Following a stroke, both accumulating scientific evidence and medical guidelines recommend that patients receive high-dose neurorehabilitation to aid in recovery. The reality, however, is that most patients receive a fraction of the dose required. This gap between required and actual dose is due to implementational barriers, with lack of therapist availability and costs of high-dose delivery arguably being the two main ones. Here, we investigated the extent to which these barriers could be alleviated by using gamified self-training technologies at home under remote therapist supervision. We delivered a comprehensive full-body, high-dose neurorehabilitation program to chronic stroke patients entirely at home. The goal was to achieve approximately 36 hours of Active Training Time (ATT) over 12-18 weeks. The program was designed to be resource efficient, relying mostly on the patient training on their own (asynchronously) with the MindMotion GO gamified therapy solution. Additional telerehabilitation (synchronous) sessions with a therapist were interspersed once weekly, during which therapists used teleconference technologies to deliver additional training and provide direct feedback. Throughout, therapists were able to use a web application to continuously monitor and manage the training program remotely. We assessed effectiveness through reporting ATT, a measure more closely reflecting delivered dosage as opposed to scheduled dose. Patient recovery was evaluated with standardized impairment and functional clinical measures, and patient self-reported outcome measures. Finally, a cost model was computed to evaluate the resource efficiency of the program. Data from 17 patients was included in this retrospective analysis of a real-world clinical service. Patients completed an average cumulative ATT dose of 39.7 ±21.4 hours and maintained high levels of training adherence over the course of 19.2 ±3.3 weeks. The majority of the total ATT was delivered asynchronously (82.2 ±10.8% of total ATT). Patients showed improvements in both upper-limb (Fugl-Meyer Upper Extremity, 6.4 ±5.1 points; p<0.01) and gait and balance measures (Functional Gait Assessment, 3.1 ±2.6 points; p<0.01; Berg Balance Scale, 6.1 ±4.4 points; p<0.01). Overall, the program was viewed very favorably amongst patients, with 73.7% respondents being satisfied or very satisfied, while 63.2% of respondents reporting subjective improvements in physical abilities. Finally, therapist costs associated with the program amounted to $338 USD, thus representing a resource efficient alternative to delivering the same dose via one-on-one in-person training sessions (therapist costs amounting to $1903 USD). This work demonstrates that effective high-dose neurorehabilitation can be delivered via gamified therapy technologies in the home setting. Furthermore, we show that training time can be successfully decoupled from therapist-presence without compromising therapy delivery and outcomes or patient satisfaction. In the context of a growing concern over therapist availability worldwide, this program presents a human resource-efficient model that delivers high-dose neurorehabilitation as mandated by recent medical guidelines, complementing existing clinic-based approaches.
Competing Interest StatementAll authors have completed an ICMJE uniform disclosure form. SAA is an independent researcher contracted by MindMaze; DP, JTM, and GR have a research service agreement with MindMaze; MCC, AEF, and LTD are employed by MindMaze; DP and JTM are board members of Precision Recovery Inc; All other authors declare no other relationships or activities that could appear to have influenced this work.
Funding StatementThis study was funded by MindMaze
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:
Mount Sinai Program for the Protection of Human Subjects institutional review board of Icahn School of Medicine at Mount Sinai, New York, U.S.A. gave ethical approval for this work (STUDY-23-00276).
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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 AvailabilityAggregated and de-identified data that support the findings of this study are available from the corresponding authors upon reasonable request.
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