI and cognition

PONE-D-21-36468R1

Dear Dr. Poole,

We’re pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it meets all outstanding technical requirements.

Within one week, you’ll receive an e-mail detailing the required amendments. When these have been addressed, you’ll receive a formal acceptance letter and your manuscript will be scheduled for publication.

An invoice for payment will follow shortly after the formal acceptance. To ensure an efficient process, please log into Editorial Manager at http://www.editorialmanager.com/pone/, click the 'Update My Information' link at the top of the page, and double check that your user information is up-to-date. If you have any billing related questions, please contact our Author Billing department directly at authorbilling@plos.org.

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Kind regards,

Eric R. Anson

Academic Editor

PLOS ONE

Additional Editor Comments (optional):

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation.

Reviewer #1: All comments have been addressed

**********

2. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Yes

**********

3. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: Yes

**********

4. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

**********

5. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

**********

6. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: (No Response)

**********

7. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: Yes: Catarina Godinho

Acceptance letter

Eric R Anson

26 Jul 2022

PONE-D-21-36468R1

Dividing attention during the Timed Up and Go enhances associations of several subtask performances with MCI and cognition

Dear Dr. Poole:

I'm pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now with our production department.

If your institution or institutions have a press office, please let them know about your upcoming paper now to help maximize its impact. If they'll be preparing press materials, please inform our press team within the next 48 hours. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information please contact onepress@plos.org.

If we can help with anything else, please email us at plosone@plos.org.

Thank you for submitting your work to PLOS ONE and supporting open access.

Kind regards,

PLOS ONE Editorial Office Staff

on behalf of

Dr. Eric R. Anson

Academic Editor

PLOS ONE

Associated Data

    This section collects any data citations, data availability statements, or supplementary materials included in this article.

    Supplementary Materials

    S1 Table. Attention and executive function composites.

    Neuropsychological assessments used to compute composite scores of cognitive abilities across attentional and executive control domains. As in our prior publications, composite scores were constructed by averaging across centered and scaled test scores, relative to the appropriate parent study baseline.

    (DOCX)

    S2 Table. Mobility score components.

    Measures extracted from each TUG performance were summarized as nine mobility scores to quantify four TUG subtasks. Some measures were flipped according to factor direction (e.g., AP jerk), denoted by a -1 multiplier.

    (DOCX)

    S3 Table. Quantitative TUG regression models for five cognitive domains.

    Univariate and forward selection linear regression results for the five cognitive domains traditionally used to construct global cognition. Models feature TUG performances, adjusted for age, sex, race (Black versus White), and education. Please note that β>0.10 has significance p<0.005, while β>0.133 has significance p < .0001.

    (DOCX)

    S4 Table. Quantitative TUG metrics across normal and dual-task conditions.

    Individual metrics used to construct the nine mobility scores, as collected during the normal and dual-task Timed Up and Go.

    (DOCX)

    Attachment

    Submitted filename: Response to Reviewers.pdf

    Data Availability Statement

    More information regarding obtaining these data for research use can be found at the RADC Research Resource Sharing Hub (www.radc.rush.edu).


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