JayUtah
Penultimate Amazing
You're skewing the test results in your favor by limiting participants to four sentences/answers. On top on that, you're giving them them the answers to choose from.
This is not ostensibly a problem. In the classic Zener card deck, for example, the participants have to choose from a small, well-defined set of drawn figures--five figures, five of each in a deck of 25. Later we can go down the rabbit hole of all the ways one could cheat at Zener guessing. But those aside, it's a valid test. The question is simply whether the guesses statistically fit an expected distribution. Having a finite set of possible outcomes allows us to create that model. Your suggestion does that too.
Having given the example of the Zener deck, I want to shift to a simpler protocol using a different variable. A typical Zener run does have a well-defined statistical basis, but it's a poor example for trying to explain the concept. It's not intuitive. So I'll pick one that is.
Consider instead a fair six-sided die. A single trial is a single fair throw of the die. The conductor throws the die, and visualizes the result. Separately, out of sight, the participant tries to guess which number came up on the die. In the single trial, the null hypothesis says the participant should guess correctly 1 out of every six times. Or rather, that the naked probability of a correct guess is p = 1/6.
But to test properly in statistics, we need a distribution. So we define a run as 60 trials. The score for that run is the number of times the participant correctly guessed the die number. In theory it will be 10 if the null holds. But in practice, even under the null, the scores from a series of runs will form a normal distribution around 10. Getting to that normal distribution is what's important.
We could define a run as 6 (cluster around 1), or as 600 trials (cluster around 100). The former gives us too few degrees of freedom. The distribution will cluster around 1, but since the numbers in the vicinity are 0, 1, and 2, it will be hard to see whether the actual experimental distribution fits the curve or not. 600 (clustered around 100) will let the data vary a lot more smoothly, but would probably be onerous for the participant. So let's say 60.
But we need more than one run. We might end up doing a large number of total trials, but they could be, say, 20 runs of 60 trials each. That gives us 20 data points for this participant. Then we try to fit the experimental data to a standard normal distribution with a mean of 10. If the result is p < 0.05 that the correctly parameterized normal curve can still explain the experimental data, then we will have shown a scientifically significant effect.1
We won't have proven ESP. We will simply have shown that there is an effect that we can then study further. Michel isn't even to that stage. With proper controls in place, and a defensible (if simplistic) statistical model, he can't show that there is an effect. Without an effect to explain, it's meaningless to think about any possible cause.
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1 But in this case the effect we're interested in is a shift in the μ > 10 direction. A shift in the other direction would possibly indicate a problem in the protocol. This is the correct way to diagnose methodology problems by looking at the results, not navel-gazing at subjective "credibility."