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dc.contributor.authorMarston, L
dc.contributor.authorLe Novere, M
dc.contributor.authorRicciardi, F
dc.contributor.authorNazareth, I
dc.contributor.authorCarson, A
dc.contributor.authorEdwards, M
dc.contributor.authorGoldstein, LH
dc.contributor.authorMarsden, Jonathan
dc.contributor.authorNoble, H
dc.contributor.authorReuber, M
dc.contributor.authorStone, J
dc.contributor.authorHunter, RM
dc.contributor.authorNielsen, G
dc.date.accessioned2023-04-28T14:07:14Z
dc.date.available2023-04-28T14:07:14Z
dc.date.issued2023-06
dc.identifier.issn2451-8654
dc.identifier.issn2451-8654
dc.identifier.other101124
dc.identifier.urihttps://pearl.plymouth.ac.uk/handle/10026.1/20769
dc.description.abstract

Introduction Functional motor disorder (FMD) is a common cause of disabling neurological symptoms such as weakness and tremor. Physio4FMD is a pragmatic, multicentre single blind randomised controlled trial to evaluate effectiveness and cost effectiveness of specialist physiotherapy for FMD. Like many other studies this trial was affected by the COVID-19 pandemic.

Methods The planned statistical and health economics analyses for this trial are described, as well as the sensitivity analyses designed to assess the disruption caused by COVID-19. The trial treatment of at least 89 participants (33%) was disrupted due to the pandemic. To account for this, we have extended the trial to increase the sample size. We have identified four groups based on how participants’ involvement in Physio4FMD was affected; A: 25 were unaffected; B: 134 received their trial treatment before the start of the COVID-19 pandemic and were followed up during the pandemic; C: 89 were recruited in early 2020 and had not received any randomised treatment before clinical services closed because of COVID-19; D: 88 participants were recruited after the trial was restarted in July 2021. The primary analysis will involve groups A, B and D. Regression analysis will be used to assess treatment effectiveness. We will conduct descriptive analyses for each of the groups identified and sensitivity regression analyses with participants from all groups, including group C, separately.

Discussion The COVID-19 mitigation strategy and analysis plans are designed to maintain the integrity of the trial while providing meaningful results.

dc.format.extent101124-101124
dc.format.mediumPrint-Electronic
dc.languageen
dc.publisherElsevier BV
dc.subjectCOVID-19
dc.subjectClinical trial
dc.subjectConversion disorder
dc.subjectFunctional neurological disorder
dc.subjectHealth economics
dc.subjectPhysiotherapy
dc.subjectRandomised controlled trial
dc.subjectStatistics
dc.titleCOVID-19 and the Physio4FMD trial: Impact, mitigating strategies and analysis plans
dc.typejournal-article
dc.typeJournal Article
plymouth.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/37008795
plymouth.volume33
plymouth.publication-statusPublished
plymouth.journalContemporary Clinical Trials Communications
dc.identifier.doi10.1016/j.conctc.2023.101124
plymouth.organisational-group|Plymouth
plymouth.organisational-group|Plymouth|Research Groups
plymouth.organisational-group|Plymouth|Faculty of Health
plymouth.organisational-group|Plymouth|Faculty of Health|School of Health Professions
plymouth.organisational-group|Plymouth|Research Groups|Institute of Health and Community
plymouth.organisational-group|Plymouth|REF 2021 Researchers by UoA
plymouth.organisational-group|Plymouth|Users by role
plymouth.organisational-group|Plymouth|Users by role|Academics
plymouth.organisational-group|Plymouth|REF 2021 Researchers by UoA|UoA03 Allied Health Professions, Dentistry, Nursing and Pharmacy
plymouth.organisational-group|Plymouth|Research Groups|FoH - Applied Parkinson's Research
dc.publisher.placeNetherlands
dcterms.dateAccepted2023-03-23
dc.date.updated2023-04-28T14:06:50Z
dc.rights.embargodate2023-4-29
dc.identifier.eissn2451-8654
dc.rights.embargoperiodforever
rioxxterms.versionofrecord10.1016/j.conctc.2023.101124


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