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सिमुलेशन-सहायता प्राप्त पुष्टिकारी अनुसंधान×यादृच्छिक नियंत्रित परीक्षण (RCT)×
क्षेत्रअनुसंधान अभिकल्पप्रयोगात्मक अभिकल्प
परिवारProcess / pipelineHypothesis test
उद्भव वर्ष1980s–2000s (widespread integration in behavioral and social sciences)1948
प्रवर्तकNo single originator; tradition formalized through Monte Carlo methods (Metropolis & Ulam, 1949) applied to confirmatory designsJames Lind (early precursor, 1747); modern formulation: Austin Bradford Hill & Medical Research Council (1948)
प्रकारQuantitative hybrid designInterventional comparative study
मौलिक स्रोतMorey, R. D., Chambers, C. D., Aitken, M. R. F., Harris, C. R., Hoekstra, R., Lakens, D., Lewandowsky, S., Morey, C. C., Newman, D. P., Schonbrodt, F. D., Vanpaemel, W., Wagenmakers, E. J., & Zwaan, R. A. (2022). The Peer Reviewers' Openness Initiative: Incentivising open research practices through peer review. Royal Society Open Science, 3(1), 150547. link ↗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 ↗
उपनामsimulation-based confirmatory design, Monte Carlo confirmatory research, computational confirmatory study, simulation-enhanced hypothesis testingRCT, randomised controlled trial, clinical trial, Randomize Kontrollü Çalışma (RCT) Tasarımı
संबंधित57
सारांशSimulation-assisted confirmatory research integrates computational simulation — most commonly Monte Carlo methods — into a hypothesis-driven, confirmatory study design. Before or alongside empirical data collection, the researcher runs simulated data under specified model assumptions to establish expected parameter distributions, verify statistical power, and anticipate the behavior of the chosen analysis. The empirical findings are then evaluated against those simulation-derived benchmarks, strengthening the evidential value of confirmatory conclusions.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).
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