השוואת שיטות
סקרו את השיטות שבחרתם זו לצד זו; שורות שבהן יש הבדל מודגשות.
| ניסוי פקטוריאלי עם סמיות יחידה× | ניסוי מבוקר אקראי חד-סמיות× | |
|---|---|---|
| תחום | תכנון ניסויים | תכנון ניסויים |
| משפחה | Process / pipeline | Process / pipeline |
| שנת המקור≠ | Factorial design: 1926; single-blinding as systematic practice: mid-20th century | 1948 (formalized); single-blind variant established in mid-20th century clinical trial methodology |
| הוגה השיטה≠ | Fisher, R. A. (factorial design); blinding practices formalized in clinical trials literature (20th century) | Bradford Hill and colleagues (MRC streptomycin trial, 1948); blinding conventions codified in CONSORT guidelines |
| סוג≠ | Controlled experimental design | Experimental design — blinded randomized trial |
| מקור מכונן≠ | Montgomery, D. C. (2017). Design and Analysis of Experiments (9th ed.). Wiley. ISBN: 978-1119113478 | Schulz, K. F., Altman, D. G., Moher, D., & CONSORT Group. (2010). CONSORT 2010 statement: Updated guidelines for reporting parallel group randomised trials. BMJ, 340, c332. DOI ↗ |
| כינויים≠ | single-masked factorial trial, single-blind factorial design, SB factorial experiment | single-masked RCT, single-blind RCT, single-blind trial, SB-RCT |
| קשורות | 5 | 5 |
| תקציר≠ | A single-blind factorial experiment combines factorial design — simultaneously varying two or more independent factors across all their level combinations — with single-blinding, in which participants are unaware of which treatment condition they have been assigned to while researchers and administrators remain unmasked. This design enables efficient estimation of main effects and interactions while reducing participant-side response bias. | A single-blind randomized controlled trial (SB-RCT) is a rigorous experimental design in which participants are randomly assigned to treatment or control conditions while remaining unaware of which condition they have received. Investigators, outcome assessors, and data analysts are not blinded. By masking participants, the design eliminates placebo and nocebo response biases on the participant side, while preserving investigator flexibility to administer and monitor the intervention. |
| ScholarGateמערך נתונים ↗ |
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