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The purpose of the current study is to perform a unified, homogeneous data collection protocol that includes a large cohort of patients undergoing different treatment options for Major Depressive Disorder (MDD) as an avenue for investigating optimal biomarkers for depression treatments on an individual patient level.
Inclusion Criteria: Ketamine cohort * Adult between the ages of 18 - 65, inclusive at time of enrollment * Primary diagnosis of MDD as defined by DSM-5 * Determined by clinic to be eligible for ketamine treatment and agrees to receive ketamine treatment * Agrees to start ketamine treatment in conjunction with study participation to capture pre-treatment measurements accurately * Has not received a ketamine treatment course in the past 12 months * Has not received a TMS treatment course in the past 3 months * Ability to consent for themselves * Fluency in English (speaking and reading) SPRAV…
Kernel Flow2 measurements.