TY - JOUR
T1 - Unraveling stroke gait deviations with movement analytics, more than meets the eye
T2 - a case control study
AU - Pan, Jing Wen
AU - Sidarta, Ananda
AU - Wu, Tsung Lin
AU - Kwong, Wai Hang Patrick
AU - Ong, Poo Lee
AU - Tay, Matthew Rong Jie
AU - Phua, Min Wee
AU - Chong, Wei Binh
AU - Ang, Wei Tech
AU - Chua, Karen Sui Geok
N1 - Publisher Copyright:
Copyright © 2024 Pan, Sidarta, Wu, Kwong, Ong, Tay, Phua, Chong, Ang and Chua.
PY - 2024/7/22
Y1 - 2024/7/22
N2 - Background: This study aimed to identify and quantify the kinematic and kinetic gait deviations in post-stroke hemiplegic patients with matched healthy controls using Statistical Parametric Mapping (SPM). Methods: Fifteen chronic stroke patients [4 females, 11 males; age 53.7 (standard deviation 12.2) years; body mass 65.4 (10.4) kg; standing height 168.5 (9.6) cm] and 15 matched healthy controls [4 females, 11 males; age 52.9 (11.7) years; body weight 66.5 (10.7) years; standing height 168.3 (8.8) cm] were recruited. In a 10-m walking task, joint angles, ground reaction forces (GRF), and joint moments were collected, analyzed, and compared using SPM for an entire gait cycle. Results: Generally, when comparing the stroke patients’ affected (hemiplegic) and less-affected (contralateral) limbs with the control group, SPM identified significant differences in the late stance phase and early swing phase in the joint angles and moments in bilateral limbs (all p < 0.005). In addition, the vertical and anteroposterior components of GRF were significantly different in various periods of the stance phase (all p < 0.005), while the mediolateral component showed no differences between the two groups. Conclusion: SPM was able to detect abnormal gait patterns in both the affected and less-affected limbs of stroke patients with significant differences when compared with matched controls. The findings draw attention to significant quantifiable gait deviations in the less-affected post-stroke limb with the potential impact to inform gait retraining strategies for clinicians and physiotherapists.
AB - Background: This study aimed to identify and quantify the kinematic and kinetic gait deviations in post-stroke hemiplegic patients with matched healthy controls using Statistical Parametric Mapping (SPM). Methods: Fifteen chronic stroke patients [4 females, 11 males; age 53.7 (standard deviation 12.2) years; body mass 65.4 (10.4) kg; standing height 168.5 (9.6) cm] and 15 matched healthy controls [4 females, 11 males; age 52.9 (11.7) years; body weight 66.5 (10.7) years; standing height 168.3 (8.8) cm] were recruited. In a 10-m walking task, joint angles, ground reaction forces (GRF), and joint moments were collected, analyzed, and compared using SPM for an entire gait cycle. Results: Generally, when comparing the stroke patients’ affected (hemiplegic) and less-affected (contralateral) limbs with the control group, SPM identified significant differences in the late stance phase and early swing phase in the joint angles and moments in bilateral limbs (all p < 0.005). In addition, the vertical and anteroposterior components of GRF were significantly different in various periods of the stance phase (all p < 0.005), while the mediolateral component showed no differences between the two groups. Conclusion: SPM was able to detect abnormal gait patterns in both the affected and less-affected limbs of stroke patients with significant differences when compared with matched controls. The findings draw attention to significant quantifiable gait deviations in the less-affected post-stroke limb with the potential impact to inform gait retraining strategies for clinicians and physiotherapists.
KW - biomechanics
KW - gait analysis
KW - hemiplegia
KW - kinematic
KW - kinetic
KW - mobility
KW - Statistical Parametric Mapping
UR - http://www.scopus.com/inward/record.url?scp=85200261608&partnerID=8YFLogxK
U2 - 10.3389/fnins.2024.1425183
DO - 10.3389/fnins.2024.1425183
M3 - Journal article
AN - SCOPUS:85200261608
SN - 1662-4548
VL - 18
JO - Frontiers in Neuroscience
JF - Frontiers in Neuroscience
M1 - 1425183
ER -