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dc.contributor.authorJull, Janet
dc.contributor.authorYoganathan, Manosila
dc.contributor.authorDewidar, Omar
dc.contributor.authorBaird, Sarah
dc.contributor.authorGrimshaw, Jeremy M.
dc.contributor.authorJohansson, Kjell Arne
dc.contributor.authorKristjansson, Elizabeth
dc.contributor.authorMcGowan, Jesse
dc.contributor.authorMoher, David
dc.contributor.authorPetticrew, Mark
dc.contributor.authorRobberstad, Bjarne
dc.contributor.authorShea, Beverly
dc.contributor.authorTugwell, Peter
dc.contributor.authorVolmink, Jimmy
dc.contributor.authorWells, George A.
dc.contributor.authorWhitehead, Margaret
dc.contributor.authorCuervo, Luis Gabriel
dc.contributor.authorWhite, Howard
dc.contributor.authorTaljaard, Monica
dc.contributor.authorWelch, Vivian
dc.contributor.authorPetkovic, Jennifer
dc.date.accessioned2021-08-17T08:34:35Z
dc.date.available2021-08-17T08:34:35Z
dc.date.created2021-02-05T11:06:34Z
dc.date.issued2020
dc.identifier.issn1745-6215
dc.identifier.urihttps://hdl.handle.net/11250/2768693
dc.description.abstractBackground The randomized controlled trial (RCT) is considered the gold standard study design to inform decisions about the effectiveness of interventions. However, a common limitation is inadequate reporting of the applicability of the intervention and trial results for people who are “socially disadvantaged” and this can affect policy-makers’ decisions. We previously developed a framework for identifying health-equity-relevant trials, along with a reporting guideline for transparent reporting. In this study, we provide a descriptive assessment of health-equity considerations in 200 randomly sampled equity-relevant trials. Methods We developed a search strategy to identify health-equity-relevant trials published between 2013 and 2015. We randomly sorted the 4316 records identified by the search and screened studies until 100 individually randomized (RCTs) and 100 cluster randomized controlled trials (CRTs) were identified. We developed and pilot-tested a data extraction form based on our initial work, to inform the development of our reporting guideline for equity-relevant randomized trials. Results In total, 39 trials (20%) were conducted in a low- and middle-income country and 157 trials (79%) in a high-income country focused on socially disadvantaged populations (78% CRTs, 79% RCTs). Seventy-four trials (37%) reported a subgroup analysis across a population characteristic associated with disadvantage (25% CRT, 49% RCTs), with 19% of included studies reporting subgroup analyses across sex, 9% across race/ethnicity/culture, and 4% across socioeconomic status. No subgroup analyses were reported for place of residence, occupation, religion, education, or social capital. One hundred and forty-one trials (71%) discussed the applicability of their results to one or more socially disadvantaged populations (68% of CRT, 73% of RCT). Discussion In this set of trials, selected for their relevance to health equity, data that were disaggregated for socially disadvantaged populations were rarely reported. We found that even when the data are available, opportunities to analyze health-equity considerations are frequently missed. The recently published equity extension of the Consolidated Reporting Standards for Randomized Trials (CONSORT-Equity) may help improve delineation of hypotheses related to socially disadvantaged populations, and transparency and completeness of reporting of health-equity considerations in RCTs. This study can serve as a baseline assessment of the reporting of equity considerations.en_US
dc.language.isoengen_US
dc.publisherBMCen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleReporting of health equity considerations in cluster and individually randomized trialsen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright The Author(s). 2020en_US
dc.source.articlenumber308en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doi10.1186/s13063-020-4223-5
dc.identifier.cristin1887053
dc.source.journalTrialsen_US
dc.identifier.citationTrials. 2020, 21, 308.en_US
dc.source.volume21en_US


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