ORIGINAL RESEARCH article

Front. Aging Neurosci., 12 August 2026

Sec. Parkinson’s Disease and Aging-related Movement Disorders

Volume 18 - 2026 | https://doi.org/10.3389/fnagi.2026.1896308

Dual-task gait and gait-cognition coupling in patients with Parkinson’s disease versus healthy older adults: moderation by cognitive status

  • Department of Neurology, College of Medicine, Dong-A University, Busan, Republic of Korea

Abstract

Background:

Gait impairment and cognitive decline frequently co-occur in Parkinson’s disease (PD), yet how cognitive status modulates dual-task gait-cognition relationships remains poorly characterized.

Objective:

To compare spatiotemporal gait parameters and dual-task costs (DTCs) between drug-naïve PD and healthy older adults (HO), and to examine how cognitive status modulates gait-cognition associations within PD.

Methods:

One hundred twenty-four participants (65 PD, 59 HO) were prospectively enrolled. PD patients were subclassified into cognitively normal (PDCN, n = 38) and mild cognitive impairment (PDMCI, n = 27) groups. Gait was assessed using the GAITRite system under four conditions: preferred speed, serial sevens subtraction, cell phone use, and backward walking. Partial Spearman correlations and moderation analyses were conducted.

Results:

PD-related gait impairments were more pronounced under dual-task conditions, with cell phone use yielding the greatest between-group differences in spatiotemporal parameters and DTCs. Gait-cognition associations in the total PD group were most consistently observed during cell phone use, involving executive, language, and attention domains. DTCs were specifically correlated with executive and language domains. Subgroup analyses revealed distinct cognitive-motor profiles: PDCN showed a paradoxical pattern in which better visuospatial function was associated with greater gait variability, while PDMCI exhibited broader positive correlations between multiple cognitive domains and gait stability. Moderation analyses confirmed these patterns were statistically distinct.

Conclusion:

Dual-task gait assessment using a cell phone paradigm may effectively characterizes cognitive-motor decline in early drug-naïve PD. Cognitive status qualitatively modulates gait-cognition coupling, with domain-specific patterns differing between PDCN and PDMCI, with implications for targeted monitoring and intervention.

Introduction

Gait is no longer viewed as a purely autonomous motor activity (Yogev-Seligmann et al., 2008). Instead, it is recognized as a complex activity integrated with higher-order cognitive domains, such as executive function, attention, and processing of internal and external stimuli (Amboni et al., 2013). Accordingly, specific gait disturbances have emerged as potential indicators of cognitive deterioration (Verghese et al., 2008). This is particularly relevant in Parkinson’s disease (PD), a neurodegenerative condition wherein both gait and cognition are prominently affected. Gait impairments in PD have been shown to vary according to cognitive subgroup, and patients with mild cognitive impairment (PDMCI) show poorer performance than those with normal cognition (PDCN), a disparity that has been shown to be especially evident under more cognitively demanding conditions (Amboni et al., 2022). Among PDMCI subtypes, multiple-domain and amnestic subtypes have been associated with worse gait patterns, particularly when an additional cognitive load is imposed. Non-amnestic multiple-domain PDMCI is linked to pronounced postural instability and gait disturbances, indicating that the breadth of cognitive involvement may be a key driver of motor deterioration (Goldman et al., 2012).

Beyond its relationship with cognition, gait impairment in PD is among the most common and disabling symptoms, worsening as the disease progresses (Zhang et al., 2024), and has been closely linked to reduced quality of life, increased mortality, and fall risk (Amara et al., 2025; Gonzalez et al., 2022). Furthermore, because walking in daily life frequently involves concurrent activities, dual-task walking has gained considerable attention as a clinically relevant assessment tool. This focus has led to the widespread use of dual-task cost (DTC) metrics (Monaghan et al., 2023). The DTC quantifies the relative change in performance during dual-task gait in comparison with single-task gait, providing valuable insights into the extent of gait deterioration resulting from added cognitive or motor loads. The interaction between gait and cognition is fundamentally based on the concept of limited resource-capacity sharing (Tombu and Jolicoeur, 2003). When a cognitive or motor load is added, the brain must allocate limited neural resources between the two tasks, often leading to cognitive–motor interference, wherein individuals must employ strategies such as task prioritization or compensation to manage the competing demands (Johansson et al., 2021). Prior studies have examined dual-task gait parameters across cognitive subgroups within PD. Di Filippo et al. (2025) demonstrated that dual-task-related gait alterations follow a gradient corresponding to the degree of cognitive dysfunction, becoming progressively more pronounced from PD with normal cognition (PD-noCI) through subjective cognitive impairment (PD-SCI) to MCI (PD-MCI), suggesting that even subclinical cognitive decline may be detectable via dual-task gait. In contrast, a systematic review and meta-analysis by Msigwa et al. (2026) reported that while dual-task gait parameters reliably distinguished PD with cognitive impairment from cognitively normal PD, no significant differences were observed between PD-SCI and PD-noCI, highlighting an unresolved discrepancy regarding the sensitivity of dual-task gait at the earliest stages of cognitive decline. Importantly, both studies lacked a healthy control group, limiting their ability to disentangle disease-specific gait alterations from those attributable to normative aging. Moreover, participants were predominantly levodopa-treated patients across variable disease stages, introducing heterogeneity in baseline gait that complicates interpretation of dual-task effects. Critically, neither study employed dual-task cost (DTC) metrics, which normalize for individual differences in baseline gait performance and thereby provide a more sensitive index of cognitive-motor interference. Furthermore, prior studies have predominantly employed a single cognitive dual-task paradigm, typically serial subtraction or auditory stroop tasks, which may not adequately capture the complexity of real-world cognitive-motor demands. These limitations underscore the need for studies conducted in early-stage, drug-naïve PD cohorts that include a healthy control group, employ DTC as a primary outcome measure, and incorporate ecologically valid dual-task paradigms to better characterize cognitive-motor interactions in PD.

Therefore, the purpose of this study was to compare spatiotemporal gait parameters and DTCs between individuals with PD and HO under single- and dual-task walking conditions, incorporating multiple task conditions of varying ecological validity, with a particular focus on a cell phone use task as an ecologically valid cognitive-motor dual-task reflecting a ubiquitous real-world activity. In addition, we examined the associations between spatiotemporal gait parameters and specific cognitive domains in each group. As a secondary aim, we explored whether these gait–cognition associations differed further in relation to the cognition status within the PD group, comparing patients with PDCN and those with PDMCI. Through this multilevel analytical approach, this study sought to identify the gait metrics and task conditions that were most sensitive to cognitive status and to elucidate the cognitive–motor mechanisms that underlie gait deterioration in PD.

Methods

Study population

The participants were prospectively recruited from a tertiary referral hospital between July 2023 and February 2025. The study cohort consisted of HO and patients diagnosed with PD. All patients fulfilled the Movement Disorder Society (MDS) clinical diagnostic criteria for PD and were drug-naïve at the time of the assessment (Postuma et al., 2015). The HO group consisted of caregivers of patients with Parkinsonian disorders and community-dwelling volunteers. For both groups, inclusion was restricted to individuals aged 60–80 years who were independently ambulatory and showed no functional limitations in daily living. Participants in the HO group were required to have no history of neurological deficits or cognitive impairment. All participants underwent global cognitive screening; in addition, patients with PD completed a comprehensive neuropsychological battery. On the basis of the results of this battery, patients with PD were categorized into PDCN and PDMCI in accordance with published diagnostic criteria (Litvan et al., 2012). The exclusion criteria for both groups were as follows: (1) medical or musculoskeletal conditions that could significantly interfere with gait performance; (2) co-existing neurological disorders other than PD; and (3) a history of major psychiatric illness.

