Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/117784
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dc.contributorDepartment of Applied Mathematics-
dc.creatorYan, J-
dc.creatorHumphries, B-
dc.creatorXie, R-
dc.creatorYin, Z-
dc.creatorBo, Z-
dc.creatorDiao, S-
dc.creatorCai, J-
dc.creatorTse, P-
dc.creatorLi, M-
dc.creatorPullenayegum, E-
dc.creatorLee, SF-
dc.creatorXie, F-
dc.date.accessioned2026-03-05T07:56:25Z-
dc.date.available2026-03-05T07:56:25Z-
dc.identifier.issn1098-3015-
dc.identifier.urihttp://hdl.handle.net/10397/117784-
dc.language.isoenen_US
dc.publisherElsevier BVen_US
dc.rights© 2025, International Society for Pharmacoeconomics and Outcomes Research, Inc. Published by Elsevier Inc. This is an open access article under theCC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).en_US
dc.rightsThe following publication Yan, J., Humphries, B., Xie, R., Yin, Z., Bo, Z., Diao, S., Cai, J., Tse, P., Li, M., Pullenayegum, E., Lee, S. F., & Xie, F. (2025). Statistical Methods for Analyzing EQ-5D in Randomized Clinical Trials: A Systematic Literature Review. Value in Health, 28(7), 1126–1135 is available at https://doi.org/10.1016/j.jval.2025.02.001.en_US
dc.subjectEQ-5Den_US
dc.subjectPatient-reported outcomeen_US
dc.subjectRandomized clinical trialen_US
dc.subjectStatistical analysisen_US
dc.titleStatistical methods for analyzing EQ-5D in randomized clinical trials : a systematic literature reviewen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage1126-
dc.identifier.epage1135-
dc.identifier.volume28-
dc.identifier.issue7-
dc.identifier.doi10.1016/j.jval.2025.02.001-
dcterms.abstractObjectives: We conducted a systematic literature review to summarize the application of statistical methods for analyzing treatment effect on EQ-5D in randomized clinical trials (RCTs).-
dcterms.abstractMethod: We searched 2 electronic databases (MEDLINE and EMBASE, from inception through 2021) and www.clinicaltrial.gov. Eligible studies were RCTs that analyzed postbaseline EQ-5D data by treatment group. Information on trial characteristics, EQ-5D data characteristics, and statistical methods were extracted. Descriptive statistics were used to summarize results by dimension response, EQ visual analog scale (EQ VAS), and EQ-5D utility.-
dcterms.abstractResults: A total of 2125 trials met the eligibility criteria. EQ-5D was commonly considered a secondary (n = 1219, 57.4%) or exploratory (n = 775, 36.5%) endpoint in RCTs. EQ-5D utilities were the most analyzed. Both utilities and EQ VAS were primarily analyzed in numerical format. The most common statistical models for analyzing utilities were the linear fixed-effect model for single postbaseline (192/589, 32.6%) and the linear mixed-effect model for multiple post-baselines (338/984, 34.3%). Of the 2054 studies that analyzed numerical EQ-5D, 221 (10.8%) examined model assumptions and 438 (21.3%) adjusted for the baseline score. Missing data were explicitly assessed in 661 trials, among which 347 (52.5% of 661) applied imputations, with the 2 most used imputation methods being multiple imputations (n = 200, 57.6% of 347) and last observation carried forward (n = 106, 30.5% of 347).-
dcterms.abstractConclusions: This review found that health utilities are the most frequently analyzed EQ-5D data collected in clinical trials, followed by EQ VAS. Significant variation was observed in the selection of models, with most trials lacking adjustments for baseline data and appropriate methods for handling missing data.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationValue in health, July 2025, v. 28, no. 7, p. 1126-1135-
dcterms.isPartOfValue in health-
dcterms.issued2025-07-
dc.identifier.scopus2-s2.0-105000350017-
dc.identifier.pmid39954858-
dc.identifier.eissn1524-4733-
dc.description.validate202603 bcch-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOSen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextThis study was funded by a PhD grant from the EuroQol Research Foundation (# 345-PHD).en_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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