Cargando…

Gothenburg very early supported discharge study (GOTVED) NCT01622205: a block randomized trial with superiority design of very early supported discharge for patients with stroke

BACKGROUND: Stroke is the disease with the highest costs for hospital care and also after discharge. Early supported discharge (ESD) has shown to be efficient and safe and the best results with well-organised discharge teams and patients with less severe strokes. The aim is to investigate if very ea...

Descripción completa

Detalles Bibliográficos
Autores principales: Sunnerhagen, Katharina S, Danielsson, Anna, Rafsten, Lena, Björkdahl, Ann, Axelsson, Åsa B, Nordin, Åsa, Petersson, Cathrine A, Lundgren-Nilsson, Åsa, Fröjd, Karin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3694454/
https://www.ncbi.nlm.nih.gov/pubmed/23800106
http://dx.doi.org/10.1186/1471-2377-13-66
_version_ 1782274858027057152
author Sunnerhagen, Katharina S
Danielsson, Anna
Rafsten, Lena
Björkdahl, Ann
Axelsson, Åsa B
Nordin, Åsa
Petersson, Cathrine A
Lundgren-Nilsson, Åsa
Fröjd, Karin
author_facet Sunnerhagen, Katharina S
Danielsson, Anna
Rafsten, Lena
Björkdahl, Ann
Axelsson, Åsa B
Nordin, Åsa
Petersson, Cathrine A
Lundgren-Nilsson, Åsa
Fröjd, Karin
author_sort Sunnerhagen, Katharina S
collection PubMed
description BACKGROUND: Stroke is the disease with the highest costs for hospital care and also after discharge. Early supported discharge (ESD) has shown to be efficient and safe and the best results with well-organised discharge teams and patients with less severe strokes. The aim is to investigate if very early supported discharge (VESD) for stroke patients in need for on-going individualised rehabilitation at home is useful for the patient and cost effective. METHODS/DESIGN: A randomized controlled trial comparing VESD with ordinary discharge. Inclusion criteria: confirmed stroke, >18 years of age, living within 30 min from the stroke unit, on day 2 0–16 points on the National institute of health stroke scale (NIHSS) and 50–100 points on the Barthel Index (BI), with BI 100 then the patient can be included if the Montreal Cognitive Assessment is < 26. Exclusion criteria are: NIHSS >16, BI < 50, life expectancy < 1 year, inability to speak or to communicate in Swedish. The inclusion occurs on day 4 and in block randomization of 20 and with blinded assessor. Primary outcome: levels of anxiety and depression. Secondary outcomes: independence, security, level of function, quality of health, needs of support in activities of daily living and caregiver burden. Power calculation is based on the level of anxiety and with a power of 80%, p-value 0.05 (2 sided test) 44 persons per group are needed. Data is gathered on co-morbidity, re-entry to hospital, mortality and a health economic analysis. Interviews will be accomplished with a strategic sample of 15 patients in the intervention group before discharge, within two weeks after homecoming and 3 months later. Interviews are also planned with 15 relatives in the intervention group 3 months after discharge. DISCUSSION: The ESD studies in the Cochrane review present hospital stays of a length that no longer exist in Sweden. There is not yet, to our knowledge, any study of early supported discharge with present length of hospital stay. Thus it is not clear if home rehabilitation nowadays without risks, is cost effective, or with the same patient usefulness as earlier studies. TRIAL REGISTRATION: ClinicalTrials.gov NCT01622205
format Online
Article
Text
id pubmed-3694454
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-36944542013-06-28 Gothenburg very early supported discharge study (GOTVED) NCT01622205: a block randomized trial with superiority design of very early supported discharge for patients with stroke Sunnerhagen, Katharina S Danielsson, Anna Rafsten, Lena Björkdahl, Ann Axelsson, Åsa B Nordin, Åsa Petersson, Cathrine A Lundgren-Nilsson, Åsa Fröjd, Karin BMC Neurol Study Protocol BACKGROUND: Stroke is the disease with the highest costs for hospital care and also after discharge. Early supported discharge (ESD) has shown to be efficient and safe and the best results with well-organised discharge teams and patients with less severe strokes. The aim is to investigate if very early supported discharge (VESD) for stroke patients in need for on-going individualised rehabilitation at home is useful for the patient and cost effective. METHODS/DESIGN: A randomized controlled trial comparing VESD with ordinary discharge. Inclusion criteria: confirmed stroke, >18 years of age, living within 30 min from the stroke unit, on day 2 0–16 points on the National institute of health stroke scale (NIHSS) and 50–100 points on the Barthel Index (BI), with BI 100 then the patient can