2023
DOI: 10.1177/15459683231174223
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Autonomous Control of Music to Retrain Walking After Stroke

Abstract: Background Post-stroke care guidelines highlight continued rehabilitation as essential; however, many stroke survivors cannot participate in outpatient rehabilitation. Technological advances in wearable sensing, treatment algorithms, and care delivery interfaces have created new opportunities for high-efficacy rehabilitation interventions to be delivered autonomously in any setting (ie, clinic, community, or home). Methods We developed an autonomous rehabilitation system that combines the closed-loop control o… Show more

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Cited by 6 publications
(1 citation statement)
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References 77 publications
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“…These strengths add to the compounding evidence for InTandem to be used by the intended population in the intended environment for use. The accumulated evidence for InTandem includes a feasibility study that resulted in clinically relevant improvements in speed over 1 and multiple sessions [ 30 ] and a reduction in the energetic cost of walking along with improved gait asymmetries [ 31 ]; a longitudinal RCT of safety and clinical efficacy of InTandem [ 32 ]; and a budget impact model that estimates cost savings to payers [ 33 ]. Furthermore, MR-001 (InTandem) was designated as a breakthrough device by the FDA in 2020 [ 34 ], which underscores both the unmet need to address persistent walking deficits of people who are in the chronic stroke phase of recovery in an accessible and effective manner and the merit and opportunity that InTandem offers them.…”
Section: Discussionmentioning
confidence: 99%
“…These strengths add to the compounding evidence for InTandem to be used by the intended population in the intended environment for use. The accumulated evidence for InTandem includes a feasibility study that resulted in clinically relevant improvements in speed over 1 and multiple sessions [ 30 ] and a reduction in the energetic cost of walking along with improved gait asymmetries [ 31 ]; a longitudinal RCT of safety and clinical efficacy of InTandem [ 32 ]; and a budget impact model that estimates cost savings to payers [ 33 ]. Furthermore, MR-001 (InTandem) was designated as a breakthrough device by the FDA in 2020 [ 34 ], which underscores both the unmet need to address persistent walking deficits of people who are in the chronic stroke phase of recovery in an accessible and effective manner and the merit and opportunity that InTandem offers them.…”
Section: Discussionmentioning
confidence: 99%