Experiences with SSRIs During Pregnancy Please refer to this study by identifier 5365
Principal Investigator(s) Catherine Monk
Purpose
The purpose of this study is to learn about pregnant women’s moods and experiences, such as depression or taking anti–depressant medication, and if these experiences influence children’s development.
Type of Study: Observational Type Setting of Study: outpatient Clinical Trials.gov number: Providing Clinical Treatment?: No
Study Activities
Filling Out Forms Computer Tasks Psychophysiology measurements Provides Payment: Reimbursement for transportation Provides Payment: Compensation for study related procedures
Eligibility
Ages Eligible for Study: 18 Years - 40 Years Genders Eligible for Study: Female
This study is recruiting Healthy Volunteers.
Criteria
Inclusion Criteria: Healthy pregnancy
Taking SSRIs
English speaker
Location: Clinic: Division: Behavioral Medicine
Study chairs or principal investigators: Catherine Monk Ph.D., Principal Investigator
