Abstract
The experiment was setup to investigate the control of human quiet standing through the manipulation of augmented visual information feedback of selective properties of the motion of two primary variables in postural control: center of pressure (COP) and center of mass (COM). Five properties of feedback information were contrasted to a no feedback dual-task (watching a movie) control condition to determine the impact of visual real-time feedback on the coordination of the joint motions in postural control in both static and dynamic one-leg standing postures. The feedback information included 2D COP or COM position and macro variables derived from the COP and COM motions, namely virtual time-to-contact (VTC) and the COP–COM coupling. The findings in the static condition showed that the VTC and COP–COM coupling feedback conditions decreased postural motion more than the 2D COP or COM positional information. These variables also induced larger sway amplitudes in the dynamic condition showing a more progressive search strategy in exploring the stability limits. Canonical correlation analysis (CCA) found that COP–COM coupling contributed less than the other feedback variables to the redundancy of the system reflected in the common variance between joint motions and properties of sway motion. The COP–COM coupling had the lowest weighting of the motion properties to redundancy under the feedback conditions but overall the qualitative pattern of the joint motion structures was preserved within the respective static and dynamic balance conditions.
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References
Bernstein NA (1967) The co-ordination and regulation of movements. Pergamon Press, New York
Brillinger DR (1975) Time series: data analysis and theory. Holt, Rinehart & Winston, New York
Creath R, Kiemel T, Horak F, Peterka R, Jeka J (2005) A unified view of quiet and perturbed stance: simultaneous co-existing excitable modes. Neurosci Lett 377:75–80. doi:10.1016/j.neulet.2004.11.071
Danna-Dos-Santos A, Degani AM, Zatsiorsky VM, Latash ML (2008) Is voluntary control of natural postural sway possible? J Mot Behav 40:179–185. doi:10.3200/JMBR.40.3.179-185
Dijkstra T, Schöner G, Gielen C (1994) Temporal stability of the action-perception cycle for postural control in a moving visual environment. Exp Brain Res 97:477–486
Donker SF, Roerdink M, Greven AJ, Beek PJ (2007) Regularity of center-of-pressure trajectories depends on the amount of attention invested in postural control. Exp Brain Res 181:1–11
Duarte M, Zatsiorsky VM (2002) Effects of body lean and visual information on the equilibrium maintenance during stance. Exp Brain Res 146:60–69. doi:10.1007/s00221-002-1154-1
Edwards A (1946) Body sway and vision. J Exp Psychol 36:526
Faugloire E, Bardy BG, Merhi O, Stoffregen TA (2005) Exploring coordination dynamics of the postural system with real-time visual feedback. Neurosci Lett 374:136–141. doi:10.1016/j.neulet.2004.10.043
Freides D (1974) Human information processing and sensory modality: cross-modal functions, information complexity, memory, and deficit. Psychol Bull 81:284. doi:10.1037/h0036331
Freitas SMSF, Duarte M (2012) Joint coordination in young and older adults during quiet stance: effect of visual feedback of the center of pressure. Gait Posture 35:83–87. doi:10.1016/j.gaitpost.2011.08.011
Goldie P, Bach T, Evans O (1989) Force platform measures for evaluating postural control: reliability and validity. Arch Phys Med Rehabil 70:510–517
Haddad JM, Gagnon JL, Hasson CJ, Van Emmerik RE, Hamill J (2006) Evaluation of time-to-contact measures for assessing postural stability. J Appl Biomech 22:155–161
Haibach PS, Slobounov SM, Slobounova ES, Newell KM (2007) Virtual time-to-contact of postural stability boundaries as a function of support surface compliance. Exp Brain Res 177:471–482. doi:10.1007/s00221-006-0703-4
Haken H (2006) Information and self-organization: a macroscopic approach to complex systems. Springer Science & Business Media, Heidelberg
Hillman CH, Rosengren KS, Smith DP (2004) Emotion and motivated behavior: postural adjustments to affective picture viewing. Biol Psychol 66:51–62. doi:10.1016/j.biopsycho.2003.07.005
Hof A, Gazendam M, Sinke W (2005) The condition for dynamic stability. J Biomech 38:1–8. doi:10.1016/j.jbiomech.2004.03.025
Horak FB, Nashner LM (1986) Central programming of postural movements: adaptation to altered support-surface configurations. J Neurophysiol 55:1369–1381
Hsu WL, Scholz JP, Schoner G, Jeka JJ, Kiemel T (2007) Control and estimation of posture during quiet stance depends on multijoint coordination. J Neurophysiol 97:3024–3035. doi:10.1152/jn.01142.2006
Huxhold O, Li S-C, Schmiedek F, Lindenberger U (2006) Dual-tasking postural control: aging and the effects of cognitive demand in conjunction with focus of attention. Brain Res Bull 69:294–305. doi:10.1016/j.brainresbull.2006.01.002
Kelso J (1995) The self-organization of brain and behavior. MIT Press, Cambridge
Kennedy MW, Crowell CR, Striegel AD, Villano M, Schmiedeler JP (2013) Relative efficacy of various strategies for visual feedback in standing balance activities. Exp Brain Res 230:117–125. doi:10.1007/s00221-013-3634-x
