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

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 b...

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Autores principales: Turton, Ailie J, Cunningham, Paul, Heron, Emma, van Wijck, Frederike, Sackley, Cath, Rogers, Chris, Wheatley, Keith, Jowett, Sue, Wolf, Steven L, van Vliet, Paulette
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3675391/
https://www.ncbi.nlm.nih.gov/pubmed/23782653
http://dx.doi.org/10.1186/1745-6215-14-109
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author Turton, Ailie J
Cunningham, Paul
Heron, Emma
van Wijck, Frederike
Sackley, Cath
Rogers, Chris
Wheatley, Keith
Jowett, Sue
Wolf, Steven L
van Vliet, Paulette
author_facet Turton, Ailie J
Cunningham, Paul
Heron, Emma
van Wijck, Frederike
Sackley, Cath
Rogers, Chris
Wheatley, Keith
Jowett, Sue
Wolf, Steven L
van Vliet, Paulette
author_sort Turton, Ailie J
collection PubMed
description 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. TRIAL REGISTRATION: ISRCTN: ISRCTN56716589
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spelling pubmed-36753912013-06-08 Home-based reach-to-grasp training for people after stroke: study protocol for a feasibility randomized controlled trial Turton, Ailie J Cunningham, Paul Heron, Emma van Wijck, Frederike Sackley, Cath Rogers, Chris Wheatley, Keith Jowett, Sue Wolf, Steven L van Vliet, Paulette Trials Study Protocol 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. TRIAL REGISTRATION: ISRCTN: ISRCTN56716589 BioMed Central 2013-04-25 /pmc/articles/PMC3675391/ /pubmed/23782653 http://dx.doi.org/10.1186/1745-6215-14-109 Text en Copyright © 2013 Turton et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Study Protocol
Turton, Ailie J
Cunningham, Paul
Heron, Emma
van Wijck, Frederike
Sackley, Cath
Rogers, Chris
Wheatley, Keith
Jowett, Sue
Wolf, Steven L
van Vliet, Paulette
Home-based reach-to-grasp training for people after stroke: study protocol for a feasibility randomized controlled trial
title Home-based reach-to-grasp training for people after stroke: study protocol for a feasibility randomized controlled trial
title_full Home-based reach-to-grasp training for people after stroke: study protocol for a feasibility randomized controlled trial
title_fullStr Home-based reach-to-grasp training for people after stroke: study protocol for a feasibility randomized controlled trial
title_full_unstemmed Home-based reach-to-grasp training for people after stroke: study protocol for a feasibility randomized controlled trial
title_short Home-based reach-to-grasp training for people after stroke: study protocol for a feasibility randomized controlled trial
title_sort home-based reach-to-grasp training for people after stroke: study protocol for a feasibility randomized controlled trial
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3675391/
https://www.ncbi.nlm.nih.gov/pubmed/23782653
http://dx.doi.org/10.1186/1745-6215-14-109
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