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Variation in recruitment across sites in a consent-based clinical data registry: lessons from the Canadian Stroke Network

BACKGROUND: In earlier work, we found important selection biases when we tried to obtain consent for participation in a national stroke registry. Recognizing that not all registries will be exempt from requiring consent for participation, we examine here in greater depth the reasons for the poor acc...

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Detalles Bibliográficos
Autores principales: Willison, Donald J, Kapral, Moira K, Peladeau, Pierrot, Richards, Janice A, Fang, Jiming, Silver, Frank L
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1513239/
https://www.ncbi.nlm.nih.gov/pubmed/16716233
http://dx.doi.org/10.1186/1472-6939-7-6