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The decision to offer a "full support admission" rather than a "PICU trial" (see below) has to result from a multidisciplinary discussion.
Within each block, one additional trial (a 'fixation' trial, see below) was pseudorandomly interleaved within the sequence of twelve trials.
Approval for the prospective interventional clinical trial (see below) was obtained from the IRB, the European Medicines Agency (EMEA, London, UK) and the German competent health authority (Paul-Ehrlich Institut, Berlin, Germany).
During each trial, the animal had to establish fixation within 200 ms of the fixation spot onset and maintain fixation within a ±0.5° window until the fixation spot was turned off toward the end of the trial (see below).
This strategy was posteriorly implemented in the CUPID trial (see below).
The six cameras were strategically positioned in the laboratory to ensure that all anatomical markers were captured throughout the trial (see below).
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Importantly, however, there was a relationship between working memory and the number of completed trials (see below).
Participants were informed that the feedback was not based on performance in trials without motion coherence (baseline trials, see below).
We were also able to include negative control groups of chickens in these experiments, which was not possible for the large-scale field trials (see below).
The direction of movement relative to the vibrating stake appeared to be random, and this was subsequently confirmed in a different set of trials (see below).
The CRs were first analysed for blocks 1 6 excluding the tone alone trials (see below).
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