Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT06818734

Implementation of a Clinical Decision Support Tool for Postpartum Depression

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
160 (estimated)
Sponsor
Weill Medical College of Cornell University · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Accepted

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.

Conditions

Interventions

TypeNameDescription
OTHERClinical Decision Support ToolThe 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.

Timeline

Start date
2026-05-01
Primary completion
2026-12-01
Completion
2026-12-01
First posted
2025-02-10
Last updated
2026-04-02

Locations

3 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT06818734. Inclusion in this directory is not an endorsement.