| Literature DB >> 35446905 |
Javad Sarvestan1, Peyman Aghaie Ataabadi2, Zdeněk Svoboda1, Fatemeh Alaei1, Ryan B Graham3.
Abstract
Mobile phone use affects the dynamics of gait by impairing visual control of the surrounding environment and introducing additional cognitive demands. Although it has been shown that using a mobile phone alters whole-body dynamic stability, no clear information exists on its impacts on motor variability during gait. This study aimed at assessing the impacts of various types of mobile phone use on motor variability during gait; quantified using the short- and long-term Lyapunov Exponent (λS and λL) of lower limb joint angles and muscle activation patterns, as well as the centre of mass position. Fourteen females and Fifteen males (27.72 ± 4.61 years, body mass: 70.24 ± 14.13 Kg, height: 173.31 ± 10.97 cm) walked on a treadmill under six conditions: normal walking, normal walking in low-light, walking while looking at the phone, walking while looking at the phone in low-light, walking and talking on the phone, and walking and listening to music. Variability of the hip (p λS = .015, λL = .043) and pelvis (p λS = .039, λL = .017) joint sagittal angles significantly increased when the participants walked and looked at the phone, either in normal or in low-light conditions. No significant difference was observed in the variability of the centre of mass position and muscle activation patterns. When individuals walk and look at the phone screen, the hip and knee joints are constantly trying to adopt a new angle to regulate and maintain gait stability, which might put an additional strain on the neuromuscular system. To this end, it is recommended not to look at the mobile phone screen while walking, particularly in public places with higher risks of falls.Entities:
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Year: 2022 PMID: 35446905 PMCID: PMC9022869 DOI: 10.1371/journal.pone.0267476
Source DB: PubMed Journal: PLoS One ISSN: 1932-6203 Impact factor: 3.752
Fig 1Schematic representation of the estimation of the maximum finite-time Lyapunov exponent for the knee sagittal plane (left), rectus femoris activities (centre) and COM trajectories (right). The 3D reconstruction of the phase-space and the expanded view of the reconstructed phase-space (up), and the average logarithmic rate of divergence for λS and λL (down).
Descriptive measures of λS and λL for the ankle, knee, hip and pelvis angles, and the COM and their differences in various walking conditions in sagittal, frontal and horizontal planes.
| NW | WLP | WLL | WLLLP | WM | WTP |
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|---|---|---|---|---|---|---|---|---|---|---|
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| 1.167(.405) | 1.191(.296) | 1.091(.289) | 1.103(.239) | 1.152(.356) | 1.112(.309) | .772 | .572 |
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| .006(.004) | .006(.005) | .007(.005) | .006(.004) | .006(.006) | .006(.004) | .222 | .953 | ||
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| 1.309(.362) | 1.286(.329) | 1.254(.276) | 1.290(.310) | 1.259(.306) | 1.268(.283) | .168 | .974 | |
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| .006(.004) | .006(.003) | .006(.004) | .006(.005) | .005(.006) | .005(.004) | .436 | .823 | ||
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| 1.257(.392) | 1.227(.338) | 1.204(.331) | 1.278(.375) | 1.261(.328) | 1.223(.369) | .347 | .884 | |
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| .006(.003) | .006(.004) | .006(.004) | .005(.005) | .006(.003) | .006(.005) | .083 | .995 | ||
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| .991(.423) | 1.014(.0504) | 1.016(.505) | 1.007(.503) | 1.032(.509) | 1.039(.524) | .127 | .986 |
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| .008(.006) | .009(.006) | .008(.006) | .009(.008) | .009(.008) | .009(.007) | .097 | .992 | ||
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| 1.051(.403) | 1.097(.408) | 1.106(.349) | 1.119(.346) | 1.074(.423) | 1.112(.333) | .289 | .919 | |
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| .007(.005) | .008(.006) | .008(.006) | .008(.008) | .008(.007) | .007(.005) | .107 | .991 | ||
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| 1.177(.315) | 1.194(.319) | 1.218(.397) | 1.190(.363) | 1.193(.414) | 1.218(.357) | .142 | .982 | |
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| .005(.004) | .006(.004) | .006(.004) | .006(.003) | .005(.004) | .006(.004) | .191 | .966 | ||
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| .720 (.147) | .807(.247) | .725(.137) | .854(.188) | .721(.118) | .736(.136) | 8.588 |
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| .007(.005) | .012(.008) | .009(.007) | .013(.009) | .009(.007) | .008(.006) | 2.765 |
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| .876(.389) | .871(.372) | .903(.338) | .899(.370) | .872(.392) | .929(.318) | .235 | .947 | |
