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dc.contributor.authorBoutron, Ien_US
dc.contributor.authorAltman, DGen_US
dc.contributor.authorMoher, Den_US
dc.contributor.authorSchulz, KFen_US
dc.contributor.authorRavaud, Pen_US
dc.contributor.authorCONSORT NPT Groupen_US
dc.date.accessioned2017-06-27T14:13:44Z
dc.date.available2017-01-06en_US
dc.date.issued2017-07-04en_US
dc.date.submitted2017-06-19T14:48:00.888Z
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/24601
dc.descriptionKam Bhui is part of the Consort group
dc.descriptionKam Bhui is part of the Consort group
dc.descriptionKam Bhui is part of the Consort groupen_US
dc.descriptionKam Bhui is part of the Consort groupen_US
dc.description.abstractIncomplete and inadequate reporting is an avoidable waste that reduces the usefulness of research. The CONSORT (Consolidated Standards of Reporting Trials) Statement is an evidence-based reporting guideline that aims to improve research transparency and reduce waste. In 2008, the CONSORT Group developed an extension to the original statement that addressed methodological issues specific to trials of nonpharmacologic treatments (NPTs), such as surgery, rehabilitation, or psychotherapy. This article describes an update of that extension and presents an extension for reporting abstracts of NPT trials. To develop these materials, the authors reviewed pertinent literature published up to July 2016; surveyed authors of NPT trials; and conducted a consensus meeting with editors, trialists, and methodologists. Changes to the CONSORT Statement extension for NPT trials include wording modifications to improve readers' understanding and the addition of 3 new items. These items address whether and how adherence of participants to interventions is assessed or enhanced, description of attempts to limit bias if blinding is not possible, and specification of the delay between randomization and initiation of the intervention. The CONSORT extension for abstracts of NPT trials includes 2 new items that were not specified in the original CONSORT Statement for abstracts. The first addresses reporting of eligibility criteria for centers where the intervention is performed and for care providers. The second addresses reporting of important changes to the intervention versus what was planned. Both the updated CONSORT extension for NPT trials and the CONSORT extension for NPT trial abstracts should help authors, editors, and peer reviewers improve the transparency of NPT trial reports.en_US
dc.format.extent40 - 47en_US
dc.languageengen_US
dc.language.isoenen_US
dc.relation.ispartofAnn Intern Meden_US
dc.subjectPublishingen_US
dc.subjectQuality Controlen_US
dc.subjectRandomized Controlled Trials as Topicen_US
dc.subjectResearch Designen_US
dc.subjectTherapeuticsen_US
dc.titleCONSORT Statement for Randomized Trials of Nonpharmacologic Treatments: A 2017 Update and a CONSORT Extension for Nonpharmacologic Trial Abstracts.en_US
dc.typeArticle
dc.rights.holder(c)
dc.identifier.doi10.7326/M17-0046en_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/28630973en_US
pubs.issue1en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume167en_US


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