Table 2.
Group | Number of sessions | Total subjects | Finished trial | Subject that did not meet ongoing inclusion/exclusion criteria
|
Discomfort
|
||||
---|---|---|---|---|---|---|---|---|---|
Atypical headache or migraine
|
Atypical skin condition
|
||||||||
Between session | Within session | Between session | Within session | Between session | Within session | ||||
Sham-tDCS | 636 | 37 | 33 | 2 | 0 | 2 | 0 | 0 | 0 |
tDCS | 623 | 33 | 22 | 2 | 0 | 8 | 0 | 0 | 1 |
MHF-tPCS | 646 | 30 | 25 | 3 | 0 | 1 | 0 | 0 | 1 |
Total | 1905 | 100 | 80 | 7 | 0 | 11 | 0 | 0 | 2 |
Subjects who did not meet the ongoing inclusion/exclusion criteria were withdrawn for discomfort, atypical headache and atypical skin condition (see Methods). All other subjects were categorized as “finished trial”. Subjects elected how many sessions to complete over 6 weeks with the minimal requirement of completing four treatment sessions per seven days and a minimal enrollment commitment of 2 weeks.