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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Detalles Bibliográficos
Autores principales: Mason, Alexina J., Grieve, Richard D., Richards-Belle, Alvin, Mouncey, Paul R., Harrison, David A., Carpenter, James R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Technical Advance
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7076973/
https://www.ncbi.nlm.nih.gov/pubmed/32183708
http://dx.doi.org/10.1186/s12874-020-00930-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7076973/
https://www.ncbi.nlm.nih.gov/pubmed/32183708
http://dx.doi.org/10.1186/s12874-020-00930-2

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