Neuropsychological assessment

All participants underwent global cognitive screening using the Korean version of the Montreal Cognitive Assessment (K-MoCA) (Kang et al., 2009). For the K-MoCA, domain-specific subscores were derived in accordance with a previously proposed categorization (Miyamoto and Miyamoto, 2022), which encompassed visuospatial/executive function, attention, language, memory, and orientation. In addition, all patients with PD underwent a comprehensive neuropsychological battery to evaluate five distinct cognitive domains: (1) attention (Digit Span Forward/Backward and Color Word Stroop Test); (2) language (Boston Naming Test); (3) visuospatial function (Rey-Osterrieth Complex Figure Test copy); (4) memory (Seoul Verbal Learning Test and Rey-Osterrieth Complex Figure Test); and (5) executive function (Controlled Oral Word Association Test) (Yoo et al., 2021). For each test, raw scores were converted into standardized Z-scores based on age-, sex-, and education-adjusted normative data. Domain composite scores were calculated by averaging the Z-scores of the individual tests within each domain.

Gait assessment protocol

Gait performance was assessed using the GAITRite Electronic Walkway system (CIR Systems Inc., Peekskill, NY, USA), which consists of a 6-m-long and 0.6-m-wide pressure-sensitive mat embedded with sensors to capture spatiotemporal gait parameters with high resolution. The participants completed all the assessments barefoot. Height, weight, and mean leg length (defined as the distance from the medial malleolus to the anterior inferior iliac spine) were measured before evaluation. Each participant completed the walking trials under the following four conditions: (1) preferred speed, (2) serial sevens subtraction (cognitive dual-task), (3) cell phone use, in which participants typed a pre-specified, randomly ordered numeric sequence using the default numeric keypad on a smartphone while walking (cognitive–motor dual-task), and (4) backward walking (motor-challenging task requiring altered locomotor control). The mean values of the spatiotemporal gait parameters across three trials were used for the analysis. All assessments were conducted in a quiet, well-lit environment, and participants were given standardized instructions prior to each condition to ensure consistency across trials.

The mean values of 16 spatiotemporal gait parameters were collected and categorized into five domains: pace, variability, rhythm, asymmetry, and postural control (Galna et al., 2015). The pace domain included stride velocity (cm/s), step length (cm), and swing time standard deviation (SD) (s). The variability domain consisted of the step time SD (s), stance time SD (s), stride velocity SD (cm/s), and step length SD (cm). The rhythm domain consisted of step time (s), swing time (s), and stance time (s). The asymmetry domain included step-time asymmetry (s), swing-time asymmetry (s), and stance-time asymmetry (s). The postural control domain consisted of step-length asymmetry (cm), base of support (cm), and base of support SD (cm).

DTC was computed for the dual-task conditions (serial sevens subtraction and cell phone use), and an equivalent relative gait cost was calculated for backward walking, using the following formula:

The resulting values were labeled according to the corresponding condition: %Δ2–1 for serial sevens subtraction (cognitive dual-task cost), %Δ3–1 for cell phone use (cognitive–motor dual-task cost), and %Δ4–1 for backward walking (motor-challenge cost), each referenced to the preferred speed condition. The DTC parameter reflected how the additional cognitive and motor loads introduced during the dual-task conditions affected gait performance, thereby integrating both gait and cognitive–motor assessments (Ali et al., 2025). For backward walking, %Δ4–1 is interpreted as the relative gait-performance cost under a motor-challenging condition rather than as evidence of cognitive–motor dual-task interference.

Ethics approval statement

The protocol of this study was approved by the Ethics Committee of the Dong-A University Hospital. Written informed consent was obtained from all participants. All processes of this study were carried out in accordance with the Declaration of Helsinki.

Statistical analyses

Continuous variables are presented as mean ± SD, while categorical variables were reported as frequencies. Normality was assessed using the Shapiro–Wilk test. For demographic and clinical characteristics, differences between the HO and total PD groups were examined using the Mann–Whitney U test, chi-square test, or independent t-test, as appropriate. For variables requiring covariate adjustment, a ranked analysis of covariance (ANCOVA) was performed, controlling for age, sex, and educational attainment. For comparisons among the three subgroups (HO, PDCN, and PDMCI), the Kruskal–Wallis test, chi-square test, one-way analysis of variance (ANOVA), or ranked ANCOVA with the same covariates was employed as appropriate. For the primary analysis of spatiotemporal gait parameters and DTC, group differences were evaluated using ranked ANCOVA adjusted for age, sex, mean leg length, and educational attainment. The gait profiles were visualized as Z-scores based on the mean and SD of the HO group.

Partial Spearman’s correlation analyses were conducted to examine the relationships between gait and cognition across different levels of comparison. Within the total PD group, correlations were obtained between gait parameters and neuropsychological domain composite scores; this analysis was restricted to parameters that demonstrated significant differences in the primary PD versus HO comparisons, with false discovery rate (FDR) correction applied separately within each task condition. To further explore gait–cognition associations, correlations were also obtained between spatiotemporal gait parameters and total scores and domain-specific subscores of the K-MoCA within each group (PD and HO separately); this analysis was restricted to parameters showing significant PD versus HO group differences, where applicable. As an exploratory subgroup analysis, correlations were also obtained between the spatiotemporal gait parameters and neuropsychological domain composite scores within the PDCN and PDMCI groups separately, restricted to parameters showing significant differences between these two subgroups. For the latter two analyses, nominal p-values are reported given their exploratory nature. All the models were adjusted for age, sex, and mean leg length. Although the neuropsychological domain composite scores were derived from age-, sex-, and education-referenced normative data, these covariates were retained to ensure appropriate adjustment of spatiotemporal gait parameters. To formally evaluate whether cognitive status moderated the gait–cognition associations identified in the subgroup correlation analyses, moderation analyses were performed on gait–cognition pairs that showed significant or nominally significant correlations in the PDCN or PDMCI group. Linear regression models were constructed with the cognitive status (PDCN vs. PDMCI) as the moderator, the relevant gait parameter as the predictor, and the corresponding cognitive domain composite score as the outcome. An interaction term (gait parameter × cognitive status) was included to test whether the strength or direction of the association differed significantly between the two subgroups, with all models adjusted for age, sex, educational attainment, and mean leg length. All analyses were conducted using R software (v.4.4.3).

Results

Participant characteristics

A total of 124 participants (65 with PD and 59 HO) were enrolled in this study. Within the PD group, 38 patients were categorized as having PDCN and 27 as having PDMCI. In the two-group comparison, patients in the PD group were significantly younger and had lower educational attainment than those in the HO group. However, when comparing the three subgroups (HO, PDCN, and PDMCI), no significant differences were observed in terms of age, sex, mean leg length, or educational attainment. Within the PD group, the disease duration did not differ significantly between the PDCN and PDMCI groups.