Kilby MC, Slobounov SM, Newell KM (2014) Postural instability detection: aging and the complexity of spatial-temporal distributional patterns for virtually contacting the stability boundary in human stance. PLoS One 9:e108905. doi:10.1371/journal.pone.0108905
Kilby MC, Molenaar PC, Newell KM (2015) Models of postural control: shared variance in joint and COM motions. PLoS One 10:e0126379. doi:10.1371/journal.pone.0126379
Kilby MC, Slobounov SM, Newell KM (2016) Augmented feedback of COM and COP modulates the regulation of quiet human standing relative to the stability boundary. Gait Posture 47:18–23
Kinsella-Shaw JM, Harrison SJ, Turvey M (2011) Interleg coordination in quiet standing: influence of age and visual environment on noise and stability. J Mot Behav 43:285–294
Ko JH, Challis JH, Newell KM (2014) Transition of COM–COP relative phase in a dynamic balance task. Hum Mov Sci 38:1–14. doi:10.1016/j.humov.2014.08.005
Lee D, Lishman JR (1975) Visual proprioceptive control of stance. J Human Mov Stud 1(2):87–95
Lobo I (2008) Biological complexity and integrative levels of organization. Nat Educ 1:141. doi:10.1126/science.101.2618.209
Mason PH (2015) Degeneracy: demystifying and destigmatizing a core concept in systems biology. Complexity 20:12–21. doi:10.1002/cplx.21534
Mitra S, Amazeen PG, Turvey MT (1998) Intermediate motor learning as decreasing active (dynamical) degrees of freedom. Hum Mov Sci 17:17–65. doi:10.1016/S0167-9457(97)00023-7
Murnaghan C, Horslen B, Inglis J, Carpenter M (2011) Exploratory behavior during stance persists with visual feedback. Neuroscience 195:54–59. doi:10.1016/j.neuroscience.2011.08.020
Nashner L (1989) Sensory, neuromuscular, and biomechanical contributions to human balance. In: Balance: Proceedings of the APTA Forum, Nashville, Tennessee, vol 512
Newell K, Carlton MJ (1987) Augmented information and the acquisition of isometric tasks. J Mot Behav 19:4–12. doi:10.1080/00222895.1987.10735397
Noble R, Smith EP, Ye K (2004) Model selection in canonical correlation analysis (CCA) using Bayesian model averaging. Environmetrics 15:291–311. doi:10.1002/env.641
Pei L, Li H, Fu Y, Yang Y, Li J (2013) Influences of visual feedback indicator scales on human upright postural control. Trans Inst Meas Control 35:883–892
Radhakrishnan SM, Hatzitaki V, Vogiannou A, Tzovaras D (2010) The role of visual cues in the acquisition and transfer of a voluntary postural sway task. Gait Posture 32:650–655
Riccio GE, Stoffregen TA (1988) Affordances as constraints on the control of stance. Hum Mov Sci 7:265–300
Slobounov S, Newell K (1994) Postural dynamics as a function of skill level and task constraints. Gait Posture 2:85–93
Slobounov SM, Slobounova ES, Newell KM (1997) Virtual time-to-collision and human postural control. J Mot Behav 29:263–281. doi:10.1080/00222899709600841
Slobounov S, Wu T, Hallett M, Shibasaki H, Slobounov E, Newell K (2006) Neural underpinning of postural responses to visual field motion. Biol Psychol 72:188–197. doi:10.1016/j.biopsycho.2005.10.005
Stoffregen TA, Pagulayan RJ, BtG Bardy, Hettinger LJ (2000) Modulating postural control to facilitate visual performance. Hum Mov Sci 19:203–220
Teasdale N, Simoneau M (2001) Attentional demands for postural control: the effects of aging and sensory reintegration. Gait Posture 14:203–210. doi:10.1016/S0966-6362(01)00134-5
Travis RC (1945) An experimental analysis of dynamic and static equilibrium. J Exp Psychol 35:216
Vuillerme N, Bertrand R, Pinsault N (2008) Postural effects of the scaled display of visual foot center of pressure feedback under different somatosensory conditions at the foot and the ankle. Arch Phys Med Rehabil 89:2034–2036. doi:10.1016/j.apmr.2008.03.017
Wade MG, Jones G (1997) The role of vision and spatial orientation in the maintenance of posture. Phys Ther 77:619–628
Walker C, Brouwer BJ, Culham EG (2000) Use of visual feedback in retraining balance following acute stroke. Phys Ther 80:886–895
Wang Z, Ko JH, Challis JH, Newell KM (2014) The degrees of freedom problem in human standing posture: collective and component dynamics. PLoS One 9:e85414. doi:10.1371/journal.pone.0085414
Whitacre JM (2010) Degeneracy: a link between evolvability, robustness and complexity in biological systems. Theor Biol Med Model 7:6
Winter DA, Prince F, Frank JS, Powell C, Zabjek KF (1996) Unified theory regarding A/P and M/L balance in quiet stance. J Neurophysiol 75:2334–2343
Wulf G (2007) Attention and motor skill learning. In: Human Kinetics p 211
Young W, Ferguson S, Brault S, Craig C (2011) Assessing and training standing balance in older adults: a novel approach using the ‘Nintendo Wii’Balance Board. Gait Posture 33:303–305. doi:10.1016/j.gaitpost.2010.10.089
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Appendices
Appendix A—virtual time-to-contact (VTC) in 2D space
Input data for VTC (Slobounov et al. 1997) calculation in MATLAB was the 2D position of the COP or COM along with the instantaneous velocity and acceleration vectors, respectively. The 2D stability boundary was defined as the outside edge of the foot namely the base of support and was modeled by projecting the markers placed at the distal phalanges, fifth metatarsal, lateral malleolus heel and medial malleolus onto the ground and connecting them with line segments.
