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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Enregistré dans:
Détails bibliographiques
Publié dans:BMC Med Res Methodol
Auteurs principaux: Mason, Alexina J., Grieve, Richard D., Richards-Belle, Alvin, Mouncey, Paul R., Harrison, David A., Carpenter, James R.
Format: Artigo
Langue:Inglês
Publié: BioMed Central 2020
Sujets:
Technical Advance
Accès en ligne: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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