In the assessments of global cognitive performance, the total K-MoCA score showed no significant differences between the PD and HO groups. However, a significant difference was observed in the orientation domain, with the PD group scoring lower. In the three-subgroup comparison, both the K-MoCA total score and the score for the orientation domain showed significant differences. The PDMCI group performed significantly worse than the HO group, whereas the PDCN group showed intermediate values that did not reach statistical significance. As expected from the cognitive-based classification, the PDMCI group performed significantly worse than the PDCN group across nearly all neuropsychological indices, with the exception of digit span forward and backward in the attention domain, as detailed in Supplementary Table 1. The demographic and clinical characteristics of the study population are summarized in Table 1.

Table 1

HO (N = 59)PD (N = 65)p value
AllPDCN
(N = 38)
PDMCI
(N = 27)
Age72.339 ± 7.51968.923 ± 5.50468.842 ± 6.15469.037 ± 4.5440.0191
Sex, M/F31/2828/3718/2010/170.3822
Leg length (cm)85.502 ± 4.48284.535 ± 4.65385.322 ± 4.20583.426 ± 5.0930.2423
Education (yr)11.627 ± 3.79610.138 ± 3.53910.526 ± 3.8829.593 ± 2.9780.0301
Disease duration (m)17.523 ± 18.87014.053 ± 13.94822.407 ± 23.6060.0531
K-MoCA26.644 ± 1.52923.776 ± 3.35025.267 ± 2.81521.421 ± 2.755a0.0984
 Visuospatial3.724 ± 0.5233.327 ± 0.9223.667 ± 0.6612.789 ± 1.0320.6184
 Attention5.672 ± 0.5745.184 ± 0.8585.300 ± 0.8375.000 ± 0.8820.8714
 Language4.793 ± 0.4094.571 ± 0.9134.767 ± 0.5044.263 ± 1.2840.0744
 Executive3.397 ± 0.5912.673 ± 1.1623.000 ± 0.9832.158 ± 1.2590.6754
 Memory3.052 ± 1.0991.796 ± 1.3992.400 ± 1.2760.842 ± 1.0150.1354
 Orientation5.983 ± 0.1315.939 ± 0.2425.933 ± 0.2545.947 ± 0.229a0.0054

Demographics and clinical characteristics of the study participants.

Values are presented as mean ± standard deviation for continuous variables and n for categorical variables. Normality was assessed using the Shapiro–Wilk test. Group differences between the HO and PD total groups were tested using Mann–Whitney 1U test, 2chi-square test, 3independent t-test, or 4ranked ANCOVA (adjusted for age, sex, and educational attainment). For comparisons among the three subgroups (HO, PDCN, and PDMCI), the Kruskal–Wallis test, chi-square test, ANOVA, or ranked ANCOVA (adjusted for age, sex, and educational attainment) were employed. Superscripts denote the statistical tests used. Bold values indicate statistically significant differences (p < 0.05) between the HO and PD total groups. aSignificant difference compared with the HO group. bSignificant difference between the PDCN and PDMCI groups.

HO, Healthy Older adults; K-MoCA, Korean-Montreal Cognitive Assessment; PD, Parkinson’s disease; PDCN, Parkinson’s disease with Cognitively Normal; PDMCI, Parkinson’s disease with Mild Cognitive Impairment.

Spatiotemporal gait parameters and dual-task cost

Across most gait parameters, the PD group demonstrated worse performance than the HO group, and this pattern became more pronounced under dual-task conditions. Specifically, under the cell phone use and backward-walking conditions, a greater number of parameters showed statistically significant group differences in comparison with the preferred speed condition, particularly within the pace and asymmetry domains. In contrast, the serial sevens subtraction condition yielded fewer significant between-group differences. Notably, certain parameters within the variability and postural control domains were worse in the HO group.

A similar pattern was observed for DTC. In comparison with the serial sevens subtraction condition (%Δ2–1), both the cell phone use (%Δ3–1) and backward-walking (%Δ4–1) conditions were associated with a greater number of parameters showing significant between-group differences. Furthermore, the directionality of the DTC, which reflected greater cognitive–motor interference in the PD group, was more consistently observed in the cell phone use condition. Overall, the cell phone use condition emerged as the most sensitive task, showing the greatest number of significant between-group differences across both spatiotemporal gait parameters and DTCs, as further illustrated in Figure 1. The spatiotemporal gait parameters and dual-task costs across the conditions are summarized in Tables 2, 3, respectively.

Figure 1

Table 2

PSSerial 7 sCPBW
HOPDpFDRHOPDpFDRHOPDpFDRHOPDpFDR
Pace
SV113.129 ± 22.649100.110 ± 25.1710.01099.926 ± 26.96689.176 ± 26.5850.13082.579 ± 24.10868.943 ± 22.9370.00376.465 ± 22.79957.128 ± 20.556<0.001
SL59.514 ± 9.78453.598 ± 10.1070.00254.606 ± 11.47749.213 ± 10.8910.06448.389 ± 10.35341.758 ± 10.129<0.00139.428 ± 10.87230.544 ± 10.029<0.001
SwiT sd0.021 ± 0.0090.023 ± 0.0150.7810.027 ± 0.0190.027 ± 0.0180.8620.042 ± 0.0340.054 ± 0.0460.0180.058 ± 0.0840.051 ± 0.0370.435
Variability
ST sd0.034 ± 0.0150.033 ± 0.0270.1120.039 ± 0.0390.040 ± 0.0540.8620.056 ± 0.0450.088 ± 0.0980.0160.057 ± 0.0610.060 ± 0.0390.084
StaT sd0.044 ± 0.0230.043 ± 0.0480.0890.048 ± 0.0620.060 ± 0.1070.8620.069 ± 0.0570.123 ± 0.1550.0160.059 ± 0.0290.074 ± 0.0440.060
SV sd7.908 ± 3.4176.691 ± 3.1600.0286.929 ± 2.5236.936 ± 2.8270.8957.944 ± 2.9918.435 ± 3.0480.34110.281 ± 3.2888.940 ± 3.2900.036
SL sd3.492 ± 1.6273.175 ± 1.4050.1443.550 ± 1.4303.380 ± 1.1850.8624.330 ± 2.0424.456 ± 1.6180.3386.569 ± 2.9535.524 ± 1.8340.031
Rhythm
ST0.541 ± 0.0550.554 ± 0.0700.7110.569 ± 0.0830.579 ± 0.1060.9340.611 ± 0.0930.645 ± 0.1190.1690.538 ± 0.0890.559 ± 0.1070.511
SwiT0.403 ± 0.0350.405 ± 0.0390.8670.413 ± 0.0500.407 ± 0.0570.5480.430 ± 0.0540.426 ± 0.0610.8510.370 ± 0.0680.366 ± 0.0690.762
StaT0.672 ± 0.0790.699 ± 0.1070.4950.720 ± 0.1300.750 ± 0.1720.8620.791 ± 0.1480.863 ± 0.2060.0760.705 ± 0.1190.750 ± 0.1570.271
Asymmetry
ST asy0.018 ± 0.0160.026 ± 0.0250.4950.020 ± 0.0200.030 ± 0.0310.1300.019 ± 0.0180.050 ± 0.045<0.0010.024 ± 0.0230.035 ± 0.0280.035
SwiT asy0.013 ± 0.0090.091 ± 0.1540.0150.013 ± 0.0110.093 ± 0.1590.0170.018 ± 0.0170.106 ± 0.154<0.0010.019 ± 0.0230.090 ± 0.129<0.001
StaT asy0.017 ± 0.0160.019 ± 0.0150.7110.016 ± 0.0140.018 ± 0.0160.8620.018 ± 0.0170.033 ± 0.0300.0060.021 ± 0.0160.029 ± 0.0220.057
Postural control
SL asy2.369 ± 1.6502.300 ± 1.8130.7812.687 ± 1.8432.395 ± 2.0420.5482.375 ± 1.7892.733 ± 2.6920.7223.260 ± 3.0104.804 ± 3.3250.011
SB9.722 ± 2.5699.717 ± 2.6170.8679.986 ± 2.8489.761 ± 2.7340.88010.025 ± 3.23910.089 ± 2.5410.61516.898 ± 4.07115.876 ± 3.4500.123
SB sd2.103 ± 0.7111.583 ± 0.501<0.0012.059 ± 0.5781.487 ± 0.512<0.0012.649 ± 0.7252.037 ± 0.797<0.0013.426 ± 1.3802.166 ± 0.867<0.001

