A framework for extending trial design to facilitate missing data sensitivity analyses

BACKGROUND: Missing data are an inevitable challenge in Randomised Controlled Trials (RCTs), particularly those with Patient Reported Outcome Measures. Methodological guidance suggests that to avoid incorrect conclusions, studies should undertake sensitivity analyses which recognise that data may be...

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Bibliografiset tiedot
Julkaisussa:BMC Med Res Methodol
Päätekijät: Mason, Alexina J., Grieve, Richard D., Richards-Belle, Alvin, Mouncey, Paul R., Harrison, David A., Carpenter, James R.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioMed Central 2020
Aiheet:
Technical Advance
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC7076973/
https://ncbi.nlm.nih.gov/pubmed/32183708
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12874-020-00930-2
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