Bilateral hip exoskeleton assistance enables faster walking in individuals with chronic stroke-related gait impairments
- PMID: 39814856
- PMCID: PMC11735669
- DOI: 10.1038/s41598-025-86343-x
Bilateral hip exoskeleton assistance enables faster walking in individuals with chronic stroke-related gait impairments
Abstract
Millions of individuals surviving a stroke have lifelong gait impairments that reduce their personal independence and quality of life. Reduced walking speed is one of the major problems limiting community mobility and reintegration. Previous studies have shown positive effect of robot-assisted gait training utilizing hip exoskeletons for individuals with gait impairments due to a stroke, leading to increased walking speed in post-treatment compared to pre-treatment assessments. However, no evidence emerged of a significant increasing in walking speed attributable to device usage compared to walking without the device. In this pilot investigation, we observed that hip flexion/extension assistance delivered by a portable bilateral powered hip exoskeleton increased overground self-selected walking speed by 20.2 ± 5.0% on average among six chronic post-stroke survivors. When comparing walking with and without the hip exoskeleton within the same experimental session, the observed speed increment resulted in statistically and clinically meaningful improvement (0.14 ± 0.03 m/s > minimal clinically important difference, p = 0.015). The increased walking speed was the result of a higher self-selected cadence and longer step length both on the paretic and nonparetic limbs. By facilitating gait, a bilateral hip exoskeleton could be a viable technology for extending locomotor mobility and facilitating gait training of individuals affected by post-stroke hemiparesis.
© 2025. The Author(s).
Conflict of interest statement
Ethics approval and consent to participate: The study was approved the local Ethics Committee, namely the Comitato Area Vasta Centro Toscana (Protocol ID: CLs + + 2ndCS; approval number: 16454_spe) and notified to the Italian Ministry of Health. All participants provided written informed consent. Competing interests: R.C., F.G., N.V., and S.C. have interests in IUVO S.r.l. (Pontedera, Pisa, Italy). The IP covering the technology presented in this paper has been exclusively licensed to IUVO. T.F. and A.A. are employed by Össur. A.E. is a member of the Össur Board. Össur is a shareholder of IUVO S.r.l. The other authors declare no competing interests.
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