Spatiotemporal gait parameters across task conditions between healthy older adults and patients with Parkinson’s disease.

Comparison of gait parameters between PD and healthy older adult groups across four task conditions: preferred speed, dual task-7, dual task-cell phone, and backward walking. Values are presented as means ± standard deviation, and group differences were tested using ranked ANCOVA adjusted for age, sex, leg length, and educational attainment. p-values were adjusted for multiple comparisons using the false discovery rate (FDR) method, and significant differences (FDR-adjusted p < 0.05) are indicated in bold.

Asy, asymmetry; BW, Backward walking; CP, Cell phone use; PS, Preferred Speed; SB, Support Base; sd, standard deviation; StaT, Stance Time; SL, Step Length; ST, Step Time; SV, Stride Velocity; SwiT, Swing Time.

Table 3

%Δ2–1%Δ3–1%Δ4–1
HOPDpFDRHOPDpFDRHOPDpFDR
Pace
SV−12.413 ± 11.995−11.648 ± 11.3530.872−27.835 ± 11.558−31.135 ± 15.4560.409−33.224 ± 12.262−43.303 ± 12.580<0.001
SL−8.693 ± 8.867−8.682 ± 7.9950.911−19.034 ± 9.745−22.270 ± 12.0790.085−34.489 ± 11.361−43.535 ± 12.605<0.001
SwiT sd35.762 ± 75.46430.975 ± 75.5270.872103.966 ± 144.286166.845 ± 181.0110.030225.443 ± 547.553178.905 ± 282.4100.603
Variability
ST sd14.559 ± 72.78032.186 ± 156.1320.74864.949 ± 106.403202.125 ± 287.1740.002105.759 ± 333.161123.215 ± 180.4630.011
StaT sd9.278 ± 81.22156.765 ± 228.7590.26562.343 ± 108.813238.596 ± 345.141<0.00152.649 ± 79.858148.855 ± 216.1400.011
SV sd−0.693 ± 48.58519.152 ± 67.2600.49715.345 ± 68.35144.696 ± 69.6410.00747.939 ± 66.46051.050 ± 73.6580.903
SL sd10.423 ± 43.61719.619 ± 55.7610.74835.651 ± 65.41956.527 ± 70.2320.059115.190 ± 122.60197.766 ± 96.4040.671
Rhythm
ST5.003 ± 8.3774.082 ± 10.2110.81212.877 ± 11.72816.329 ± 16.6060.502−0.474 ± 12.0170.797 ± 14.3120.806
SwiT2.481 ± 7.2700.233 ± 7.9540.2656.770 ± 10.5465.329 ± 11.6900.819−8.325 ± 13.785−9.720 ± 13.5900.712
StaT6.752 ± 10.8286.740 ± 13.5020.91217.352 ± 14.25423.509 ± 23.3350.4174.834 ± 12.0507.485 ± 16.2000.458
Asymmetry
ST asy108.850 ± 362.762124.567 ± 356.4760.83988.427 ± 213.026246.525 ± 401.3880.004238.068 ± 568.087293.374 ± 842.4480.811
SwiT asy121.638 ± 395.23454.802 ± 208.3590.839192.374 ± 467.188332.675 ± 1216.4080.417279.263 ± 703.600246.352 ± 627.9060.903
StaT asy50.381 ± 167.02769.419 ± 260.8920.748158.093 ± 455.487168.029 ± 260.8730.174242.799 ± 599.225289.027 ± 615.5710.335
Postural control
SL asy136.125 ± 472.668110.701 ± 454.4120.748122.246 ± 400.241121.915 ± 342.7420.544182.593 ± 441.999390.656 ± 790.0760.022
SB2.695 ± 15.6290.860 ± 12.6270.8393.269 ± 21.2425.772 ± 16.4190.41778.946 ± 41.99272.293 ± 51.2080.335
SB sd4.909 ± 32.339−0.561 ± 37.5600.74838.922 ± 54.78337.577 ± 66.2560.54472.341 ± 64.91552.640 ± 89.4350.022

Relative gait costs across task conditions between healthy older adults and patients with Parkinson’s disease.

%.

Dual task cost (DTC) was calculated as [(dual task - single task) / single task] × 100 (%). %Δ2–1 = serial 7 s subtraction; %Δ3–1 = cell phone use; %Δ4–1 = backward walking, each relative to single task. Values are presented as means ± standard deviation. Group differences were tested using ranked ANCOVA adjusted for age, sex, leg length and educational attainment. FDR-adjusted p-values are presented and significant values (p < 0.05) are shown in bold.

Asy, asymmetry; BW, Backward walking; CP, Cell phone use; PS, Preferred Speed; SB, Support Base; sd, standard deviation; StaT, Stance Time; SL, Step Length; ST, Step Time; SV, Stride Velocity; SwiT, Swing Time.

Partial correlation between gait and cognitive domains

Partial correlation analyses within the entire PD group revealed that both spatiotemporal gait parameters and DTCs were significantly associated with the five cognitive domains derived from the neuropsychological battery. Reflecting the prominent group differences observed in Tables 2, 3, these associations were most extensive during the cell phone use task, which demonstrated a consistently dominant correlation pattern across multiple domains after FDR correction. This finding was not merely attributable to the larger number of parameters included in this condition. Performance in the preferred speed condition was primarily linked to the attention domain. In contrast, gait during the cell phone use task showed a broader pattern of associations, correlating significantly with the attention, executive, and language domains. Under these conditions, pace-related parameters, including stride velocity and step length, were positively correlated with cognitive scores across multiple domains. Conversely, increased stance time, step time SD, step time, and swing-time asymmetry were negatively correlated with cognitive scores. Notably, swing-time asymmetry was the only gait parameter that was significantly correlated with the memory domain, and this association was observed across both the preferred speed and cell phone use conditions.

Regarding DTC, the correlation patterns showed a more concentrated distribution, primarily within the executive and language domains. The DTC for step length showed significant positive correlations with both executive and language domains. Furthermore, the higher costs associated with step time SD and stance time SD were consistently linked to lower scores in the executive and language domains. The correlation results are presented in Table 4.

