A Study of Pregnant and Postpartum Women With and Without Mood Disorders

NCT03615794 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 300

Last updated 2025-12-30

No results posted yet for this study

Summary

This study is looking at genetic, biological, and environmental causes and how all three may work together to cause postpartum mood episodes. Participants will have psychiatric histories taken and will be monitored throughout pregnancy and during the postpartum period for the development of depressive or other mood episodes. Biological measures, including hormone levels, immunological measures, and growth factors will be collected. Environmental factors such as sleep deprivation and stress will also be measured. These factors will be considered in the setting of genetic and epigenetic data with the hope that investigators will ultimately be able to predict the onset of postpartum mood episodes in this vulnerable population.

Conditions

Sponsors & Collaborators

Principal Investigators

  • Jennifer Payne, MD · University of Virginia

  • Richard Lee · Johns Hopkins University

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-10-01
Primary Completion
2024-01-31
Completion
2024-05-06

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03615794 on ClinicalTrials.gov