Not Yet RecruitingNot Applicable

Implementation of a Clinical Decision Support Tool for Postpartum Depression

United States160 participantsStarted 2026-05-01

Plain-language 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).

Who can participate

Age range18 Years

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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

What they're measuring

Acceptability as measured by Unified Theory of Technology Acceptance Theory (UTAUT).

Timeframe: One month after initiation of tool use and three months after use.

Appropriateness as measured by Appropriateness Measure (IAM).

Timeframe: One month after initiation of tool use and three months after use.

Feasibility as measured by Feasibility of Intervention Measure (FIM).

Timeframe: One month after initiation of tool use and three months after use.

Mental Health service utilization as measured by number of mental health visits

Timeframe: one month and three month

Trial details

NCT IDNCT06818734

SponsorWeill Medical College of Cornell University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-12-01

Contact for this trial

Rochelle Joly, MD

646-962-4222 roj9069@med.cornell.edu

View on ClinicalTrials.gov More Postpartum Depression trials