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Cognitive rehabilitation in post-COVID-19 condition: A study protocol for a randomized controlled trial
BACKGROUND: Post-COVID-19 condition is frequently comprised of persistent cognitive sequela, including deficits in attention and executive functions (EFs), which can act as a barrier for regaining pre-illness functional levels. Goal Management Training (GMT) is a cognitive rehabilitation (CR) interv...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Authors. Published by Elsevier Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9533592/ https://www.ncbi.nlm.nih.gov/pubmed/36208718 http://dx.doi.org/10.1016/j.cct.2022.106955 |
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author | Hagen, Bjørn Ingulfsvann Lerdal, Anners Søraas, Arne Landrø, Nils Inge Bø, Ragnhild Småstuen, Milada Cvancarova Becker, Jacqueline Stubberud, Jan |
author_facet | Hagen, Bjørn Ingulfsvann Lerdal, Anners Søraas, Arne Landrø, Nils Inge Bø, Ragnhild Småstuen, Milada Cvancarova Becker, Jacqueline Stubberud, Jan |
author_sort | Hagen, Bjørn Ingulfsvann |
collection | PubMed |
description | BACKGROUND: Post-COVID-19 condition is frequently comprised of persistent cognitive sequela, including deficits in attention and executive functions (EFs), which can act as a barrier for regaining pre-illness functional levels. Goal Management Training (GMT) is a cognitive rehabilitation (CR) intervention for improving attention and EFs that has received empirical support in studies of other patient groups. The present study aims to determine the efficacy of GMT for improving everyday attention and EFs in adults who experience persistent cognitive deficits after COVID-19. METHODS: This study protocol describes an open-label randomized controlled trial comparing the efficacy of GMT to a wait list control condition (WL), for improving persistent (> 2 months) cognitive sequela in post-COVID-19 condition. The study aims to recruit 240 participants aged 18 to 65 years with a history of SARS-CoV-2 infection and perceived attentional and EF difficulties in daily life. Participants will be block randomized (computer-algorithm) to either group-based GMT (n = 120) or WL (n = 120). GMT will be internet-delivered to groups of six participants in six two-hour sessions delivered once a week. The primary outcome will be the Metacognition Index of the Behavior Rating Inventory of Executive Function – Adult Version, a self-report measure assessing everyday EF difficulties, specifically metacognition, at six months post-treatment. Secondary outcomes include performance-based neurocognitive measures, and tertiary outcomes include rating scales of cognition, emotional health, quality of life, and fatigue. CONCLUSION: Study findings could contribute to providing an evidence-based treatment option for symptoms that are frequent and debilitating following a prevalent condition. TRIAL REGISTRATION NUMBER: NCT05494424 |
format | Online Article Text |
id | pubmed-9533592 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Authors. Published by Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95335922022-10-05 Cognitive rehabilitation in post-COVID-19 condition: A study protocol for a randomized controlled trial Hagen, Bjørn Ingulfsvann Lerdal, Anners Søraas, Arne Landrø, Nils Inge Bø, Ragnhild Småstuen, Milada Cvancarova Becker, Jacqueline Stubberud, Jan Contemp Clin Trials Article BACKGROUND: Post-COVID-19 condition is frequently comprised of persistent cognitive sequela, including deficits in attention and executive functions (EFs), which can act as a barrier for regaining pre-illness functional levels. Goal Management Training (GMT) is a cognitive rehabilitation (CR) intervention for improving attention and EFs that has received empirical support in studies of other patient groups. The present study aims to determine the efficacy of GMT for improving everyday attention and EFs in adults who experience persistent cognitive deficits after COVID-19. METHODS: This study protocol describes an open-label randomized controlled trial comparing the efficacy of GMT to a wait list control condition (WL), for improving persistent (> 2 months) cognitive sequela in post-COVID-19 condition. The study aims to recruit 240 participants aged 18 to 65 years with a history of SARS-CoV-2 infection and perceived attentional and EF difficulties in daily life. Participants will be block randomized (computer-algorithm) to either group-based GMT (n = 120) or WL (n = 120). GMT will be internet-delivered to groups of six participants in six two-hour sessions delivered once a week. The primary outcome will be the Metacognition Index of the Behavior Rating Inventory of Executive Function – Adult Version, a self-report measure assessing everyday EF difficulties, specifically metacognition, at six months post-treatment. Secondary outcomes include performance-based neurocognitive measures, and tertiary outcomes include rating scales of cognition, emotional health, quality of life, and fatigue. CONCLUSION: Study findings could contribute to providing an evidence-based treatment option for symptoms that are frequent and debilitating following a prevalent condition. TRIAL REGISTRATION NUMBER: NCT05494424 The Authors. Published by Elsevier Inc. 2022-11 2022-10-05 /pmc/articles/PMC9533592/ /pubmed/36208718 http://dx.doi.org/10.1016/j.cct.2022.106955 Text en © 2022 The Authors Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Hagen, Bjørn Ingulfsvann Lerdal, Anners Søraas, Arne Landrø, Nils Inge Bø, Ragnhild Småstuen, Milada Cvancarova Becker, Jacqueline Stubberud, Jan Cognitive rehabilitation in post-COVID-19 condition: A study protocol for a randomized controlled trial |
title | Cognitive rehabilitation in post-COVID-19 condition: A study protocol for a randomized controlled trial |
title_full | Cognitive rehabilitation in post-COVID-19 condition: A study protocol for a randomized controlled trial |
title_fullStr | Cognitive rehabilitation in post-COVID-19 condition: A study protocol for a randomized controlled trial |
title_full_unstemmed | Cognitive rehabilitation in post-COVID-19 condition: A study protocol for a randomized controlled trial |
title_short | Cognitive rehabilitation in post-COVID-19 condition: A study protocol for a randomized controlled trial |
title_sort | cognitive rehabilitation in post-covid-19 condition: a study protocol for a randomized controlled trial |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9533592/ https://www.ncbi.nlm.nih.gov/pubmed/36208718 http://dx.doi.org/10.1016/j.cct.2022.106955 |
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