Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/26140
Full metadata record
DC FieldValueLanguage
dc.contributor.authorDaynes, E-
dc.contributor.authorBaldwin, M-
dc.contributor.authorGreening, NJ-
dc.contributor.authorYates, T-
dc.contributor.authorBishop, NC-
dc.contributor.authorMills, G-
dc.contributor.authorRoberts, M-
dc.contributor.authorHamrouni, M-
dc.contributor.authorPlekhanova, T-
dc.contributor.authorVogiatzis, I-
dc.contributor.authorEchevarria, C-
dc.contributor.authorNathu, R-
dc.contributor.authorMcAuley, HJC-
dc.contributor.authorLatimer, L-
dc.contributor.authorGlennie, J-
dc.contributor.authorChambers, F-
dc.contributor.authorPenfold, R-
dc.contributor.authorHume, E-
dc.contributor.authorMegaritis, D-
dc.contributor.authorAlexiou, C-
dc.contributor.authorPotthoff, S-
dc.contributor.authorHogg, MJ-
dc.contributor.authorHaighton, C-
dc.contributor.authorNichol, B-
dc.contributor.authorLeavy, OC-
dc.contributor.authorRichardson, M-
dc.contributor.authorElneima, O-
dc.contributor.authorSingapuri, A-
dc.contributor.authorSereno, M-
dc.contributor.authorSaunders, RM-
dc.contributor.authorHarris, VC-
dc.contributor.authorNolan, CM-
dc.contributor.authorBolton, C-
dc.contributor.authorHouchen-Wolloff, L-
dc.contributor.authorHarrison, EM-
dc.contributor.authorLone, N-
dc.contributor.authorQuint, J-
dc.contributor.authorChalmers, JD-
dc.contributor.authorHo, L-P-
dc.contributor.authorHorsley, A-
dc.contributor.authorMarks, M-
dc.contributor.authorPoinasamy, K-
dc.contributor.authorRamen, B-
dc.contributor.authorWain, LV-
dc.contributor.authorBrightling, C-
dc.contributor.authorMan, WD-C-
dc.contributor.authorEvans, R-
dc.contributor.authorSingh, SJ-
dc.date.accessioned2023-03-14T15:50:52Z-
dc.date.available2023-03-14T15:50:52Z-
dc.date.issued2023-01-26-
dc.identifier.citationDaynes, E., Baldwin, M., Greening, N.J. et al. (2023) 'The effect of COVID rehabilitation for ongoing symptoms Post HOSPitalisation with COVID-19 (PHOSP-R): protocol for a randomised parallel group controlled trial on behalf of the PHOSP consortium' in Trials., Vol. 24 (1)., pp.1-10. https://doi.org/10.1186/s13063-023-07093-7en_US
dc.identifier.urihttp://bura.brunel.ac.uk/handle/2438/26140-
dc.descriptionCorrection published: https://doi.org/10.1186/s13063-023-07132-3 | https://bura.brunel.ac.uk/handle/2438/26141-
dc.description.abstractIntroduction Many adults hospitalised with COVID-19 have persistent symptoms such as fatigue, breathlessness and brain fog that limit day-to-day activities. These symptoms can last over 2 years. Whilst there is limited controlled studies on interventions that can support those with ongoing symptoms, there has been some promise in rehabilitation interventions in improving function and symptoms either using face-to-face or digital methods, but evidence remains limited and these studies often lack a control group. Methods and analysis This is a nested single-blind, parallel group, randomised control trial with embedded qualitative evaluation comparing rehabilitation (face-to-face or digital) to usual care and conducted within the PHOSP-COVID study. The aim of this study is to determine the effectiveness of rehabilitation interventions on exercise capacity, quality of life and symptoms such as breathlessness and fatigue. The primary outcome is the Incremental Shuttle Walking Test following the eight week intervention phase. Secondary outcomes include measures of function, strength and subjective assessment of symptoms. Blood inflammatory markers and muscle biopsies are an exploratory outcome. The interventions last eight weeks and combine symptom-titrated exercise therapy, symptom management and education delivered either in a face-to-face setting or through a digital platform (www.yourcovidrecovery.nhs.uk). The proposed sample size is 159 participants, and data will be intention-to-treat analyses comparing rehabilitation (face-to-face or digital) to usual care. Ethics and dissemination Ethical approval was gained as part of the PHOSP-COVID study by Yorkshire and the Humber Leeds West Research NHS Ethics Committee, and the study was prospectively registered on the ISRCTN trial registry (ISRCTN13293865). Results will be disseminated to stakeholders, including patients and members of the public, and published in appropriate journals.en_US
dc.description.sponsorshipUK Research and Innovation and National Institute of Health Research (grant references: MR/V027859/1 and COV0319) and by core funding provided by NIHR Leicester Biomedical Research Centre—a partnership between the University Hospitals of Leicester NHS Trust, the University of Leicester and Loughborough University and by pump priming funding provided by Northumbria University Newcastle (MDRT IHSC and HLS Faculty).en_US
dc.languageen-
dc.publisherSpringer Science and Business Media LLCen_US
dc.rightsRights and permissions Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.-
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/-
dc.subjectCOVID-19en_US
dc.subjectRehabilitationen_US
dc.subjectDigitalen_US
dc.subjectRandomised controlled trialen_US
dc.titleThe effect of COVID rehabilitation for ongoing symptoms Post HOSPitalisation with COVID-19 (PHOSP-R): protocol for a randomised parallel group controlled trial on behalf of the PHOSP consortiumen_US
dc.typeArticleen_US
dc.identifier.doihttp://dx.doi.org/10.1186/s13063-023-07093-7-
dc.relation.isPartOfTrials-
pubs.issue1-
pubs.publication-statusPublished online-
pubs.volume24-
dc.identifier.eissn1745-6215-
Appears in Collections:Dept of Health Sciences Research Papers

Files in This Item:
File Description SizeFormat 
FullText.pdf© The Author(s) 2023. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativeco mmons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.1.14 MBAdobe PDFView/Open


This item is licensed under a Creative Commons License Creative Commons