Given that there is no documentation of whether the events during the hour of test time were more or less stressful than those before it, and no taking the time of day, diet and exercise, sleep, location (quiet island or next to a construction site), etc into account, the data seems useless.
As a note, I have no idea why he bothered trying to guess what he had taken. What possible value could that have in this type of experiment?
Perhaps the correct course of action would be to ask for feedback in the design phase of an N=1 trial, especially a longer one, to avoid some basic mistakes.
It gives a hint of how well the blinding worked.
> no documentation of whether the events during the hour of test time were more or less stressful than those before it, and no taking the time of day, diet and exercise, sleep, location
Assuming the blinded samples are uniformly randomly distributed, and assuming the study goes on long enough, then you'd expect that stuff to average out.
But I agree, it should be recorded nonetheless. That way you can verify at the end that it did, in fact, average out as you expected. If it didn't then your data is invalid.
That would not be a problem regarding the averaging I referred to, although it could well pose a problem for measurement depending on how it interacted with the selected metrics.
Note that the averaging I refer to is not regarding all possible values of some metric, but rather any discrepancy in the distribution of metrics which we expected to follow the same distribution between the sample and the control.
I think maybe there's a misunderstanding? It seems that we both agree that a variety of additional variable should be logged. I was not suggesting to omit them, but rather to use discrepancies in them to detect fundamental issues with the data or study design. I would also expect larger studies to do the same where possible.
At 94 data points it is entirely possible that there would be outliers that would have averaged out for a larger N but did not. In such a scenario the presence of such outliers should then be taken to indicate a problem with the data (ie the more discrepancies you observe, the less you should trust the data).
I of course agree that logging them is basic scientific methodology - in order to detect issues with the experiment, and even hopefully to see the signal through the noise.
>While I was blinded during each trial, I saw the theanine/D result when I wrote it down. Over time I couldn’t help but notice that my stress dropped even when I took vitamin D, and that I was terrible at predicting what I’d taken
That is not blinding