Table 4

rpfdr
Spatiotemporal gait parameters
SV_ps – attention domain0.3360.045
SL_ps – attention domain0.3420.045
SwiTasy_ps – attention domain−0.3290.045
SwiTasy_ps – memory domain−0.3370.045
SwiTasy_ps – visuospatial domain−0.3790.045
SV_cp – executive domain0.4090.048
SV_cp – language domain0.3430.049
SV_cp – attention domain0.3370.049
SL_cp – executive domain0.3350.049
SL_cp – language domain0.3700.049
SL_cp – attention domain0.3250.049
STsd_cp – executive domain−0.3260.049
StaT_cp – executive domain−0.3550.049
STasy_cp – attention domain−0.3400.049
SwiTasy_cp – memory domain−0.3360.049
SV_bw – attention domain0.4080.040
Dual-task cost parameters
SL_DTCcp - executive domain0.3910.017
SL_DTCcp - language domain0.3560.027
StaTsd_DTCcp - executive domain−0.4310.014
StaTsd_DTCcp - language domain−0.3640.027
STsd_DTCcp - executive domain−0.4090.015
STsd_DTCcp - language domain−0.3500.027

Partial Spearman correlations between spatiotemporal gait parameters, dual-task costs, and cognitive domain scores in patients with Parkinson’s disease.

Partial Spearman correlations were performed between gait parameters showing significant group differences and neuropsychological test scores in PD patients (n = 65), controlling for age, sex, and leg length. p-values were corrected using the FDR method within each condition separately. Only significant correlations (FDR-adjusted p < 0.05) are presented.

Asy, asymmetry; cp, cell phone use; DTC, dual-task cost; sd, standard deviation; StaT, Stance Time; SL, Step Length; ST, Step Time; SV, Stride Velocity; SwiT, Swing Time.

Beyond the within-PD analyses, gait–cognition associations were examined in both the PD and HO groups using the domain-specific subscores of the K-MoCA to provide a broader comparative perspective. In the PD group, significant associations were observed across multiple gait parameters, predominantly within the language, attention, and executive domains, and were most evident during the preferred speed and cell phone use conditions. In the HO group, significant gait–cognition pairs were less frequent overall but were nonetheless present, with associations most evident in the attention, visuospatial, and executive domains, particularly during cell phone use and backward-walking conditions. These correlation patterns are shown in Figure 2.

Figure 2

As a secondary exploratory analysis, to examine whether cognitive status further modulated gait–cognition associations within the PD group, partial correlations were conducted separately for the PDCN and PDMCI groups using spatiotemporal gait parameters that showed significant differences between the two subgroups. These analyses revealed distinct cognitive–motor profiles, with the specific domains and directionality of associations differing markedly between the two groups. In the PDCN group, significant associations were sparse overall and were primarily concentrated within the visuospatial domain during the cell phone use task. Notably, better visuospatial performance was paradoxically associated with both increased gait variability (higher step time SD and stance time SD) and reduced stride velocity. In contrast, the executive domain in the PDCN group showed a more expected relationship, where better executive function was linked to improved gait performance, as reflected by the reduced stance time and step-length asymmetry. The PDMCI group showed a more extensive and widespread correlation pattern, wherein better performance across multiple cognitive domains, particularly the attention and visuospatial domains, was consistently associated with better gait stability. These subgroup-specific correlation patterns are shown in Figure 3 (nominal p < 0.05).

Figure 3

To determine whether the specific correlation patterns observed in the heatmaps were statistically driven by cognitive status rather than chance, a formal moderation analysis was performed on the previously identified significant pairs. This analysis aimed to verify whether the strength or direction of the gait–cognition associations were significantly different between the PDCN and PDMCI groups.

Moderation analysis confirmed that cognitive status significantly moderated several of these relationships even after adjusting for age, sex, educational attainment, and mean leg length. Specifically, the paradoxical associations observed in the PDCN group involving the visuospatial domain were found to be statistically distinct from the patterns observed in the PDMCI group (p < 0.05 for interaction terms), supporting the notion that the gait–cognition coupling pattern is fundamentally altered in relation to the cognitive status. The moderation effects and associated interaction terms are summarized in Table 5.

Table 5

Gait parameterCognitive domainTaskInteraction β (SE)p value
Pace
SVVisuospatialPreferred speed16.00 (6.38)0.015
VisuospatialSerial 7 s subtractions19.20 (6.65)0.006
VisuospatialCell phone use16.20 (5.79)0.008
SLVisuospatialSerial 7 s subtractions5.80 (2.67)0.034
VisuospatialCell phone use5.28 (2.43)0.034
SwiTsdVisuospatialCell phone use−0.03 (0.01)0.040
Variability
STsdLanguageCell phone use−0.06 (0.02)0.026
VisuospatialCell phone use−0.05 (0.03)0.049
StaTsdLanguageCell phone use−0.09 (0.04)0.016
Asymmetry
STasyVisuospatialCell phone use−0.03 (0.01)0.009
SwiTasyExecutiveBackward walking−0.13 (0.05)0.014
Postural control
SLasyExecutiveBackward walking3.15 (1.30)0.018

Moderation effects of cognitive status on the relationship between cognitive domains and gait parameters.

Only significant interactions (p < 0.05) are presented. β represents the interaction term (Cognitive Domain × Group), indicating the difference in slopes between PDCN and PDMCI (Reference: PDCN). All models were adjusted for age, sex, educational attainment, and mean leg length.

asy, asymmetry; sd, standard deviation; StaT, Stance Time; SL, Step Length; ST, Step Time; SV, Stride Velocity; SwiT, Swing Time.

Discussion

This study examined spatiotemporal gait performance and its relationship with cognitive function in individuals with early-stage PD and HO, with the aim of characterizing not only group-level differences in gait, but also how gait–cognition associations differed between the two groups and within the PD group in relation to cognitive status. Gait impairments in PD were more pronounced under dual-task conditions, with the cell phone use task emerging as the most sensitive condition in this sample. Gait–cognition associations within the PD group were most extensive during this condition, predominantly involving the executive, language, and attention domains. Furthermore, distinct cognitive–motor profiles were observed between PDCN and PDMCI, suggesting that cognitive status may qualitatively modulate the nature of gait–cognition interactions in PD.

Dual-task conditions and cognitive–motor interference

In comparison with single-task walking, dual-task conditions revealed more pronounced between-group differences, particularly within the pace, variability, and asymmetry domains, and most consistently in the cell phone use task. This is consistent with the concept of limited resource-capacity sharing (Tombu and Jolicoeur, 2003), in the addition of a secondary cognitive or motor task competes for the same neural resources required for locomotion. In healthy individuals, walking is largely automatized and requires minimal attentional resources (Clark, 2015). However, in PD, the degeneration of basal ganglia circuitry disrupts the automaticity of gait, increasing its dependence on cortical attentional networks (Kelly et al., 2012). Consequently, when a concurrent task is introduced, individuals with PD are less able to sustain gait performance, causing disproportionate deterioration in comparison with HO (Kusleikiene et al., 2025).

