Implementation of a Clinical Decision Support Tool for Postpartum Depression

Part of paid clinical trials in Brooklyn, New York.

Sponsor
Weill Medical College of Cornell University
Study ID
NCT06818734
Status
Not Yet Recruiting

Notify me when recruiting opens

Save your spot on the interest list for this study. We'll keep your details with this study so our team can follow up when recruiting opens.

Not yet recruiting

Add your contact details and location so we can keep your interest tied to this study.

Conditions

  • Postpartum Depression

Eligibility Criteria

Sex
FEMALE
Age
18 Years - N/A
Healthy Volunteers
Accepted

Interventions

  • Clinical Decision Support Tool — OTHER
    The CDS in and AI algorithm that will alert clinicians only if patients have high risk of developing PPD, and provide clinicians with risk score, risk factors, and anticipatory actions with an order set to assist with ordering. Clinicians will make the ultimate clinical judgement after receiving CDS aid, including taking no actions towards PPD prevention. Clinicians will manage patients per usual care, including initiating PPD prevention 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.

Study Details

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).

Key Dates

Start date
May 1, 2026
Status verified
Mar 2026
Primary completion
Dec 1, 2026
Completion
Dec 1, 2026

Study Design

Enrollment
160 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE

Arms

  • Experimental: Intervention: CDS support , clinician
    Clinicians in the intervention arm will refer patients based on the CDS.The CDS will alert clinicians only if patients have high risk of developing PPD, and provide clinicians with risk score, risk factors, and anticipatory actions with an order set to assist with ordering. Clinicians will make the ultimate clinical judgement after receiving CDS aid, including taking no actions towards PPD prevention. 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.
  • No Intervention: No intervention: Patients
    The CDS will alert clinicians only if patients have high risk of developing PPD. 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.
  • Experimental: Intervention: Patients

Primary Outcome Measure

Acceptability as measured by Unified Theory of Technology Acceptance Theory (UTAUT). [ Time Frame: One month after initiation of tool use and three months after use. ]

Central Contacts

Locations (3)

FacilityCityStateZIPSite coordinators
Center for Community Health: 515 6th street (3rd floor)BrooklynNew York11215
Tracy Grossman, MD
[email protected]
Jessica Miller
718-499-2273
Tracy Grossman, MD (SUB_INVESTIGATOR)
Ob GYN Lower Manhattan 156 William street, New York CityNew YorkNew York10038
Szilvia Nagy, MD
[email protected]
Szilvia Nagy, MD (SUB_INVESTIGATOR)
Weill Cornell Medicine- Women's Health practice 505 East 70th street, New York CityNew YorkNew York10065
Rochelle Joly, MD
[email protected]
Rochelle Joly, MD (SUB_INVESTIGATOR)

Find similar trials in Brooklyn, NY

By research site
Center for Community Health: 515 6th street (3rd floor)· Brooklyn, NYOb GYN Lower Manhattan 156 William street, New York City· New York, NYWeill Cornell Medicine- Women's Health practice 505 East 70th street, New York City· New York, NY

Related Studies