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  2. Consolidated Standards of Reporting Trials - Wikipedia

    en.wikipedia.org/wiki/Consolidated_Standards_of...

    The main product of the CONSORT Group is the CONSORT Statement, [1] which is an evidence-based, minimum set of recommendations for reporting randomized trials.It offers a standard way for authors to prepare reports of trial findings, facilitating their complete and transparent reporting, reducing the influence of bias on their results, and aiding their critical appraisal and interpretation.

  3. Strengthening the reporting of observational studies in ...

    en.wikipedia.org/wiki/Strengthening_the...

    In 2010, three years after STROBE's publication, the original creators reconvened and deemed an update unnecessary at the time. [21] However, since, calls have supported for the reporting guideline to be updated, similarly to other reporting guidelines (like CONSORT and PRISMA ) which have been updated as needed.

  4. Virginia Barbour - Wikipedia

    en.wikipedia.org/wiki/Virginia_Barbour

    CONSORT 2010 statement: updated guidelines for reporting parallel group randomised trials [12] CONSORT 2010 explanation and elaboration: updated guidelines for reporting parallel group randomised trials. 2012. International Journal of Surgery. [citation needed]

  5. Randomized controlled trial - Wikipedia

    en.wikipedia.org/wiki/Randomized_controlled_trial

    Consort 2010 Statement: Extension to Cluster Randomised Trials [74] Consort 2010 Statement: Non-Pharmacologic Treatment Interventions [ 75 ] [ 76 ] "Reporting of surrogate endpoints in randomised controlled trial reports (CONSORT-Surrogate): extension checklist with explanation and elaboration" [ 77 ]

  6. Preferred Reporting Items for Systematic Reviews and Meta ...

    en.wikipedia.org/wiki/Preferred_reporting_items...

    The PRISMA flow diagram, depicting the flow of information through the different phases of a systematic review. PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) is an evidence-based minimum set of items aimed at helping scientific authors to report a wide array of systematic reviews and meta-analyses, primarily used to assess the benefits and harms of a health care ...

  7. Isabelle Boutron - Wikipedia

    en.wikipedia.org/wiki/Isabelle_Boutron

    She has worked on the internal and external validity of non-pharmacological trials, and co-led the extension of the CONSORT statement on reporting treatment trials for nonpharmacologic treatments. [ 2 ] [ 3 ] Along with her colleagues she edited a book entitled “Randomized Clinical Trials of Nonpharmacological Treatments.”

  8. What is a royal consort? - AOL

    www.aol.com/royal-consort-184208580.html

    A royal consort is the spouse of a serving monarch, whose main duty is to provide support and companionship during their reign. Unlike the king or queen, they do not have a formal position or set ...

  9. Risk difference - Wikipedia

    en.wikipedia.org/wiki/Risk_difference

    The adverse outcome (black) risk difference between the group exposed to the treatment (left) and the group unexposed to the treatment (right) is −0.25 (RD = −0.25, ARR = 0.25).