be included if the Montreal Cognitive Assessment is < 26. Exclusion criteria are: NIHSS >16, BI < 50, life expectancy < 1 year, inability to speak or to communicate in Swedish. The inclusion occurs on day 4 and in block randomization of 20 and with blinded assessor. Primary outcome: levels of anxiety and depression. Secondary outcomes: independence, security, level of function, quality of health, needs of support in activities of daily living and caregiver burden. Power calculation is based on the level of anxiety and with a power of 80%, p-value 0.05 (2 sided test) 44 persons per group are needed. Data is gathered on co-morbidity, re-entry to hospital, mortality and a health economic analysis. Interviews will be accomplished with a strategic sample of 15 patients in the intervention group before discharge, within two weeks after homecoming and 3 months later. Interviews are also planned with 15 relatives in the intervention group 3 months after discharge. DISCUSSION: The ESD studies in the Cochrane review present hospital stays of a length that no longer exist in Sweden. There is not yet, to our knowledge, any study of early supported discharge with present length of hospital stay. Thus it is not clear if home rehabilitation nowadays without risks, is cost effective, or with the same patient usefulness as earlier studies. TRIAL REGISTRATION: ClinicalTrials.gov NCT01622205 BioMed Central 2013-06-24 /pmc/articles/PMC3694454/ /pubmed/23800106 http://dx.doi.org/10.1186/1471-2377-13-66 Text en Copyright © 2013 Sunnerhagen 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
Sunnerhagen, Katharina S
Danielsson, Anna
Rafsten, Lena
Björkdahl, Ann
Axelsson, Åsa B
Nordin, Åsa
Petersson, Cathrine A
Lundgren-Nilsson, Åsa
Fröjd, Karin
Gothenburg very early supported discharge study (GOTVED) NCT01622205: a block randomized trial with superiority design of very early supported discharge for patients with stroke
title Gothenburg very early supported discharge study (GOTVED) NCT01622205: a block randomized trial with superiority design of very early supported discharge for patients with stroke
title_full Gothenburg very early supported discharge study (GOTVED) NCT01622205: a block randomized trial with superiority design of very early supported discharge for patients with stroke
title_fullStr Gothenburg very early supported discharge study (GOTVED) NCT01622205: a block randomized trial with superiority design of very early supported discharge for patients with stroke
title_full_unstemmed Gothenburg very early supported discharge study (GOTVED) NCT01622205: a block randomized trial with superiority design of very early supported discharge for patients with stroke
title_short Gothenburg very early supported discharge study (GOTVED) NCT01622205: a block randomized trial with superiority design of very early supported discharge for patients with stroke
title_sort gothenburg very early supported discharge study (gotved) nct01622205: a block randomized trial with superiority design of very early supported discharge for patients with stroke
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3694454/
https://www.ncbi.nlm.nih.gov/pubmed/23800106
http://dx.doi.org/10.1186/1471-2377-13-66
work_keys_str_mv AT sunnerhagenkatharinas gothenburgveryearlysupporteddischargestudygotvednct01622205ablockrandomizedtrialwithsuperioritydesignofveryearlysupporteddischargeforpatientswithstroke
AT danielssonanna gothenburgveryearlysupporteddischargestudygotvednct01622205ablockrandomizedtrialwithsuperioritydesignofveryearlysupporteddischargeforpatientswithstroke
AT rafstenlena gothenburgveryearlysupporteddischargestudygotvednct01622205ablockrandomizedtrialwithsuperioritydesignofveryearlysupporteddischargeforpatientswithstroke
AT bjorkdahlann gothenburgveryearlysupporteddischargestudygotvednct01622205ablockrandomizedtrialwithsuperioritydesignofveryearlysupporteddischargeforpatientswithstroke
AT axelssonasab gothenburgveryearlysupporteddischargestudygotvednct01622205ablockrandomizedtrialwithsuperioritydesignofveryearlysupporteddischargeforpatientswithstroke
AT nordinasa gothenburgveryearlysupporteddischargestudygotvednct01622205ablockrandomizedtrialwithsuperioritydesignofveryearlysupporteddischargeforpatientswithstroke
AT peterssoncathrinea gothenburgveryearlysupporteddischargestudygotvednct01622205ablockrandomizedtrialwithsuperioritydesignofveryearlysupporteddischargeforpatientswithstroke
AT lundgrennilssonasa gothenburgveryearlysupporteddischargestudygotvednct01622205ablockrandomizedtrialwithsuperioritydesignofveryearlysupporteddischargeforpatientswithstroke
AT frojdkarin gothenburgveryearlysupporteddischargestudygotvednct01622205ablockrandomizedtrialwithsuperioritydesignofveryearlysupporteddischargeforpatientswithstroke