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. 2022 Apr 11;12(1):6055.
doi: 10.1038/s41598-022-10101-6.

Effects of experimentally induced cervical spine mobility alteration on the postural organisation of gait initiation

Affiliations

Effects of experimentally induced cervical spine mobility alteration on the postural organisation of gait initiation

A Delafontaine et al. Sci Rep. .

Abstract

Gait initiation (GI), the transient period between quiet standing and locomotion, is a functional task classically used in the literature to investigate postural control. This study aimed to investigate the influence of an experimentally-induced alteration of cervical spine mobility (CSM) on GI postural organisation. Fifteen healthy young adults initiated gait on a force-plate in (1) two test conditions, where participants wore a neck orthosis that passively simulated low and high levels of CSM alteration; (2) one control condition, where participants wore no orthosis; and (3) one placebo condition, where participants wore a cervical bandage that did not limit CSM. Centre-of-pressure and centre-of-mass kinematics were computed based on force-plate recordings according to Newton's second law. Main results showed that anticipatory postural adjustments amplitude (peak backward centre-of-pressure shift and forward centre-of-mass velocity at toe-off) and motor performance (step length and forward centre-of-mass velocity at foot-contact) were altered under the condition of high CSM restriction. These effects of CSM restriction may reflect the implementation of a more cautious strategy directed to attenuate head-in-space destabilisation and ease postural control. It follows that clinicians should be aware that the prescription of a rigid neck orthosis to posturo-deficient patients could exacerbate pre-existing GI deficits.

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Conflict of interest statement

The authors declare no competing interests.

Figures

Figure 1
Figure 1
Typical biomechanical traces in the Control condition and the GI-high condition (gait initiation with a high level of cervical spine mobility restriction). Traces reported in each condition are obtained from the same participant performing one single trial. Anteroposterior (AP) direction. x’MTO, x’MFC: centre-of-mass (COM) velocity at toe-off and foot-contact. xPmax: peak of backward centre-of-pressure (COP) shift during APA. F forward; B backward. Mediolateral (ML) direction. y’MTO, y’MFC: COM velocity at toe-off and foot-contact. yPmax: peak of ML COP shift during APA. ST: stance limb; SW: swing limb. Vertical direction. z’Mmin, z’MFC: peak of negative vertical COM velocity and COM velocity at foot-contact. D downward; U upward. Vertical dashed lines: t0 onset variation of biomechanical traces; HO swing heel-off; TO swing toe-off, FC swing foot-contact. Horizontal arrows: QS quiet standing, APA anticipatory postural adjustments; FL: swing foot-lift; EXE execution phase of gait initiation.
Figure 2
Figure 2
Effects of the condition on selected APA and foot-lift parameters. Reported are mean values (all participants together) + 1 SD. APA anticipatory postural adjustments, AP anteroposterior, COP centre-of-pressure, COM centre-of-mass, TO swing toe-off; *, **: significant difference between bars with p < 0.05 and p < 0.01, respectively.
Figure 3
Figure 3
Effects of the condition on motor performance (upper panels) and stability parameters (bottom panels). Reported are mean values (all participants together) + 1 SD. AP, ML anteroposterior, mediolateral; COM centre-of-mass; FC foot-contact; *, **: significant difference between bars with p < 0.05 and p < 0.01, respectively.
Figure 4
Figure 4
Cervical collars used in the placebo condition (A; jersey tubular bandage), the GI-low condition (B; foam flexible orthosis) and the GI-high condition (C; rigid orthosis).

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