Blood test to predict postpartum depression in pregnant women

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to develop and validate a blood test that may predict postpartum depression (PPD) in pregnant women. Up to 500 participants will be recruited from the University of Virginia, focusing on those in their third trimester of pregnancy. The study will assess the accuracy of the test by determining the rates of true and false positives and negatives for PPD outcomes up to six months postpartum. Participants will not receive their individual test results, as the test is investigational and not yet FDA approved.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* subject must be pregnant (singleton pregnancy)
* \<30 weeks' gestation, age 18 or above
* able to provide written consent in English

Exclusion Criteria:

* The study team and/or PI may exclude anyone deemed unsafe to participate in the protocol.

Where it's running

• University of Virginia
  Charlottesville, Virginia, United States Recruiting
• Inova Health System
  Falls Church, Virginia, United States Recruiting

Study contacts

• Principal investigator: Jennifer L Payne, MD — University of Virginia
• Study coordinator: Meeta Pangtey, MPH
• Email: uwp7jh@uvahealth.org
• Phone: 434-987-7367

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.