Visualization of spatiotemporal gait parameters and DTCs as Z-scores referenced to the HO group revealed that the swing-time asymmetry showed the largest deviation between the groups. Notably, the swing-time asymmetry already differed significantly between the groups under the preferred speed condition; as a result, the additional increment attributable to dual-task interference, as reflected in the DTC, was comparatively modest. In contrast, the variability domain parameters showed more prominent differences in DTC, suggesting that gait variability is more susceptible to cognitive–motor loading than asymmetry. As previously demonstrated in healthy populations, gait variability is considered a sensitive indicator of attentional resources engaged in motor control, with elevated variability reflecting a shift away from automatic locomotor processing toward more deliberate, attention-demanding control (Riedel et al., 2024). In this context, the disproportionate increase in gait variability observed in patients with PD under dual-task conditions may reflect a greater reliance on attentional resources to maintain locomotion, underscoring its clinical relevance as a marker of cognitive–motor vulnerability. Taken together, even after adjusting for age, sex, and leg length, individuals with early-stage PD demonstrated disease-specific gait alterations in comparison with HO, and these differences were further amplified when concurrent cognitive and motor demands were imposed.

Cell phone use as the most sensitive dual-task condition

Among the four walking conditions examined, the cell phone use task consistently produced the greatest number of significant between-group differences in the spatiotemporal gait parameters and DTCs. Cell phone use has become an inseparable part of contemporary life and is frequently employed during locomotion in everyday settings, such as commuting and transit. Previous studies have demonstrated that cell phone use during walking increases DTCs across multiple spatiotemporal gait parameters, even in children and young adults (Lee and Shin, 2024), underscoring the substantial cognitive–motor demands imposed by this activity. Unlike the serial sevens subtraction task, which is a purely cognitive secondary task with variable performance across individuals, the cell phone use task simultaneously imposes cognitive and motor demands, requiring visual attention, manual dexterity, and cognitive processing. This multicomponent nature, combined with the ecological validity of cell phone use as a ubiquitous daily-life activity, may render this task particularly sensitive to the limited resource capacity of individuals with PD. This is consistent with previous studies demonstrating that cell phone use during walking produces the most pronounced gait impairments among daily-life dual tasks in patients with PD (Yamada et al., 2020). This pattern is further supported by evidence from healthy older adults showing that combined cognitive–motor dual-task conditions produce disproportionately greater gait impairments than either cognitive or motor tasks alone (Nedović et al., 2024; Nedović et al., 2025). These observations suggest that the cell phone use condition may serve as a clinically useful dual-task paradigm in the assessment of cognitive–motor function in PD, though replication in larger and more diverse cohorts is warranted.

Paradoxical findings in variability and postural control domains

Interestingly, certain parameters within the variability and postural control domains were paradoxically higher in the HO group than in the PD group. This unexpected finding warrants careful interpretation. The participants with PD in the present study were significantly younger than those in the HO group and were in the early stages of the disease, with minimal postural instability. Postural instability and increased gait variability in PD tend to emerge and worsen with disease progression, indicating that these deficits may not yet fully manifest in early-stage patients. Furthermore, since age is a potent and independent determinant of gait variability (Mukli et al., 2025), the significant age difference between the two groups likely exerted a dominant influence on these specific metrics. Although age, sex, and leg length were included as covariates in the statistical models, the residual influence of age-related physiological changes in the HO group may not have been eliminated. Thus, in the early stages of PD, the influence of normal aging on gait variability and postural control can be more pronounced than that of disease-specific alterations. Collectively, these findings highlight that gait in patients with early PD reflects a complex interplay of disease-related and demographic factors, underscoring the need to interpret between-group differences within the context of the underlying cohort characteristics.

Gait–cognition associations and cognitive domain specificity

Within the total PD group, partial correlation analyses revealed significant associations between gait parameters and neuropsychological domains, most prominently during the cell phone use task, in which significant correlations were observed with the executive, language, and attention domains. The predominance of attention and executive function in gait–cognition associations is consistent with a substantial body of literature implicating prefrontal circuits in the regulation of dual-task gait (Clark, 2015; Ohsugi et al., 2013; Doi et al., 2013). Prefrontal circuits are known to be functionally compromised in patients with PD, partly as a consequence of disrupted basal ganglia-cortical connectivity (Hjelle et al., 2025), and their dysfunction may underlie both the attentional deficits and gait deterioration observed in this population. The involvement of the language domain is another notable finding, since language processing shares neural substrates with executive function and working memory (De Baene et al., 2015), and this finding may reflect the broader cognitive demands imposed by the cell phone use task. Regarding DTC, correlations were concentrated within the executive and language domains, suggesting that the ability to maintain gait performance under dual-task conditions is particularly sensitive to frontal lobe integrity in patients with PD.

Importantly, the pattern of gait–cognition associations differed between the PD and HO groups when examined using domain-specific subscores derived from the K-MoCA. While the PD group demonstrated associations spanning multiple cognitive domains, the HO group showed a more limited and circumscribed pattern of correlations confined to the attention, visuospatial, and executive domains during the cell phone use and backward-walking conditions. This observation suggests that the coupling between gait and cognition is not exclusive to pathological conditions, but is also present in healthy aging, albeit in a more limited fashion. The broader and more extensive gait–cognition associations observed in PD likely reflect the amplified dependence on cognitive resources for locomotor control that accompanies neurodegeneration.

Subgroup differences: exploratory cognitive–motor profiles between PDCN and PDMCI

In the subgroup analysis, the PDMCI group, as anticipated, exhibited more extensive gait–cognition associations than the PDCN group, and the specific domains and directionality of these associations differed markedly between the two groups, suggesting that cognitive status may qualitatively modulate the nature of cognitive–motor interactions in PD, though these findings should be interpreted with caution given the exploratory nature of the subgroup analysis and the modest sample sizes involved.

Of particular interest was the pattern observed in the PDCN group during the cell phone use task. Better visuospatial function is notably associated with increased gait variability. While seemingly counterintuitive, this divergent pattern may suggest a potential shift in resource allocation, possibly reminiscent of a posture-second strategy in which visuospatial resources are preferentially directed toward the cell phone use task at the expense of gait stability (Yogev-Seligmann et al., 2012). Notably, this pattern contrasts with prior studies reporting posture-second strategies primarily in individuals with MCI (Johansson et al., 2021) and may reflect the fact that such a flexible, though potentially destabilizing, re-allocation of resources requires sufficient cognitive reserve (Huxhold et al., 2006). Conversely, stronger executive function in the PDCN group was associated with improved gait stability, a finding consistent with prior evidence implicating the prefrontal cortex in both executive cognitive control and the regulation of locomotion under dual-task conditions (Holtzer et al., 2011; Patel et al., 2014). Thus, preserved executive resources may facilitate gait coordination even in the presence of competing task demands. Therefore, the dissociation between visuospatial and executive correlates in PDCN suggests that these two cognitive domains may relate to locomotor control in qualitatively different ways during cognitively demanding tasks, a finding that remains preliminary and warrants further investigation into the domain-specific mechanisms underlying cognitive–motor interactions in early PD.

In contrast, the PDMCI group showed a broader and more consistent pattern of positive correlations between gait stability and performance across multiple cognitive domains. This may indicate that locomotor control had become increasingly dependent on a wider range of cognitive resources, possibly reflecting a more vulnerable cognitive–motor system in which gait stability is more closely tied to overall cognitive capacity. While these findings could be interpreted in the context of task prioritization, direct evidence for such strategies would require the concurrent measurement of secondary task performance. Although the absence of cognitive cost measurements limited our ability to definitively conclude a specific postural prioritization strategy, the addition of a formal moderation analysis provided preliminary statistical support for these exploratory findings. The significant interaction effects suggested that the paradoxical association between visuospatial function and several gait parameters in the PDCN group may represent a statistically distinct pattern from that of the PDMCI group. Taken together, these results suggest that cognitive status may meaningfully modulate the gait–cognition coupling pattern, potentially reflecting a shift in locomotor control strategies as cognitive impairment emerges in PD. Replication in larger, well-characterized cohorts is nonetheless needed before firm conclusions can be drawn.

