🏛️ Verified NIH Record • Updated 2026-07-28
Implementation of a Clinical Decision Support Tool for Postpartum Depression (NCT06818734)
🟢 Recruiting Observational / Diagnostic 📋 Clinical Research Protocol Sponsor: Weill Medical College of Cornell University
🩺 Plain-English Summary (8th-Grade Level)
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).
Who can join: Review the eligibility criteria below.
Location: Center for Community Health: 515 6th street (3rd floor) — Brooklyn, New York
Age range: 18 Years
🧪 Interventions in This Study
- Clinical Decision Support Tool (OTHER)
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (4 Sites)
- Center for Community Health: 515 6th street (3rd floor) — Brooklyn, New York
- Ob GYN Lower Manhattan 156 William street, New York City — New York, New York
- Weill Cornell Medicine OBGYN practice 72 street — New York, New York
- Weill Cornell Medicine- Women's Health practice 505 East 70th street, New York City — New York, New York
📞 Contact the Study Coordinator
Phone: (646) 962-4222
Email: roj9069@med.cornell.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Postpartum Depression
- Preventing Postpartum Depression in Immigrant Latinas — Baltimore, Maryland
- Public Health Nurse-Peer Co-Led Group Cognitive Behavioral Therapy for Postpartum Depression — Hamilton, Ontario
- The Safety, Tolerability, and Effectiveness of Quetiapine in Postpartum Depression — London, Ontario
- The Maternal Well-Being Study — Amarillo, Texas
- CBT for Postpartum Depression and Infant Emotion Regulation — Hamilton, Ontario
- Whole-Body Hyperthermia for Mood and Anxiety Disorders — New York, New York
Explore by condition: All Postpartum Depression clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.