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| .005(.005) | .006(.007) | .006(.004) | .007(.007) | .006(.006) | .007(.006) | .215 | .956 | ||
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| 1.088(.307) | 1.030(.375) | 1.045(.277) | 1.087(.291) | 1.092(.319) | 1.014(.339) | .484 | .788 | |
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| .006(.008) | .006(.007) | .006(.005) | .007(.006) | .007(.006) | .007(.005) | .139 | .983 | ||
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| .843(.363) | .974(.389) | .893(.422) | 1.137(.489) | .889(.339) | .942(.418) | 2.666 |
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| .006(.004) | .012(.013) | .007(.006) | .013(.018) | .008(.004) | .008(.008) | 2.356 |
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| 1.167(.394) | 1.188(.385) | 1.156(.280) | 1.208(.324) | 1.180(.277) | 1.116(.234) | .329 | .825 | |
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| .007(.007) | .008(.011) | .007(.006) | .007(.006) | .008(.008) | .008(.009) | .130 | .985 | ||
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| .741(.212) | .749(.254) | .766(.175) | .733(.262) | .754(.204) | .799(.208) | .449 | .814 | |
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| .006(.005) | .008(.005) | .007(.006) | .007(.005) | .006(.005) | .007(.005) | .810 | .544 | ||
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| 1.015(.249) | .986(.243) | .961(.228) | .958(.216) | 1.028(.207) | 1.033(.241) | .758 | .581 |
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| .019(.012) | .020(.015) | .015(.012) | .016(.015) | .018(.010) | .019(.013) | .705 | .621 | ||
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| .866(.274) | .972(.225) | .944(.339) | .986(.243) | .980(.291) | .868(.236) | 1.279 | .276 | |
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| .022(.018) | .028(.022) | .027(.017) | .024(.019) | .023(.020) | .020(.015) | .878 | .497 | ||
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| 1.336(.251) | 1.331(.280) | 1.323(.240) | 1.363(.256) | 1.311(.290) | 1.284(.248) | .526 | .757 | |
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| .008(.009) | .007(.005) | .007(.006) | .008(.006) | .008(.006) | .007(.006) | .417 | .836 | ||
† Significantly different at α<0.05.
‡ Significantly different at α<0.01.
a significantly different with WLP at p < .001.
b significantly different with WLLLP at p < .001.
c significantly different with WTP at p < .001.
Note: Given the high number of conditions, we reported the differences only in one condition to prevent duplication. For instance, if the λ values for WN and WLP were significantly different, we reported that in the WN condition.
Descriptive measures of λS and λL for the RF, VM, GA, TA, BF, and GM and their differences in various walking conditions in sagittal, frontal and horizontal planes.
| NW | WLP | WLL | WLLLP | WM | WTP | F | p | ||
|---|---|---|---|---|---|---|---|---|---|
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| .805(.325) | .862(.351) | .868(.375) | .886(.473) | .938(.206) | .848(.187) | .576 | .718 |
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| .006(.004) | .007(.005) | .005(.004) | .007(.005) | .006(.006) | .005(.003) | 1.033 | .403 | |
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| .828(.338) | .839(.378) | .805(.351) | .866(.283) | .882(.171) | .950(.274) | .003 | .958 |
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| .006(.005) | .007(.006) | .006(.006) | .007(.006) | .006(.005) | .005(.004) | .794 | .556 | |
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| .863(.318) | .885(.397) | .905(.395) | .936(.322) | .948(.228) | .857(.300) | .836 | .368 |
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| .007(.004) | .006(.005) | .006(.005) | .006(.005) | .004(.004) | .005(.004) | .213 | .648 | |
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| .852(.356) | .821(.326) | .856(.391) | .910(.356) | .916(.227) | .895(.337) | .375 | .865 |
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| .005(.005) | .005(.004) | .005(.004) | .006(.005) | .004(.004) | .005(.005) | .580 | .715 | |
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| .846(.446) | .860(.422) | .826(.359) | .837(.323) | .948(.202) | .894(.368) | .480 | .790 |
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| .007(.009) | .007(.005) | .006(.005) | .007(.004) | .007(.005) | .006(.006) | .296 | .915 | |
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| .942(.352) | .884(.323) | .947(.444) | .924(.472) | .970(.262) | .878(.371) | .298 | .913 |
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| .006(.004) | .005(.005) | .007(.004) | .007(.006) | .005(.003) | .006(.006) | 1.172 | .326 |
RF = Rectus Femoris, VM = Vastus Medialis, GA = Gastrocnemious, TA = Tibialis Anterior, BF = Biceps Femoris, GM = Gluteus Medius.