The present study has several limitations that require consideration. First, the cross-sectional design precluded causal inferences regarding the directionality of the gait–cognition associations. Second, the PD group represented patients at an early stage of the disease, which may limit the generalizability of the findings to patients with advanced PD. Third, despite covariate adjustment, the significant age difference between the PD and HO groups may have influenced some of the observed patterns, particularly within the variability and postural control domains. Fourth, the medication status was not systematically controlled across all participants, and dopaminergic effects on gait and cognition could not be fully excluded. Fifth, the subgroup analyses comparing PDCN and PDMCI were exploratory in nature, and the relatively small sample sizes within each subgroup warrant caution when interpreting these findings. Sixth, secondary task performance data during the cell phone use condition, such as typing accuracy, completion rate, and response speed, were not recorded. The absence of such data limits our ability to determine whether the observed gait changes reflect genuine cognitive-motor interference, differences in task prioritization strategies, variability in smartphone familiarity across participants, or individual differences in subjective cognitive load. Future longitudinal studies with larger, well-characterized cohorts are needed to replicate the exploratory subgroup and moderation findings reported here, clarify the temporal relationships between gait deterioration and cognitive decline in PD, and further evaluate the clinical utility of dual-task gait assessment, particularly the cell phone use paradigm, as a sensitive marker of cognitive–motor decline in early PD. Future studies should also incorporate simultaneous monitoring of both gait and secondary task performance to enable more comprehensive interpretation of cognitive-motor dual-task findings.

Statements

Data availability statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Ethics statement

The studies involving humans were approved by Ethics Committee of the Dong-A University Hospital. The studies were conducted in accordance with the local legislation and institutional requirements. The participants provided their written informed consent to participate in this study. Written informed consent was obtained from the individual(s) for the publication of any potentially identifiable images or data included in this article.

Author contributions

BJ: Formal analysis, Data curation, Writing – original draft. S-MC: Project administration, Supervision, Methodology, Investigation, Writing – review & editing, Conceptualization, Resources.

Funding

The author(s) declared that financial support was not received for this work and/or its publication.

Conflict of interest

The author(s) declared that this work was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Generative AI statement

The author(s) declared that Generative AI was not used in the creation of this manuscript.

Any alternative text (alt text) provided alongside figures in this article has been generated by Frontiers with the support of artificial intelligence and reasonable efforts have been made to ensure accuracy, including review by the authors wherever possible. If you identify any issues, please contact us.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Supplementary material

The Supplementary material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fnagi.2026.1896308/full#supplementary-material

References

  • 1

    AliP.DinomaisM.LabriffeM.Pieruccini-FariaF.Montero-OdassoM.BarthaR.et al. (2025). Mapping the neural substrate of high dual-task gait cost in older adults across the cognitive spectrum. Brain Struct. Funct.230:25. doi: 10.1007/s00429-024-02873-6,

  • 2

    AmaraA. W.WoodK. H.MiftenA. M.KleinschmidtL.WhiteC. S.JoopA.et al. (2025). Gait and balance dysfunction are associated with cognitive performance only in men with Parkinson's disease. Clin. Park. Relat. Disord.13:100363. doi: 10.1016/j.prdoa.2025.100363

  • 3

    AmboniM.BaroneP.HausdorffJ. M. (2013). Cognitive contributions to gait and falls: evidence and implications. Mov. Disord.28, 15201533. doi: 10.1002/mds.25674,

  • 4

    AmboniM.RicciardiC.CuocoS.DonisiL.VolzoneA.RicciardelliG.et al. (2022). Mild cognitive impairment subtypes are associated with peculiar gait patterns in Parkinson's disease. Front. Aging Neurosci.14:781480. doi: 10.3389/fnagi.2022.781480,

  • 5

    ClarkD. J. (2015). Automaticity of walking: functional significance, mechanisms, measurement and rehabilitation strategies. Front. Hum. Neurosci.9:246. doi: 10.3389/fnhum.2015.00246,

  • 6

    De BaeneW.DuyckW.BrassM.CarreirasM. (2015). Brain circuit for cognitive control is shared by task and language switching. J. Cogn. Neurosci.27, 17521765. doi: 10.1162/jocn_a_00817

  • 7

    Di FilippoF.De BiasiG.RussoM.RicciardiC.PisaniN.VolzoneA.et al. (2025). Dual-task-related gait patterns as possible marker of precocious and subclinical cognitive alterations in Parkinson disease. Sci. Rep.15:3371. doi: 10.1038/s41598-025-85118-8,

  • 8

    DoiT.MakizakoH.ShimadaH.ParkH.TsutsumimotoK.UemuraK.et al. (2013). Brain activation during dual-task walking and executive function among older adults with mild cognitive impairment: a fNIRS study. Aging Clin. Exp. Res.25, 539544. doi: 10.1007/s40520-013-0119-5,

  • 9

    GalnaB.LordS.BurnD. J.RochesterL. (2015). Progression of gait dysfunction in incident Parkinson's disease: impact of medication and phenotype. Mov. Disord.30, 359367. doi: 10.1002/mds.26110

  • 10

    GoldmanJ. G.WeisH.StebbinsG.BernardB.GoetzC. G. (2012). Clinical differences among mild cognitive impairment subtypes in Parkinson's disease. Mov. Disord.27, 11291136. doi: 10.1002/mds.25062,

  • 11

    GonzalezM. C.DalenI.Maple-GrødemJ.TysnesO. B.AlvesG. (2022). Parkinson's disease clinical milestones and mortality. NPJ Parkinsons Dis.8:58. doi: 10.1038/s41531-022-00320-z

  • 12

    HjelleN.MohantyB.HubbardT.JohnsonM. D.WangJ.JohnsonL. A.et al. (2025). Impairment of neuronal activity in the dorsolateral prefrontal cortex occurs early in parkinsonism. Front. Neurosci.19:1521443. doi: 10.3389/fnins.2025.1521443,

  • 13

    HoltzerR.MahoneyJ. R.IzzetogluM.IzzetogluK.OnaralB.VergheseJ. (2011). FNIRS study of walking and walking while talking in young and old individuals. J. Gerontol. A Biol. Sci. Med. Sci.66, 879887. doi: 10.1093/gerona/glr068,

  • 14

    HuxholdO.LiS. C.SchmiedekF.LindenbergerU. (2006). Dual-tasking postural control: aging and the effects of cognitive demand in conjunction with focus of attention. Brain Res. Bull.69, 294305. doi: 10.1016/j.brainresbull.2006.01.002,

  • 15

    JohanssonH.EkmanU.RennieL.PetersonD. S.LeavyB.FranzénE. (2021). Dual-task effects during a motor-cognitive task in Parkinson's disease: patterns of prioritization and the influence of cognitive status. Neurorehabil. Neural Repair35, 356366. doi: 10.1177/1545968321999053,

