Implementation of a Clinical Decision Support Tool for Postpartum Depression
NCT06818734
This study is recruiting at 3 US sites in 1 state, according to its ClinicalTrials.gov record last updated .
Summary
This study will evaluate the use of an automated process in the electronic health record (EHR) that will help providers to detect patients at risk of developing postpartum depression (PPD).
Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov
Conditions studied
- Postpartum Depression
Eligibility basics and study details
- Study type
- Interventional
- Phase
- Not applicable
- Ages
- 18 years and older
- Sex
- Female
- Healthy volunteers
- Accepted
- Sponsor
- Weill Medical College of Cornell University
- Last updated on ClinicalTrials.gov
- July 30, 2026
These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.
US recruiting sites
New York · 3
- Ob GYN Lower Manhattan 156 William street, New York City · New York, NY
- Weill Cornell Medicine OBGYN practice 72 street · New York, NY
- Weill Cornell Medicine- Women's Health practice 505 East 70th street, New York City · New York, NY
Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.