dc.contributor.author | Ingulfsvann Hagen, Bjørn | |
dc.contributor.author | Lerdal, Anners | |
dc.contributor.author | Søraas, Arne Vasli | |
dc.contributor.author | Landrø, Nils Inge | |
dc.contributor.author | Bø, Ragnhild | |
dc.contributor.author | Småstuen, Milada Cvancarova | |
dc.contributor.author | Becker, Jaqueline | |
dc.contributor.author | Stubberud, Jan Egil | |
dc.date.accessioned | 2022-12-09T11:41:50Z | |
dc.date.available | 2022-12-09T11:41:50Z | |
dc.date.issued | 2022-10-05 | |
dc.description.abstract | 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.<p>
<p>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.
<p>Conclusion: Study findings could contribute to providing an evidence-based treatment option for symptoms that
are frequent and debilitating following a prevalent condition. | en_US |
dc.identifier.citation | Ingulfsvann Hagen BOI, Lerdal AL, Søraas AVL, Landrø NI, Bø R, Småstuen MC, Becker J, Stubberud J. Cognitive rehabilitation in post-COVID-19 condition: A study protocol for a randomized controlled trial. Contemporary Clinical Trials. 2022;122 | en_US |
dc.identifier.cristinID | FRIDAID 2061109 | |
dc.identifier.doi | 10.1016/j.cct.2022.106955 | |
dc.identifier.issn | 1551-7144 | |
dc.identifier.issn | 1559-2030 | |
dc.identifier.uri | https://hdl.handle.net/10037/27758 | |
dc.language.iso | eng | en_US |
dc.publisher | Elsevier | en_US |
dc.relation.journal | Contemporary Clinical Trials | |
dc.rights.accessRights | openAccess | en_US |
dc.rights.holder | Copyright 2022 The Author(s) | en_US |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0 | en_US |
dc.rights | Attribution 4.0 International (CC BY 4.0) | en_US |
dc.title | Cognitive rehabilitation in post-COVID-19 condition: A study protocol for a randomized controlled trial | en_US |
dc.type.version | publishedVersion | en_US |
dc.type | Journal article | en_US |
dc.type | Tidsskriftartikkel | en_US |
dc.type | Peer reviewed | en_US |