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This approach was based on promising results of a preceding trial in relapsed and refractory AML and a pilot study in previously untreated patients.
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A surprising imperative stimulus on the preceding trial resulted in a similar decrease of CSE (thumb, −0.24 mV/bit; little finger, −0.19 mV/bit; see Figure 3A).
Models with other predictors, e.g., RT on the preceding trial (an autoregressive effect), were not identifiable.
These results demonstrate that in high-confidence R3 trials subjects can detect a single-photon irrespective of the presence of a single photon in the preceding trial.
We isolated these responses by comparing activation during reversal trials (Treversal), with an unexpected outcome, with the preceding trial (Treversal − 1) where outcomes are fully expected.
In addition, the pattern presented in a current trial is independent of its preceding trial, in contrast to the serial-choice RT tasks.
This means that, following implementation of an innovation, possible efficiency gains are assumed to accumulate at a constant rate, as found in the preceding trial or modeling study.
Because of the slow BOLD response, in an event-related design activity in a current trial can be influenced by activation evoked by the preceding trial.
Participants were asked to determine as accurately as possible whether a left-pointing or right-pointing prime was presented in the preceding trial.
The opposing effect of the type of preceding trial was isolated by the contrast StroopINC>StroopCON taken to a 2nd level comparison between groups.
A new stimulus was presented 3 s after the end of the preceding trial.
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