  • 16

    KangY.ParkJ. S.YuK. H.LeeB. C. (2009). A reliability, validity, and normative study of the Korean-Montreal cognitive assessment (K-MoCA) as an instrument for screening of vascular cognitive impairment. Korean J. Clin. Psychol.28, 549562. doi: 10.15842/kjcp.2009.28.2.013

  • 17

    KellyV. E.EusterbrockA. J.Shumway-CookA. (2012). A review of dual-task walking deficits in people with Parkinson’s disease: motor and cognitive contributions, mechanisms, and clinical implications. Parkinsons Dis.2012:918719. doi: 10.1155/2012/918719

  • 18

    KusleikieneS.PukenasK.Drozdova StatkevicieneM.ZivG.VintsW. A. J.MasiulisN.et al. (2025). Relationship between balance automaticity and dual-task interference in older adults. Mot. Control.30, 100116. doi: 10.1123/mc.2025-0014,

  • 19

    LeeY.ShinS. (2024). Risk of using smartphones while walking for digital natives in realistic environments: effects of cognitive-motor interference. Heliyon10:e28901. doi: 10.1016/j.heliyon.2024.e28901,

  • 20

    LitvanI.GoldmanJ. G.TrösterA. I.SchmandB. A.WeintraubD.PetersenR. C.et al. (2012). Diagnostic criteria for mild cognitive impairment in Parkinson's disease: Movement Disorder Society task force guidelines. Mov. Disord.27, 349356. doi: 10.1002/mds.24893,

  • 21

    MiyamotoM.MiyamotoT. (2022). Montreal cognitive assessment predicts the short-term risk of Lewy body disease in isolated REM sleep behavior disorder with reduced MIBG scintigraphy. Mov. Disord. Clin. Pract.10, 3241. doi: 10.1002/mdc3.13569,

  • 22

    MonaghanA. S.RagothamanA.HarkerG. R.Carlson-KuhtaP.HorakF. B.PetersonD. S. (2023). Freezing of gait in Parkinson's disease: implications for dual-task walking. J. Parkinsons Dis.13, 10351046. doi: 10.3233/jpd-230063,

  • 23

    MsigwaS. S.HongS.MkwambeM. C.MarealleE.ZhangX.WangJ. Y. (2026). Dual-task gait cognitive-motor interference as a marker of cognitive impairment in Parkinson's disease: a systematic review and meta-analysis. Mov. Disord. Clin. Pract.13, 876888. doi: 10.1002/mdc3.70409,

  • 24

    MukliP.MuranyiM.LipeczÁ.SzarvasZ.CsípőT.UngvariA.et al. (2025). Age-related and dual task-induced gait alterations and asymmetry: optimizing the Semmelweis study gait assessment protocol. Geroscience47, 69556983. doi: 10.1007/s11357-025-01722-6,

  • 25

    NedovićN.EminovićF.MarkovićV.StankovićI.RadovanovićS. (2024). Gait characteristics during dual-task walking in elderly subjects of different ages. Brain Sci.14:148. doi: 10.3390/brainsci14020148,

  • 26

    NedovićN.Mutavdžin KrnetaS.JovanovićS.VujičićD.KozincŽ.SkvortsovD. (2025). Dual task gait analysis: combined cognitive motor demands most severely impact walking patterns and joint kinematics. Life15:1009. doi: 10.3390/life15071009,

  • 27

    OhsugiH.OhgiS.ShigemoriK.SchneiderE. B. (2013). Differences in dual-task performance and prefrontal cortex activation between younger and older adults. BMC Neurosci.14:10. doi: 10.1186/1471-2202-14-10,

  • 28

    PatelP.LamarM.BhattT. (2014). Effect of type of cognitive task and walking speed on cognitive-motor interference during dual-task walking. Neuroscience260, 140148. doi: 10.1016/j.neuroscience.2013.12.016,

  • 29

    PostumaR. B.BergD.SternM.PoeweW.OlanowC. W.OertelW.et al. (2015). MDS clinical diagnostic criteria for Parkinson's disease. Mov. Disord.30, 15911601. doi: 10.1002/mds.26424,

  • 30

    RiedelN.HerzogM.SteinT.DemlB. (2024). Cognitive-motor interference during walking with modified leg mechanics: a dual-task walking study. Front. Psychol.15:1375029. doi: 10.3389/fpsyg.2024.1375029,

  • 31

    TombuM.JolicoeurP. (2003). A central capacity sharing model of dual-task performance. J. Exp. Psychol. Hum. Percept. Perform.29, 318. doi: 10.1037/0096-1523.29.1.3,

  • 32

    VergheseJ.RobbinsM.HoltzerR.ZimmermanM.WangC.XueX.et al. (2008). Gait dysfunction in mild cognitive impairment syndromes. J. Am. Geriatr. Soc.56, 12441251. doi: 10.1111/j.1532-5415.2008.01758.x,

  • 33

    YamadaP. A.Amaral-FelipeK. M.SpinosoD. H.AbreuD. C. C.Stroppa-MarquesA. E. Z.Faganello-NavegaF. R. (2020). Everyday tasks impair spatiotemporal variables of gait in older adults with Parkinson's disease. Hum. Mov. Sci.70:102591. doi: 10.1016/j.humov.2020.102591

  • 34

    Yogev-SeligmannG.HausdorffJ. M.GiladiN. (2008). The role of executive function and attention in gait. Mov. Disord.23, 329342. doi: 10.1002/mds.21720,

  • 35

    Yogev-SeligmannG.HausdorffJ. M.GiladiN. (2012). Do we always prioritize balance when walking? Towards an integrated model of task prioritization. Mov. Disord.27, 765770. doi: 10.1002/mds.24963,

  • 36

    YooD.LeeJ. Y.KimY. K.YoonE. J.KimH.KimR.et al. (2021). Mild cognitive impairment and abnormal brain metabolic expression in idiopathic REM sleep behavior disorder. Parkinsonism Relat. Disord.90, 17. doi: 10.1016/j.parkreldis.2021.07.022,

  • 37

    ZhangW.LingY.ChenZ.RenK.ChenS.HuangP.et al. (2024). Wearable sensor-based quantitative gait analysis in Parkinson's disease patients with different motor subtypes. NPJ Digit. Med.7:169. doi: 10.1038/s41746-024-01163-z,

Summary

Keywords

cognitive-motor associations, dual-task gait, gait analysis, mild cognitive impairment, Parkinson’s disease

Citation

Jin B and Cheon S-M (2026) Dual-task gait and gait-cognition coupling in patients with Parkinson’s disease versus healthy older adults: moderation by cognitive status. Front. Aging Neurosci. 18:1896308. doi: 10.3389/fnagi.2026.1896308

Received

31 May 2026

Revised

23 July 2026

Accepted

27 July 2026

Published

12 August 2026

Volume

18 - 2026

Edited by

Cynthia Sandor, Imperial College London, United Kingdom

Reviewed by

Mahmoud Seifallahi, Florida Atlantic University, United States

Nenad Nedovic, Academy for Applied Studies Belgrade (AASB), Serbia

Updates

Copyright

*Correspondence: Sang-Myung Cheon,

Disclaimer

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

Outline

Figures

Cite article

Copy to clipboard


Export citation file


Share article

Article metrics