Comparar métodos
Examine os métodos selecionados lado a lado; as linhas que diferem ficam destacadas.
| Ensaio Clínico Randomizado Simplesmente Cegado× | Ensaio Clínico Randomizado Pragmático× | |
|---|---|---|
| Área | Delineamento experimental | Delineamento experimental |
| Família | Process / pipeline | Process / pipeline |
| Ano de origem≠ | 1948 (formalized); single-blind variant established in mid-20th century clinical trial methodology | 1967 |
| Autor original≠ | Bradford Hill and colleagues (MRC streptomycin trial, 1948); blinding conventions codified in CONSORT guidelines | Daniel Schwartz and Joseph Lellouch |
| Tipo≠ | Experimental design — blinded randomized trial | Experimental design — pragmatic trial |
| Fonte seminal≠ | Schulz, K. F., Altman, D. G., Moher, D., & CONSORT Group. (2010). CONSORT 2010 statement: Updated guidelines for reporting parallel group randomised trials. BMJ, 340, c332. DOI ↗ | Schwartz, D., & Lellouch, J. (1967). Explanatory and pragmatic attitudes in therapeutical trials. Journal of Chronic Diseases, 20(8), 637–648. DOI ↗ |
| Outros nomes | single-masked RCT, single-blind RCT, single-blind trial, SB-RCT | pRCT, pragmatic trial, practical clinical trial, real-world RCT |
| Relacionados≠ | 5 | 4 |
| Resumo≠ | A single-blind randomized controlled trial (SB-RCT) is a rigorous experimental design in which participants are randomly assigned to treatment or control conditions while remaining unaware of which condition they have received. Investigators, outcome assessors, and data analysts are not blinded. By masking participants, the design eliminates placebo and nocebo response biases on the participant side, while preserving investigator flexibility to administer and monitor the intervention. | A pragmatic randomized controlled trial (pRCT) tests whether an intervention works under ordinary, real-world conditions — broad eligibility, flexible delivery, and routine care settings. Participants are still randomly assigned to treatment or control, preserving causal inference, but the study is designed to reflect the diversity and variability of actual practice rather than the ideal conditions of an explanatory trial. The defining framework is the PRECIS-2 tool, which maps any RCT along nine pragmatic-to-explanatory dimensions. |
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