Dear SPM-experts,
We are going to run an event-related fMRI study with different kinds of
trials mixed together, and want to determine what arrangement of trials
will give us the greatest sensitivity to see separate activation for
different kinds of trials. (this is not a question about orthogonality,
we know how to do that)
How does one assess the sensitivity or effectiveness of a trial sequence?
Any ideas are highly appreciated.
Thank you,
Doerte
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