Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Janssen Research & Development, LLC
Age
18–44
Sex
FEMALE
Healthy volunteers
Accepted
You may be eligible if
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
You may not be if
Participant is not English speaking
Lifetime mood disorder other than major depressive disorder (MDD) (example \[e.g.\], bipolar I) or anxiety 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
