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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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| Publicado no: | BMC Med Res Methodol |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2020
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| Assuntos: | |
| Acesso em linha: | 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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