A novel application of the Intent to Attend assessment to reduce bias due to missing data in a randomized controlled clinical trial

BACKGROUND: Missing data are unavoidable in most randomized controlled clinical trials, especially when measurements are taken repeatedly. If strong assumptions about the missing data are not accurate, crude statistical analyses are biased and can lead to false inferences. Furthermore, if we fail to...

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Pubblicato in:Clin Trials
Autori principali: Rabideau, Dustin J, Nierenberg, Andrew A, Sylvia, Louisa G, Friedman, Edward S., Bowden, Charles L., Thase, Michael E., Ketter, Terence, Ostacher, Michael J., Reilly-Harrington, Noreen, Iosifescu, Dan V., Calabrese, Joseph R., Leon, Andrew C., Schoenfeld, David A
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2014
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Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4247354/
https://ncbi.nlm.nih.gov/pubmed/24872362
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1740774514531096
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