Optimizing Clinical Screening and Management of Maternal Mental Health: Predicting Women at Risk for Perinatal Depression

Inclusion Criteria:

- Participants must be English-speaking and able to understand and follow
clinician/researcher/provider recommendations

- Participants must be able to read and comprehend written communications (English) and
physically able to complete electronic patient-reported outcome (ePRO) assessments

- Participants must have access to a personal smartphone or a computer and an active
personal email address for which they are willing to use for data collection

- Each participant must sign an informed consent form (ICF) indicating that she
understands the purpose of and procedures required for this study and is willing to
participate in and comply with all procedures in the study

- Participant must be willing and able to have blood draws and to complete the
self-reported assessments via mobile electronic device during the study

Exclusion Criteria:

- Participant is not English speaking

- Lifetime mood disorder other than major depressive disorder (MDD) (example [e.g.],
bipolar I) or anxiety disorder

- Lifetime psychotic disorder (eg, schizophrenia, schizoaffective disorder)

- Lifetime alcohol or illicit substance dependence (moderate-severe)

- Current Post-traumatic Stress Disorder (PTSD), significant alcohol or illicit drug use
(Ethanol [ETOH]/nonprescription drug use) within 12 months greater than or equal to
(>=)occasional use