Abstract
Acquiring gait parameters from usual walking is important to predict clinical outcomes, including life expectancy, risk of fall, and neurocognitive performance, in older people. For comprehensive gait analysis, instruments such as marker-based motion analysis systems and walkways with pressure sensor arrays are necessary. Traditional instruments are bulky, complex, expensive, and intrinsically intrusive. Requirements of dedicated spaces for installation and specialized staff make it difficult to utilize traditional gait analysis instruments in most outpatient clinics. We present a novel gait analysis tool that is small, highly accurate, easy-to-use, and non-intrusive and is based on two-dimensional light detection and ranging technology. Using an object-tracking algorithm, we conducted a validation study of spatiotemporal tracking of ankle locations of subjects by comparing our tool with a gold standard modality. Our tool showed successful acquisition of gait parameters from usual walking motions and trackability with multiple targets in noisy conditions, including typical clinical environments.
Competing Interest Statement
S.Y, H.W.J, and H.R cofounded Dyphi Inc.
Clinical Trial
This study was not a clinical trial
Funding Statement
This study was supported by grant No.0420202070 from the Seoul National University Hospital Research Fund.
Author Declarations
I 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:
The institutional review board of National Traffic Injury Rehabilitation Hospital approved the study protocol (No. NTRH-20004), and written informed consent was acquired from all participants.
All necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived.
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).
Yes
I have followed all appropriate research reporting guidelines and uploaded the relevant EQUATOR Network research reporting checklist(s) and other pertinent material as supplementary files, if applicable.
Yes
Data Availability
The datasets generated during the current study are available from the corresponding authors upon reasonable request.