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. 2023 Jun 29;14:1184998. doi: 10.3389/fneur.2023.1184998

Table 1.

Study design.

Screening Baseline Period 1 Outcome Wash-out period Period 2 End of study
Session 1 Session 2 Session 1 Session 2
Visit V1 V2 V3 ~ V6 V7 ~ V11 V11 2 weeks V12 ~ V16 V17 ~ V21 V22
ENROLLMENT
Informed consent V
Eligibility screen V V
Randomized allocation V
Taking a clinical photo V
MRI-based simulation and planning for tDCS V
INTERVENTIONS
Personalized tDCS Sham-tDCS V V V V V
ASSESSMENTS
Outcome variables V
Vital signs V V V V V V V V V
Physical examination V V
K-CRS-R V V V
EEG V V
NCS-R V V V V V V V V
MRI, fMRI, and PET scan V V
Other variables Adverse events V V V V V V V