Objective: We examined the single-session feasibility of a wearable device to deliver a closed-loop music-based rhythmic auditory stimulation (RAS) walking intervention in people with knee osteoarthritis (OA). Methods: Fifteen participants with knee OA (age 70.0 (8.6) years; BMI 29.4(5.9) kg/m2; 10 women) complete a supervised 30-minute walking session using a wearable music-based RAS device. The device included shoe-worn inertial sensors, headphones, and a proprietary algorithm embedded in a touchscreen control unit. The algorithm continuously assessed the gait of the user and adjusted the tempo of the selected music to encourage improvements in gait quality. Spatiotemporal gait measures were collected using separate inertial sensors during the session. We examined change in gait during the session, report of exertion, and participant-reported acceptability. Results: On average, participants showed approximately 12%, 30%, and 15% increases in cadence, gait speed, and stride length, respectively without worsening variability or symmetry from before to during the RAS session. Of the 15 participants, 9/15, 11/15, and 9/15 showed at least 10% increase in cadence, gait speed, and stride length, respectively. Rating of Perceived Exertion was on average 13.3 (range 12-15). There were no serious adverse events and small increase in knee pain that resolved at the end of the session. Participants were highly accepting of the device and willing to use it at home for longer periods. Conclusion: A single-session feasibility study of a wearable closed-loop music-based RAS device in people with knee OA demonstrated increases in cadence and gait speed while safely walking at a moderate exercise intensity under supervision.
Competing Interest StatementDr. Kumar received funding for this work from MedRhythms, Inc. MedRhythms was not involved in study design, data analysis, data interpretation, or manuscript preparation. No MedRhythms employees or affiliates are authors on this work. Publication of this manuscript was not contingent upon approval from MedRhythms.
Funding StatementFunding for this study was provided by MedRhythms Inc. and Boston University Undergraduate Research Opportunities Program.
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:
IRB of Boston University gave ethical approval for this work.
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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.
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Data AvailabilityAll data produced in the present study are available upon reasonable request to the authors
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