Walking, a seemingly simple task for many, becomes a challenge for people after a stroke. Typically, the swinging leg kinematics is fine-tuned to provide toe clearance, but reduced knee flexion after stroke requires adaptive gait strategies, such as hip hiking and circumduction, to prevent stumbling. The cause of reduced knee flexion in a dynamic system is unintuitive and often obscured by muscle weakness, hyperactivity, or abnormal joint coordination. Using physical models, we predicted that intersegmental forces may be largely responsible for the deficits. Leveraging subject-specific inverse modeling of body dynamics, we compared force generation in post-stroke and neurotypical participants in overground walking. We tested if the contribution of active muscle-generated and passive intersegmental torques from neighboring segments may be responsible for the observed reduced knee flexion. The similar levels of active knee torque across both study groups at the onset of swing indicated that knee interaction torque is the main cause; the component of this torque generated at the hip was decreased (more than that at the ankle) in the post-stroke group. Identified deficit in hip flexion torque at swing onset unveils a key biomechanical mechanism underlying reduced knee flexion post-stroke, providing a physics-informed target for post-stroke gait rehabilitation.
Competing Interest StatementThe authors have declared no competing interest.
Funding StatementThis study was funded by the NIH Award 1 R03 HD099426-01A1 and the Sao Paulo State Research Foundation (FAPESP) Grant 2018/04964-8. Additional support was provided by the West Virginia University Center for Foundational Neuroscience Research and Education, the West Virginia University Stroke and Its Alzheimers Disease Related Dementias (ADRD) T32 Program, the West Virginia Foundation Distinguished Doctoral Scholarship Program, the Mitochondria, Metabolism & Bioenergetics (MMB) Working Group, and the Community Foundation for the Ohio Valley Whipkey Trust.
Author DeclarationsI confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.
Yes
The details of the IRB/oversight body that provided approval or exemption for the research described are given below:
Ethics committee of Cruzeiro do Sul University gave ethical approval for this work (ethical review committee CAAE 02887518.2.0000.8084).
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Yes
I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).
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I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.
Yes
Data AvailabilityAll data produced in the present study are available upon reasonable request to the authors.
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