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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:BMC Med Res Methodol
Egile Nagusiak: Mason, Alexina J., Grieve, Richard D., Richards-Belle, Alvin, Mouncey, Paul R., Harrison, David A., Carpenter, James R.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BioMed Central 2020
Gaiak:
Technical Advance
Sarrera elektronikoa: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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