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Cover of Robot-assisted training compared with an enhanced upper limb therapy programme and with usual care for upper limb functional limitation after stroke: the RATULS three-group RCT

Robot-assisted training compared with an enhanced upper limb therapy programme and with usual care for upper limb functional limitation after stroke: the RATULS three-group RCT

Health Technology Assessment, No. 24.54

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Author Information and Affiliations
Southampton (UK): NIHR Journals Library; .

Headline

Robot-assisted training did not improve upper limb function after stroke when compared with an enhanced upper limb therapy programme, or usual care.

Abstract

Background:

Loss of arm function is common after stroke. Robot-assisted training may improve arm outcomes.

Objective:

The objectives were to determine the clinical effectiveness and cost-effectiveness of robot-assisted training, compared with an enhanced upper limb therapy programme and with usual care.

Design:

This was a pragmatic, observer-blind, multicentre randomised controlled trial with embedded health economic and process evaluations.

Setting:

The trial was set in four NHS trial centres.

Participants:

Patients with moderate or severe upper limb functional limitation, between 1 week and 5 years following first stroke, were recruited.

Interventions:

Robot-assisted training using the Massachusetts Institute of Technology-Manus robotic gym system (InMotion commercial version, Interactive Motion Technologies, Inc., Watertown, MA, USA), an enhanced upper limb therapy programme comprising repetitive functional task practice, and usual care.

Main outcome measures:

The primary outcome was upper limb functional recovery ‘success’ (assessed using the Action Research Arm Test) at 3 months. Secondary outcomes at 3 and 6 months were the Action Research Arm Test results, upper limb impairment (measured using the Fugl-Meyer Assessment), activities of daily living (measured using the Barthel Activities of Daily Living Index), quality of life (measured using the Stroke Impact Scale), resource use costs and quality-adjusted life-years.

Results:

A total of 770 participants were randomised (robot-assisted training, n = 257; enhanced upper limb therapy, n = 259; usual care, n = 254). Upper limb functional recovery ‘success’ was achieved in the robot-assisted training [103/232 (44%)], enhanced upper limb therapy [118/234 (50%)] and usual care groups [85/203 (42%)]. These differences were not statistically significant; the adjusted odds ratios were as follows: robot-assisted training versus usual care, 1.2 (98.33% confidence interval 0.7 to 2.0); enhanced upper limb therapy versus usual care, 1.5 (98.33% confidence interval 0.9 to 2.5); and robot-assisted training versus enhanced upper limb therapy, 0.8 (98.33% confidence interval 0.5 to 1.3). The robot-assisted training group had less upper limb impairment (as measured by the Fugl-Meyer Assessment motor subscale) than the usual care group at 3 and 6 months. The enhanced upper limb therapy group had less upper limb impairment (as measured by the Fugl-Meyer Assessment motor subscale), better mobility (as measured by the Stroke Impact Scale mobility domain) and better performance in activities of daily living (as measured by the Stroke Impact Scale activities of daily living domain) than the usual care group, at 3 months. The robot-assisted training group performed less well in activities of daily living (as measured by the Stroke Impact Scale activities of daily living domain) than the enhanced upper limb therapy group at 3 months. No other differences were clinically important and statistically significant. Participants found the robot-assisted training and the enhanced upper limb therapy group programmes acceptable. Neither intervention, as provided in this trial, was cost-effective at current National Institute for Health and Care Excellence willingness-to-pay thresholds for a quality-adjusted life-year.

Conclusions:

Robot-assisted training did not improve upper limb function compared with usual care. Although robot-assisted training improved upper limb impairment, this did not translate into improvements in other outcomes. Enhanced upper limb therapy resulted in potentially important improvements on upper limb impairment, in performance of activities of daily living, and in mobility. Neither intervention was cost-effective.

Future work:

Further research is needed to find ways to translate the improvements in upper limb impairment seen with robot-assisted training into improvements in upper limb function and activities of daily living. Innovations to make rehabilitation programmes more cost-effective are required.

Limitations:

Pragmatic inclusion criteria led to the recruitment of some participants with little prospect of recovery. The attrition rate was higher in the usual care group than in the robot-assisted training or enhanced upper limb therapy groups, and differential attrition is a potential source of bias. Obtaining accurate information about the usual care that participants were receiving was a challenge.

Trial registration:

Current Controlled Trials ISRCTN69371850.

Funding:

This project was funded by the National Institute for Health Research (NIHR) Health Technology Assessment programme and will be published in full in Health Technology Assessment; Vol. 24, No. 54. See the NIHR Journals Library website for further project information.

Contents

About the Series

Health Technology Assessment
ISSN (Print): 1366-5278
ISSN (Electronic): 2046-4924

Declared competing interests of authors: Helen Rodgers reports personal fees from Bayer AG (Leverkusen, Germany) outside the submitted work and was a member of the National Institute for Health Research (NIHR) Health Technology Assessment (HTA) Clinical Evaluations and Trials (CET) panel (2010–14). Gary A Ford reports personal fees from Amgen Inc. (Thousand Oaks, CA, USA), Bayer AG, Stryker Corporation (Kalamazoo, MI, USA) and Pfizer Inc. (New York, NY, USA), and grants and personal fees from Medtronic plc (Dublin, Ireland), outside the submitted work. Hermano I Krebs reports other financial activity from Interactive Motion Technologies Inc. (Boston, MA, USA) and 4Motion Robotics (Waterton, MA, USA) outside the submitted work. In addition, he has a patent issued (Interactive Robotic Therapist; US Patent 5,466,213; 1995; Massachusetts Institute of Technology) and a patent (Wrist And Upper Extremity Motion; US Patent No. 7,618,381; 2009; Massachusetts Institute of Technology) licensed to Bionik Laboratories Corp. (Toronto, ON, Canada). Denise Howel reports membership of the NIHR Programme Grants for Applied Research Programme subcommittee (2016 to present), and was a member of the NIHR Health Services and Delivery Research Programme Commissioning Board (2012–15). Jesse Dawson reports other financial activity from MicroTransponder Inc. (Austin, TX, USA) outside the submitted work. Luke Vale was a member of the NIHR HTA CET panel (2015–18).

Article history

The research reported in this issue of the journal was funded by the HTA programme as project number 11/26/05. The contractual start date was in January 2014. The draft report began editorial review in December 2019 and was accepted for publication in May 2020. The authors have been wholly responsible for all data collection, analysis and interpretation, and for writing up their work. The HTA editors and publisher have tried to ensure the accuracy of the authors’ report and would like to thank the reviewers for their constructive comments on the draft document. However, they do not accept liability for damages or losses arising from material published in this report.

Last reviewed: December 2019; Accepted: May 2020.

Joint first authorship

Copyright © Queen’s Printer and Controller of HMSO 2020. This work was produced by Rodgers et al. under the terms of a commissioning contract issued by the Secretary of State for Health and Social Care. This issue may be freely reproduced for the purposes of private research and study and extracts (or indeed, the full report) may be included in professional journals provided that suitable acknowledgement is made and the reproduction is not associated with any form of advertising. Applications for commercial reproduction should be addressed to: NIHR Journals Library, National Institute for Health Research, Evaluation, Trials and Studies Coordinating Centre, Alpha House, University of Southampton Science Park, Southampton SO16 7NS, UK.
Bookshelf ID: NBK563647DOI: 10.3310/hta24540

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