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Author Notes:

Correspondence: Ailie J Turton, Department of Allied Health Professions, University of the West of England, Bristol, BS351NS, UK; Email: ailie.turton@uwe.ac.uk

Authors’ contributions: Intellectual contributions were made by CR, PC and EH.

All authors contributed to the development and writing of the protocol to its final version.

All authors have been involved in the drafting and revision of this manuscript, and have given approval of the final manuscript.

Acknowledgments: We thank the Stroke Research Network Officers (Sarah Hierons, Sarah Dunn and Amy Steele); the principal investigators (Colin Domaille, Becky Woodward, Chris Easton, Rhiannon Ferguson-Thomas and Fiona Henchie), and the local collaborators (Bryony Williams, Martin Boyd and Martine Stanhope), for their contribution to discussions about logistics of procedures for screening and recruitment, and for their support in facilitating training of clinicians in the study procedures.

Disclosures: The authors declare that they have no competing interests.

Subject:

Research Funding:

This study is supported by the Stroke Association (TSA 2009/01).

AT, FvW, CS, KW, SJ, SW, PvV are grant holders.

Keywords:

  • Stroke
  • Hand
  • Arm
  • Physical therapy
  • Occupational therapy
  • Rehabilitation
  • Home
  • Reach
  • Grasp
  • Task-specific training

Home-based reach-to-grasp training for people after stroke: study protocol for a feasibility randomized controlled trial

Journal Title:

Trials

Volume:

Volume 14, Number 109

Publisher:

, Pages 1-10

Type of Work:

Article | Final Publisher PDF

Abstract:

Background This feasibility study is intended to assess the acceptability of home-based task-specific reach-to-grasp (RTG) training for people with stroke, and to gather data to inform recruitment, retention, and sample size for a definitive randomized controlled trial. Methods/design This is to be a randomized controlled feasibility trial recruiting 50 individuals with upper-limb motor impairment after stroke. Participants will be recruited after discharge from hospital and up to 12 months post-stroke from hospital stroke services and community therapy-provider services. Participants will be assessed at baseline, and then electronically randomized and allocated to group by minimization, based on the time post-stroke and extent of upper-limb impairment. The intervention group will receive 14 training sessions, each 1 hour long, with a physiotherapist over 6 weeks and will be encouraged to practice independently for 1 hour/day to give a total of 56 hours of training time per participant. Participants allocated to the control group will receive arm therapy in accordance with usual care. Participants will be measured at 7 weeks post-randomization, and followed-up at 3 and 6 months post-randomization. Primary outcome measures for assessment of arm function are the Action Research Arm Test (ARAT) and Wolf Motor Function Test (WMFT). Secondary measures are the Motor Activity Log, Stroke Impact Scale, Carer Strain Index, and health and social care resource use. All assessments will be conducted by a trained assessor blinded to treatment allocation. Recruitment, adherence, withdrawals, adverse events (AEs), and completeness of data will be recorded and reported. Discussion This study will determine the acceptability of the intervention, the characteristics of the population recruited, recruitment and retention rates, descriptive statistics of outcomes, and incidence of AEs. It will provide the information needed for planning a definitive trial to test home-based RTG training.

Copyright information:

© 2013 Turton et al.; licensee BioMed Central Ltd.

This is an Open Access work distributed under the terms of the Creative Commons Attribution 2.0 Generic License (http://creativecommons.org/licenses/by/2.0/).

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