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एबीएबी क्रॉसओवर डिज़ाइन×मल्टीपल बेसलाइन डिज़ाइन×यादृच्छिक नियंत्रित परीक्षण (RCT)×
क्षेत्रप्रयोगात्मक अभिकल्पप्रयोगात्मक अभिकल्पप्रयोगात्मक अभिकल्प
परिवारProcess / pipelineProcess / pipelineHypothesis test
उद्भव वर्ष1960s–1970s19681948
प्रवर्तकMurray Sidman and colleagues in applied behavior analysisDonald M. Baer, Montrose M. Wolf, Todd R. RisleyJames Lind (early precursor, 1747); modern formulation: Austin Bradford Hill & Medical Research Council (1948)
प्रकारSingle-subject experimental designSingle-subject experimental designInterventional comparative study
मौलिक स्रोतBarlow, D. H., Nock, M. K., & Hersen, M. (2009). Single Case Experimental Designs: Strategies for Studying Behavior Change (3rd ed.). Pearson. ISBN: 978-0205474929Baer, D. M., Wolf, M. M., & Risley, T. R. (1968). Some current dimensions of applied behavior analysis. Journal of Applied Behavior Analysis, 1(1), 91–97. 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 ↗
उपनामABAB reversal design, reversal design, withdrawal design, ABAB single-subject designMBD, multiple-baseline single-case design, staggered baseline design, multiple-probe designRCT, randomised controlled trial, clinical trial, Randomize Kontrollü Çalışma (RCT) Tasarımı
संबंधित247
सारांशThe crossover ABAB design is a single-subject experimental design that alternates between baseline (A) and intervention (B) conditions twice within the same participant. By withdrawing and reintroducing the treatment, the researcher can demonstrate experimental control: if behavior improves with B and reverts with A, the causal link between the intervention and the outcome is established without a separate control group.The multiple baseline design is a single-subject experimental design that demonstrates functional control by introducing an intervention at staggered time points across two or more baselines — typically across different behaviors, individuals, or settings. Because no withdrawal of treatment is required, it is especially suitable when the target behavior is irreversible or when removing an effective intervention would be unethical.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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