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dc.contributor.authorZhu, Lin
dc.contributor.authorBell, Katy J.L.
dc.contributor.authorHayen, Andrew
dc.date.accessioned2021-04-14T06:53:11Z
dc.date.available2021-04-14T06:53:11Z
dc.date.issued2019en
dc.identifier.urihttps://hdl.handle.net/2123/24923
dc.description.abstract“Legacy effects” describe the phenomena where treatment effects are apparent during the post-trial period that are not attributable to the direct effects observed within the trial. We investigate different approaches to analysis of trial and extended follow-up data for the evaluation of legacy effects. We conducted a simulation to compare three approaches, which differed in terms of the time period and selection of trial participants included in the analysis.en
dc.language.isoenen
dc.publisherElsevieren
dc.relation.ispartofJournal of Clinical Epidemiologyen
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivatives 4.0en
dc.subjectLegacy effectsen
dc.subjectrandomised control trialen
dc.subjectPost-trial follow-upen
dc.subjectcardiovascular diseaseen
dc.titleEstimated legacy effects from simulated post-trial data were less biased than from combined trial/post-trial data.en
dc.typeArticleen
dc.subject.asrc1102 Cardiorespiratory Medicine and Haematologyen
dc.subject.asrc1117 Public Health and Health Servicesen
dc.identifier.doi10.1016/j.jclinepi.2019.05.010
dc.relation.nhmrc1104136
usyd.facultySeS faculties schools::Faculty of Medicine and Health::Sydney School of Public Healthen
usyd.citation.volume114en
usyd.citation.spage30en
usyd.citation.epage37en
workflow.metadata.onlyNoen


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