期刊
JOURNAL OF NEUROENGINEERING AND REHABILITATION
卷 20, 期 1, 页码 -出版社
BMC
DOI: 10.1186/s12984-023-01243-3
关键词
Stroke; Gait; Lokomat (R); Inpatient Rehabilitation Facility
This study aimed to investigate the feasibility of early and intense supplemental gait training during inpatient stroke rehabilitation and compare the functional outcomes between different training methods. The results showed that supplemental therapy could be implemented without interrupting schedules and participants achieved meaningful functional improvement in a relatively short time.
Introduction: Practicality of implementation and dosing of supplemental gait training in an acute stroke inpatient rehabilitation setting are not well studied but can have positive impact on outcomes.Objectives: To determine the feasibility of early, intense supplemental gait training in inpatient stroke rehabilitation, compare functional outcomes and the specific mode of delivery.Design and setting: Assessor blinded, randomized controlled trial in a tertiary Inpatient Rehabilitation Facility.Participants: Thirty acute post-stroke patients with unilateral hemiparesis (>= 18 years of age with a lower limb MAS <= 3).Intervention: Lokomat (R) or conventional gait training (CGT) in addition to standard mandated therapy time.Main outcome measures: Number of therapy sessions; adverse events; functional independence measure (FIM motor); functional ambulation category (FAC); passive range of motion (PROM); modified Ashworth scale (MAS); 5 times sit-to-stand (5x-STS); 10-m walk test (10MWT); 2-min walk test (2MWT) were assessed before (pre) and after training (post).Results: The desired supplemental therapy was implemented during normal care delivery hours and the patients generally tolerated the sessions well. Both groups improved markedly on several measures; the CGT group obtained nearly 45% more supplemental sessions (12.8) than the Lokomat (R) group (8.9). Both groups showed greater FIM improvement scores (discharge - admission) than those from a reference group receiving no supplemental therapy. An overarching statistical comparison between methods was skewed towards a differential benefit (but not significant) in the Lokomat (R) group with medium effect sizes. By observation, the robotic group completed a greater number of steps, on average. These results provide some evidence for Lokomat (R) being a more efficient tool for gait retraining by providing a more optimal therapy dose.Conclusions: With careful planning, supplemental therapy was possible with minimal intrusion to schedules and was well tolerated. Participants showed meaningful functional improvement with relatively little supplemental therapy over a relatively short time in study.
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