Biomechanics studies using traditional optical motion capture have been limited by small, homogeneous sample sizes and a focus on single movements, restricting the ability to capture clinically relevant adaptations across daily tasks. These limitations are particularly consequential in heterogeneous musculoskeletal conditions such as knee osteoarthritis (OA), where variability in demographic and clinical characteristics necessitates large, representative samples to identify patient-specific biomechanical intervention targets. Markerless motion capture enables faster, high-throughput data collection and offers the potential for community-based assessments; however, its feasibility of use in clinical populations across diverse tasks remains unclear. This study evaluated the feasibility of community-based, high-throughput markerless biomechanics data collection in individuals with knee OA. Participants (n = 85) completed a series of activities of daily living using a portable markerless motion capture system deployed across two community-based and two on-campus sites. Feasibility was assessed using timing metrics related to research operations (transit, setup, calibration, breakdown), participant workflow (consent, questionnaires, motion capture), and task-specific durations. No significant differences in timing metrics were observed across sites despite logistical and operational challenges. These findings support the feasibility of using high-throughput, community-based markerless motion capture and suggest a viable pathway for addressing long-standing limitations in sample size and representativeness through scalable data collection workflows in biomechanics studies.
Competing Interest StatementThe authors have declared no competing interest.
Funding StatementThis research was supported by a grant from the National Institute on Aging, Claude D. Pepper Older Americans Independence Center at the University of Florida (P30 AG028740). This project utilized REDCap, which is supported by the National Center for Advancing Translational Sciences of the National Institutes of Health (UL1TR001427). KEC was supported by an Investigator Award from the Rheumatology Research Foundation. RCM was supported by a Herbert Wertheim College of Engineering Deans Research Award from the University of Florida.
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:
The Institutional Review Board of the University of Florida gave ethical approval for this work
I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.
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, 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
Comments (0)