Closed tjmahr closed 5 years ago
Hello! Thank you for bringing up this issue. I wanted to see if you could please provide some guidance. Were you able to resolve this issue? Which time did you end up using for further analysis? Thanks! Z
Ooops I think I used RTTime, but I read in both. My current code gazedata files is here https://github.com/tjmahr/littlelisteners/blob/master/R/gazedata.R
Today, I wondered if it would be possible to identify probable trial boundaries (Inter-Trial Intervals) from the time columns in gazedata files emitted by Eprime.
My first thought was to
diff(gazedata$RTTime)
to calculate the difference in time between Frame N and Frame N-1. The biggest jumps in time would be the ITIs. Which works perfectly:But on the plot, I see some weird diffs:
The first one shows up in the data as:
And the second as:
Clocks
The column
RTTime
is what we might call Eprime Local Time. I have used this column because stimulus presentation times in the Eprime administration log are measured with the same clock and relative time, making it easy to sync up Eprime's stimulus presentation with gaze location. RTTime is measured in milliseconds, possibly the running milliseconds from the start of the experiment:The gazedata file also provides a column for
TETTime
for Tobii Eye Tracker Time, which has none of these hiccups:But it's apparently measured as milliseconds since whenever computer time 0 was in the 70's
Questions
Some questions I need to figure out:
When I synchronize time using the Tobii clock, it kinda straightens those kinks. Plots below focus on the first set of weird points...