Optimized Home Rehabilitation Technology Reduces Upper Extremity Impairment Compared to a Conventional Home Exercise Program: A Randomized, Controlled, Single-Blind Trial in Subacute Stroke

Author:

Swanson Veronica A.1ORCID,Johnson Christopher2,Zondervan Daniel K.3,Bayus Nicole4,McCoy Phylicia5,Ng Yat Fung Joshua6,Schindele, BS Jenna7,Reinkensmeyer David J.18,Shaw Susan9

Affiliation:

1. Department of Mechanical and Aerospace Engineering, Henry Samueli School of Engineering, University of California, Irvine, Irvine, CA, USA

2. Department of Biomedical Engineering, Henry Samueli School of Engineering, University of California, Irvine, Irvine, CA, USA

3. Flint Rehabilitation Devices, LLC, Irvine, CA, USA

4. Rancho Research Institute, Rancho Los Amigos National Rehabilitation Hospital, Downey, USA

5. Arthur J. Bond Department of Mechanical Engineering, Alabama A&M University, Huntsville, AL, USA

6. School of Social Sciences, University of California, Irvine, Irvine, CA, USA

7. Mathematics and Statistics, University of California, Los Angeles, Los Angeles, CA, USA

8. Department of Anatomy and Neurobiology, UC Irvine School of Medicine, University of California, Irvine, Irvine, CA, USA

9. Department of Neurology, Rancho Los Amigos National Rehabilitation Center, Downey, CA, USA

Abstract

Background Upper extremity (UE) stroke rehabilitation requires patients to perform exercises at home, yet patients show limited benefit from paper-based home exercise programs. Objective To compare the effectiveness of 2 home exercise programs for reducing UE impairment: a paper-based approach and a sensorized exercise system that incorporates recommended design features for home rehabilitation technology. Methods In this single-blind, randomized controlled trial, 27 participants in the subacute phase of stroke were assigned to the sensorized exercise (n = 14) or conventional therapy group (n = 13), though 2 participants in the conventional therapy group were lost to follow-up. Participants were instructed to perform self-guided movement training at home for at least 3 hours/week for 3 consecutive weeks. The sensorized exercise group used FitMi, a computer game with 2 puck-like sensors that encourages movement intensity and auto-progresses users through 40 exercises. The conventional group used a paper book of exercises. The primary outcome measure was the change in Upper Extremity Fugl–Meyer (UEFM) score from baseline to follow-up. Secondary measures included the Modified Ashworth Scale for spasticity (MAS) and the Visual Analog Pain (VAP) scale. Results Participants who used FitMi improved by an average of 8.0 ± 4.6 points on the UEFM scale compared to 3.0 ± 6.1 points for the conventional participants, a significant difference ( t-test, P = .029). FitMi participants exhibited no significant changes in UE MAS or VAP scores. Conclusions A sensor-based exercise system incorporating a suite of recommended design features significantly and safely reduced UE impairment compared to a paper-based, home exercise program. Trial Registration: ClinicalTrials.gov Identifier: NCT03503617

Funder

National Institute on Aging

National Institute of Independent Living, Disability, and Rehabilitation Research

Publisher

SAGE Publications

Subject

General Medicine

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