Implementation of a Clinical Decision Support Tool for Postpartum Depression
Weill Medical College of Cornell University · NCT06818734
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · Women only
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 160
- US sites recruiting
- 3
- Study start
- July 1, 2026
- Record last updated
- July 30, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
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).
Being studied: Clinical Decision Support Tool
Conditions: Postpartum Depression
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- 18 years or older
- being seen at one of participating clinics
- pregnancy at 20 week gestation or more
Exclusion Criteria
- Does not speak inclusion
- does not have internet access
Clinician eligibility
- If they manage patients in the three clinics as a board-certified OBGYN clinician.
- No exclusion criteria apply for clinician based on their knowledge and experience in treating PPD
Recruiting US locations
Ob GYN Lower Manhattan 156 William street, New York City
New York, NY 10038
Site contact: Szilvia Nagy, MD · szn3001@med.cornell.edu
Weill Cornell Medicine OBGYN practice 72 street
New York, NY 10065
Site contact: Allison Boester, MD
Weill Cornell Medicine- Women's Health practice 505 East 70th street, New York City
New York, NY 10065
Site contact: Rochelle Joly, MD · roj9069@med.cornell.edu
Study contacts (from the official record)
- Rochelle Joly, MD · 646-962-4222 · roj9069@med.cornell.edu
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