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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Vydáno v:BMC Med Res Methodol
Hlavní autoři: Mason, Alexina J., Grieve, Richard D., Richards-Belle, Alvin, Mouncey, Paul R., Harrison, David A., Carpenter, James R.
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2020
Témata:
Technical Advance
On-line přístup: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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