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Telehealth-delivered cognitive rehabilitation for people with cognitive impairment as part of the post-COVID syndrome: protocol for a randomised controlled trial as part of the CICERO (Cognitive Impairment in Long COVID: Phenotyping and Rehabilitation) study

Crossref DOI link: https://doi.org/10.1186/s13063-024-08554-3

Published Online: 2024-10-22

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Vanova, Martina https://orcid.org/0000-0002-1329-7566
Patel, Aysha Mohamed Rafik https://orcid.org/0009-0004-4987-8217
Scott, Iona

Gilpin, Gina https://orcid.org/0000-0002-9441-7979
Manning, Emily N. https://orcid.org/0000-0002-4505-3611
Ash, Charlotte https://orcid.org/0009-0007-2591-9637
Wittenberg, Philippa https://orcid.org/0009-0003-8583-7896
Lim, Jason https://orcid.org/0000-0001-6397-3131
Hoare, Zoe https://orcid.org/0000-0003-1803-5482
Evans, Rachel https://orcid.org/0000-0003-0960-9843
Bray, Nathan https://orcid.org/0000-0001-7646-5435
Kipps, Christopher M. https://orcid.org/0000-0002-5205-9712
Devine, Ciara https://orcid.org/0009-0008-9107-1045
Ahmed, Saliha

Dunne, Ross

Koniotes, Anna https://orcid.org/0009-0000-7009-6456
Warren, Catherine https://orcid.org/0009-0002-0119-820X
Chan, Dennis https://orcid.org/0000-0002-4265-3718
Suarez-Gonzalez, Aida https://orcid.org/0000-0002-0904-1031
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Text and Data Mining valid from 2024-10-22

Version of Record valid from 2024-10-22
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Article History

Received: 27 June 2024

Accepted: 14 October 2024

First Online: 22 October 2024

Declarations

:

: The study has received ethics approval from the East England – Essex Research Ethics Committee (reference: 22/EE/0074; IRAS Project ID: 302920). NHS Management Approval has also been given. The study will be conducted in accordance with the Declaration of Helsinki and has been presented to the East of England - Essex Research Ethics Committee (registration number 22/EE/0074). Signed written informed consent will be provided by all participants, gathered online before the commencement of the baseline assessment. Authors MV, AMRP, IS, and GG will inform participants about the study and request consent.

: Model consent forms for all participants tested within the trial on cognitive measures (Informed Consent Form - ICF Workstream 1), participants eligible for RCT (ICF Workstream 2), and control participants to be included in the workshops (ICF Workshop for controls) are included in the Appendix.

: The authors declare no competing interests.

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