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dc.contributor.authorBhattacharya, IS
dc.contributor.authorHaviland, JS
dc.contributor.authorTurner, L
dc.contributor.authorStobart, H
dc.contributor.authorBalasopoulou, A
dc.contributor.authorStones, L
dc.contributor.authorKirby, AM
dc.contributor.authorKirwan, CC
dc.contributor.authorColes, CE
dc.contributor.authorBliss, JM
dc.contributor.authorPRIMETIME Trialists,
dc.date.accessioned2021-08-10T14:18:46Z
dc.date.available2021-08-10T14:18:46Z
dc.date.issued2021-06-14
dc.identifier.citationTrials, 2021, 22 pp. 397 - 397
dc.identifier.issn1745-6215
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/4731
dc.identifier.doi10.1186/s13063-021-05345-y
dc.description.abstractBACKGROUND: For patients with early breast cancer considered at very-low risk of local relapse, risks of radiotherapy may outweigh the benefits. Decisions regarding treatment omission can lead to patient uncertainty (decisional conflict), which may be lessened with patient decision aids (PDA). PRIMETIME (ISRCTN 41579286) is a UK-led biomarker-directed study evaluating omission of adjuvant radiotherapy in breast cancer; an embedded Study Within A Trial (SWAT) investigated whether PDA reduces decisional conflict using a cluster stepped-wedge trial design. METHODS: PDA diagrams and a video explaining risks and benefits of radiotherapy were developed in close collaboration between patient advocates and PRIMETIME trialists. The SWAT used a cluster stepped-wedge trial design, where each cluster represented the radiotherapy centre and referring peripheral centres. All clusters began in the standard information group (patient information and diagrams) and were randomised to cross-over to the enhanced information group (standard information plus video) at 2, 4 or 6 months. Primary endpoint was the decisional conflict scale (0-100, higher scores indicating greater conflict) which was assessed on an individual participant level. Multilevel mixed effects models used a random effect for cluster and a fixed effect for each step to adjust for calendar time and clustering. Robust standard errors were also adjusted for the clustering effect. RESULTS: Five hundred twenty-one evaluable questionnaires were returned from 809 eligible patients (64%) in 24 clusters between April 2018 and October 2019. Mean decisional conflict scores in the standard group (N = 184) were 10.88 (SD 11.82) and 8.99 (SD 11.82) in the enhanced group (N = 337), with no statistically significant difference [mean difference - 1.78, 95%CI - 3.82-0.25, p = 0.09]. Compliance with patient information and diagrams was high in both groups although in the enhanced group only 121/337 (36%) reported watching the video. CONCLUSION: The low levels of decisional conflict in PRIMETIME are reassuring and may reflect the high-quality information provision, such that not everyone required the video. This reinforces the importance of working with patients as partners in clinical trials especially in the development of patient-centred information and decision aids.
dc.format.extent397 - 397
dc.languageeng
dc.language.isoeng
dc.publisherBMC
dc.relation.isreplacedbyinternal/5048
dc.relation.isreplacedbyhttps://repository.icr.ac.uk/handle/internal/5048
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.titleCan patient decision aids reduce decisional conflict in a de-escalation of breast radiotherapy clinical trial? The PRIMETIME Study Within a Trial implemented using a cluster stepped-wedge trial design.
dc.typeJournal Article
dcterms.dateAccepted2021-05-29
rioxxterms.versionVoR
rioxxterms.versionofrecord10.1186/s13063-021-05345-y
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2021-06-16
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfTrials
pubs.notesNo embargo
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Clinical Trials & Statistics Unit
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Clinical Trials & Statistics Unit
pubs.publication-statusPublished
pubs.volume22
pubs.embargo.termsNo embargo
icr.researchteamClinical Trials & Statistics Unit
icr.researchteamClinical Trials & Statistics Unit
dc.contributor.icrauthorHaviland, Joanne
dc.contributor.icrauthorBliss, Judith


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