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Using Trial Sequential Analysis for estimating the sample sizes of further trials: example using smoking cessation intervention
BACKGROUND: Assessing benefits and harms of health interventions is resource-intensive and often requires feasibility and pilot trials followed by adequately powered randomised clinical trials. Data from feasibility and pilot trials are used to inform the design and sample size of the adequately pow...
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| Publicado en: | BMC Med Res Methodol |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
BioMed Central
2020
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7702700/ https://ncbi.nlm.nih.gov/pubmed/33256626 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12874-020-01169-7 |
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