You can have perfect lab techniques, beautiful R code, preregistration on OSF, and 10,000 citations…
But if you chose the wrong experimental design at the beginning, your entire study is scientific garbage wearing a lab coat.
Yet every year, thousands of MSc/PhD students and early-career researchers pick the wrong design — not because they are stupid, but because nobody taught them better.
Here are the 7 most common (and most dangerous) mistakes I see today — and how to fix them before you waste two years and a lots of money.
Mistake 1 – “CRD is fine, the field looks uniform”
Reality: No field is ever uniform.
New researchers love Completely Randomized Design because it’s simple in SPSS.
Result: soil fertility gradients, drainage patterns, and border effects inflate error terms → you miss real treatment differences → negative result → “nothing worked”.
Fix: Always start with Randomized Complete Block Design (RCBD) in the field. Block along the obvious gradient (slope, soil color, previous yield map). Only use CRD in pots on the same greenhouse bench.
Mistake 2 – Calling everything with a control group an “experiment”
Reality: If you didn’t randomize, it’s not an experiment.
I still see theses titled “Effect of X on Y” using alternation, hospital arrival order, or farmer’s choice as “randomization”. That’s quasi-experimental at best — and usually just observational with extra steps.
Fix: If true randomization is impossible, be honest: call it quasi-experimental, use difference-in-differences or propensity score matching, and stop claiming causality in the title.
Mistake 3 – Using between-subjects when within-subjects is obviously better
Reality: You need 4× more participants/plots to detect the same effect.
Example: testing three fertilizer rates on maize yield → most new researchers give each plot only one rate.
Correct: apply all three rates to the same plot in different years (with proper rotation) or use split-plot in space.
Fix: Ask: “Can the experimental unit receive more than one treatment?” If yes → repeated measures, crossover, or split-plot.
Mistake 4 – Split-plot layout but RCBD analysis
Reality: The single most common fatal error in agronomy theses today.
Irrigation or tillage as whole-plot, varieties as sub-plot → data analyzed as RCBD → irrigation effect looks significant at p<0.001 even when it’s noise.
Fix: Learn the two error terms rule. Whole-plot factor → tested against whole-plot error. Everything else → tested against sub-plot error. One wrong line in your code = rejected paper.
Mistake 5 – “I have 100 genotypes, so I’ll just use RCBD with 3 reps”
Reality: You now have 300 tiny plots and massive experimental error.
Alpha-lattice, row-column, or augmented designs exist for exactly this situation.
Fix: 40+ genotypes → switch to incomplete block designs. The agricolae package in R makes it painless.
Mistake 6 – Ignoring the hard-to-change factor
Reality: You want to test irrigation × variety × fertilizer.
You make 4×6×5 = 120 tiny plots and try to randomize everything → irrigation ends up with zero true replication.
Fix: Hard-to-change factors (irrigation, tillage, temperature, grazing) always go to the largest plot level (whole-plot, strip-plot, or whole-block).
Mistake 7 – Thinking preregistration fixes bad design
Reality: Preregistering a terrible design just gives you a time-stamped terrible design.
Open Science fixed p-hacking, not bad methodology.
Fix: Preregister the design justification too. Ask yourself: “Which specific threats to internal validity does my design control — and which ones does it leave open?”
The 30-Second Rule for Choosing the Right Design
Before you write your proposal, answer these four questions:
Write the answers on a sticky note. If your design doesn’t match the answers, change the design.
Final Truth
Drop your research question in the comments — I’ll tell you the correct design in one sentence.
PHD Success, Guaranteed.
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