> Is it possible to combine these two techniques to first control for RT across all trials, and then extract the per-trial estimates?
Emilie, the question is very confusing... When using -stim_times_IM, you basically estimate the response at each trial. Now if you want to further control for RT across trials, do you mean that you want to estimate the response at each trial while pretending the RT each each trial is fixed at the *average* (or some other constant) RT value?
Gang