Σύγκριση μεθόδων
Εξετάστε τις επιλεγμένες μεθόδους δίπλα-δίπλα· οι γραμμές που διαφέρουν επισημαίνονται.
| Πραγματιστική Κλινική Δοκιμή× | Τυχαιοποιημένη Ελεγχόμενη Δοκιμή (ΤΕΔ)× | |
|---|---|---|
| Πεδίο≠ | Κλινική Έρευνα | Πειραματικός Σχεδιασμός |
| Οικογένεια≠ | Process / pipeline | Hypothesis test |
| Έτος προέλευσης≠ | 2009-2015 | 1948 |
| Δημιουργός≠ | Thorpe et al. (2009); PRECIS framework developed by international consortia | James Lind (early precursor, 1747); modern formulation: Austin Bradford Hill & Medical Research Council (1948) |
| Τύπος≠ | Research Design | Interventional comparative study |
| Θεμελιώδης πηγή≠ | Thorpe, K. E., Zwarenstein, M., Oxman, A. D., Treweek, S., Furberg, C. D., Altman, D. G., ... & Tugwell, P. (2009). A pragmatic-explanatory continuum indicator summary (PRECIS): a tool to help trial designers. CMAJ, 180(10), E47–E57. DOI ↗ | Schulz, K.F., Altman, D.G., Moher, D., for the CONSORT Group (2010). CONSORT 2010 Statement: Updated Guidelines for Reporting Parallel Group Randomised Trials. BMJ, 340, c332. DOI ↗ |
| Εναλλακτικές ονομασίες | pragmatic trial, real-world trial, effectiveness trial, PRECIS-2 | RCT, randomised controlled trial, clinical trial, Randomize Kontrollü Çalışma (RCT) Tasarımı |
| Συναφείς≠ | 4 | 7 |
| Σύνοψη≠ | A pragmatic trial is designed to evaluate the real-world effectiveness of an intervention in typical clinical settings with diverse, representative patients, minimal exclusion criteria, and clinically relevant outcomes. Developed by Thorpe and colleagues (2009) and formalized via the PRECIS-2 framework (2015), pragmatic trials bridge the gap between explanatory efficacy trials (conducted in controlled research settings) and implementation science, answering the question 'Does this work in actual clinical practice?' rather than 'Can this work under ideal conditions?' | A randomized controlled trial (RCT) is the gold standard experimental design in clinical and health research, in which participants are randomly allocated to a treatment group or a control group so that the effect of an intervention can be measured with the highest possible degree of internal validity. The modern parallel-group RCT was formalized by Austin Bradford Hill and the Medical Research Council in their landmark streptomycin trial of 1948, and its reporting is governed today by the CONSORT 2010 guidelines (Schulz et al., 2010). |
| ScholarGateΣύνολο δεδομένων ↗ |
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