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Upper limb strength training in subacute stroke patients: study protocol of a randomised controlled trial
BACKGROUND: Stroke patients are often affected by arm paresis, have functional impairments and receive help from professional or informal caregivers. Progressive resistance training is a common intervention for functional impairments after paresis. Randomised controlled trials (RCT) showed benefits...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6420769/ https://www.ncbi.nlm.nih.gov/pubmed/30876438 http://dx.doi.org/10.1186/s13063-019-3261-3 |
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author | Högg, Susan Holzgraefe, Manfred Wingendorf, Insa Mehrholz, Jan Herrmann, Christoph Obermann, Mark |
author_facet | Högg, Susan Holzgraefe, Manfred Wingendorf, Insa Mehrholz, Jan Herrmann, Christoph Obermann, Mark |
author_sort | Högg, Susan |
collection | PubMed |
description | BACKGROUND: Stroke patients are often affected by arm paresis, have functional impairments and receive help from professional or informal caregivers. Progressive resistance training is a common intervention for functional impairments after paresis. Randomised controlled trials (RCT) showed benefits for functional recovery after resistance training. However, there is a lack of evidence for strength training in subacute stroke patients. The aim of this study is to investigate safety and effectiveness of arm strength training in subacute stroke patients. METHODS: We will conduct a prospective, assessor-blinded RCT of people with subacute stroke. We will randomly assign patients to one of two parallel groups in a 1:1 ratio and will use concealed allocation. The intervention group will receive, in addition to standard treatment, high-intensity arm training (three times per week, over three weeks; 60 min each session; with a total of nine additional sessions). The control group will receive, in addition to standard treatment, low-intensity arm training (same quantity, frequency and treatment time as the intervention group). Standard treatment for the affected arm includes mobilisation, stretching, therapeutic positioning, arm and hand motor training, strengthening exercises, mechanical assisted training, functional training and task-oriented training. The primary efficacy endpoint will be grip strength. Secondary outcome measures will be Modified Ashworth Scale, Motricity Index, Fugl-Meyer Assessment for the upper limb, Box and Block Test and Goal Attainment Scale for individual participatory goals. We will measure primary and secondary outcomes with blinded assessors at baseline and immediately after three weeks of additional therapy. Based on our sample size calculation, 78 patients will be recruited from our rehabilitation hospital in two and a half years. Drop-out rates and adverse events will be systematically recorded. DISCUSSION: This study attempts to close the evidence gap for effects of arm strength training in subacute stroke patients. The results of this trial will provide robust evidence for effects and safety of high-intensity arm training for people with stroke. TRIAL REGISTRATION: German Clinical Trials Register, DRKS00012484. Registered on 26 May 2017. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13063-019-3261-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6420769 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-64207692019-03-28 Upper limb strength training in subacute stroke patients: study protocol of a randomised controlled trial Högg, Susan Holzgraefe, Manfred Wingendorf, Insa Mehrholz, Jan Herrmann, Christoph Obermann, Mark Trials Study Protocol BACKGROUND: Stroke patients are often affected by arm paresis, have functional impairments and receive help from professional or informal caregivers. Progressive resistance training is a common intervention for functional impairments after paresis. Randomised controlled trials (RCT) showed benefits for functional recovery after resistance training. However, there is a lack of evidence for strength training in subacute stroke patients. The aim of this study is to investigate safety and effectiveness of arm strength training in subacute stroke patients. METHODS: We will conduct a prospective, assessor-blinded RCT of people with subacute stroke. We will randomly assign patients to one of two parallel groups in a 1:1 ratio and will use concealed allocation. The intervention group will receive, in addition to standard treatment, high-intensity arm training (three times per week, over three weeks; 60 min each session; with a total of nine additional sessions). The control group will receive, in addition to standard treatment, low-intensity arm training (same quantity, frequency and treatment time as the intervention group). Standard treatment for the affected arm includes mobilisation, stretching, therapeutic positioning, arm and hand motor training, strengthening exercises, mechanical assisted training, functional training and task-oriented training. The primary efficacy endpoint will be grip strength. Secondary outcome measures will be Modified Ashworth Scale, Motricity Index, Fugl-Meyer Assessment for the upper limb, Box and Block Test and Goal Attainment Scale for individual participatory goals. We will measure primary and secondary outcomes with blinded assessors at baseline and immediately after three weeks of additional therapy. Based on our sample size calculation, 78 patients will be recruited from our rehabilitation hospital in two and a half years. Drop-out rates and adverse events will be systematically recorded. DISCUSSION: This study attempts to close the evidence gap for effects of arm strength training in subacute stroke patients. The results of this trial will provide robust evidence for effects and safety of high-intensity arm training for people with stroke. TRIAL REGISTRATION: German Clinical Trials Register, DRKS00012484. Registered on 26 May 2017. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13063-019-3261-3) contains supplementary material, which is available to authorized users. BioMed Central 2019-03-15 /pmc/articles/PMC6420769/ /pubmed/30876438 http://dx.doi.org/10.1186/s13063-019-3261-3 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Study Protocol Högg, Susan Holzgraefe, Manfred Wingendorf, Insa Mehrholz, Jan Herrmann, Christoph Obermann, Mark Upper limb strength training in subacute stroke patients: study protocol of a randomised controlled trial |
title | Upper limb strength training in subacute stroke patients: study protocol of a randomised controlled trial |
title_full | Upper limb strength training in subacute stroke patients: study protocol of a randomised controlled trial |
title_fullStr | Upper limb strength training in subacute stroke patients: study protocol of a randomised controlled trial |
title_full_unstemmed | Upper limb strength training in subacute stroke patients: study protocol of a randomised controlled trial |
title_short | Upper limb strength training in subacute stroke patients: study protocol of a randomised controlled trial |
title_sort | upper limb strength training in subacute stroke patients: study protocol of a randomised controlled trial |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6420769/ https://www.ncbi.nlm.nih.gov/pubmed/30876438 http://dx.doi.org/10.1186/s13063-019-3261-3 |
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