Implementation of a Clinical Decision Support Tool for Postpartum Depression
Start Date
7/1/2026
Completion Date
12/1/2026
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).
Detailed Description
The goal of this randomized clinical trial is to assess the implementation of a clinical decision support (CDS) tool. The tool is designed to assist providers in managing patients at risk of developing of postpartum depression. Investigators hypothesize that this tool will be acceptable and feasible for use and improve the use of mental health services for postpartum depression. Patients in the control arm will receive usual care, while those in the intervention arm will receive CDS. Clinicians will manage patients per usual care, including initiating PPD preventive such as conducting referrals to nutrition and behavioral health, suggest educational readings through patient portals, or no actions. Clinicians in the intervention arm will refer patients based on the CDS.
Eligibility Criteria
Age Range: 18 years to No maximum
Interventions
Clinical Decision Support Tool
Conditions
Locations
Center for Community Health: 515 6th street (3rd floor)
Brooklyn, New York 11215
United States
Ob GYN Lower Manhattan 156 William street, New York City
New York, New York 10038
United States
Weill Cornell Medicine OBGYN practice 72 street
New York, New York 10065
United States
Weill Cornell Medicine- Women's Health practice 505 East 70th street, New York City
New York, New York 10065
United States