เปรียบเทียบวิธี
ดูวิธีที่เลือกเทียบกันแบบเคียงข้าง แถวที่ต่างกันจะถูกเน้นไว้
| การออกแบบการทดลองแบบวัดก่อน-หลังการทดลองนำร่อง× | การทดลองสุ่มและมีกลุ่มควบคุม (Randomized Controlled Trial - RCT)× | |
|---|---|---|
| สาขาวิชา | การออกแบบการทดลอง | การออกแบบการทดลอง |
| ตระกูล≠ | Process / pipeline | Hypothesis test |
| ปีกำเนิด≠ | 1963 (formal codification by Campbell & Stanley); pilot trials widely used from mid-20th century onward | 1948 |
| ผู้ริเริ่ม≠ | Donald T. Campbell and Julian C. Stanley (experimental design codification); pilot study concept widely credited to early 20th-century clinical trial practice | James Lind (early precursor, 1747); modern formulation: Austin Bradford Hill & Medical Research Council (1948) |
| ประเภท≠ | Experimental / feasibility design | Interventional comparative study |
| แหล่งต้นตำรับ≠ | 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 ↗ |
| ชื่อเรียกอื่น | pilot pretest-posttest study, small-scale pretest-posttest trial, feasibility pretest-posttest design, pilot two-group pretest-posttest | RCT, randomised controlled trial, clinical trial, Randomize Kontrollü Çalışma (RCT) Tasarımı |
| ที่เกี่ยวข้อง≠ | 1 | 7 |
| สรุป≠ | A pilot pretest-posttest experimental design is a small-scale, preliminary study that applies a pretest-posttest measurement framework to a limited sample before a full-scale experiment. Its primary goals are to assess the feasibility of procedures, estimate effect sizes for power analysis, identify instrument problems, and uncover logistical barriers — all before committing to the cost and scale of a definitive trial. It combines the internal-validity advantages of repeated measurement with the pragmatic scope of a pilot study. | 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). |
| ScholarGateชุดข้อมูล ↗ |
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