VTC (τ) at each time instant is the time the COM or COP would need to contact with the 2D stability boundary if it were to continue from the current position (\( \overrightarrow {r} = \left[ {\mathop r\nolimits_{x} ,\mathop r\nolimits_{y} } \right]T \)) with instantaneous initial velocity (\( \overrightarrow {v} = \left[ {\mathop v\nolimits_{x} ,\mathop v\nolimits_{y} } \right]T \)) and instantaneous constant acceleration (\( \overrightarrow {a} = \left[ {\mathop a\nolimits_{x} ,\mathop a\nolimits_{y} } \right]T \)).
Let (x c , y c ) denote the point on the stability boundary where the virtual trajectory intersects it for the first time. If the end points of the corresponding boundary line segment are (x 1, y 1) and (x 2, y 2), the slope (s) of the line connecting the two points is
Assuming constant slope in the differential segment between (x 1, y 1) and (x 2, y 2), the slope can also be computed as
Assuming a point mass model for the COM and constant acceleration, the point of virtual contact can be written as,
Substituting x c and y c from Eqs. 3–4 in 2, and equating it to 1, gives a quadratic equation in τ. VTC (τ) is the lowest positive solution of this quadratic equation. In the case where both velocity and acceleration were zero, VTC would be infinity.
Appendix B—canonical correlation analysis (CCA)
Canonical correlation analysis (CCA) is a general approach that can reveal the linear structure between two sets of variables (Brillinger 1975). CCA is based on simultaneous singular value (eigenvalue) decomposition of two multivariate datasets in such a way that the component scores associated with the first eigenvector of the first dataset has maximum correlation with the component scores associated with the first eigenvector of the second dataset. Given the first eigenvectors, the component scores associated with the second eigenvectors (which are orthogonal to the first eigenvectors) again have maximum correlation, etc.
Let Set 1 with p variables and n observations be represented by a n × p random variable X and set 2 with q variables and n observations by a n × q random variable Y. CCA creates d = min (rank(X), rank(Y)) pairs of n × 1 linear combinations (=component scores) U and V of the original variables from each set:
where i = 1,…, d, a i and b i are p × 1 and q × 1 coefficient vectors. Let S be the total (p + q, p + q) dimensional variance–covariance matrix of X (set 1) and Y (set 2):
Using singular value decomposition the eigenvalues in decreasing order and the corresponding eigenvectors of
are obtained. The ith eigenvector of A p constitutes the a i coefficients and the ith eigenvector of A q the b i coefficients. The canonical correlations are derived from the first d eigenvalues λ i . The canonical correlation r i is the square root of λ i . The eigenvalues of A p and A q are the same, and either one can be used to obtain the canonical correlation.
CCA was performed using standardized data; therefore, S can be replaced by the correlation matrix ρ. A pair of component scores associated with the ith eigenvectors of the two sets is commonly termed the ith canonical function. The significance of each canonical function (pairs of U and V) was assessed using F-statistics.
The CCA cross-loadings are the bivariate correlations between each original variable and the component score of the other set. There are no general guidelines for distinguishing high versus low cross-loadings (Noble et al. 2004). Therefore, the interpretation of the cross-loadings is kept at a qualitative level. The CCA redundancy index of each set can be obtained by multiplying the average proportion of total variance by the squared canonical correlation coefficient.
The CCA redundancy index can also be obtained by averaging the squared cross-loadings. It quantifies the amount of variance represented by the component score associated with the ith eigenvector of set 1 that can be explained by the component score associated with the ith eigenvector of set 2 and vice versa. Similar to R 2 in multiple regression it is the shared variance between the two sets.
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Kilby, M.C., Molenaar, P.C.M., Slobounov, S.M. et al. Real-time visual feedback of COM and COP motion properties differentially modifies postural control structures. Exp Brain Res 235, 109–120 (2017). https://doi.org/10.1007/s00221-016-4769-3
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DOI: https://doi.org/10.1007/s00221-016-4769-3