Salīdzināt metodes
Apskatiet izvēlētās metodes blakus; rindas, kas atšķiras, ir izceltas.
| Divkārtējās aklo testu pirms- un pēcpārbaudes eksperimentālā dizains× | Randomizēts kontrolēts pētījums (RCT)× | |
|---|---|---|
| Nozare | Eksperimentu plānošana | Eksperimentu plānošana |
| Saime≠ | Process / pipeline | Hypothesis test |
| Izcelsmes gads≠ | Mid-20th century (combined form widely adopted 1960s onward) | 1948 |
| Autors≠ | Campbell & Stanley (formalized pretest-posttest design, 1963); double-blind blinding convention developed in clinical pharmacology (19th-20th century) | James Lind (early precursor, 1747); modern formulation: Austin Bradford Hill & Medical Research Council (1948) |
| Tips≠ | True experimental design | Interventional comparative study |
| Pirmavots≠ | Campbell, D. T., & Stanley, J. C. (1963). Experimental and quasi-experimental designs for research. In N. L. Gage (Ed.), Handbook of Research on Teaching (pp. 171-246). Rand McNally. 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 ↗ |
| Citi nosaukumi | DB-pretest-posttest design, double-blind pre-post design, masked pretest-posttest RCT, double-masked pre-post experiment | RCT, randomised controlled trial, clinical trial, Randomize Kontrollü Çalışma (RCT) Tasarımı |
| Saistītās≠ | 5 | 7 |
| Kopsavilkums≠ | The double-blind pretest-posttest experimental design is a true experiment in which participants are randomly assigned to treatment and control conditions, outcome data are collected both before and after the intervention, and neither participants nor outcome assessors know which condition each participant received. Combining baseline measurement with strong blinding, the design controls for both pre-existing group differences and expectancy-driven bias, making it a gold-standard approach in clinical and behavioral research. | 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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