Ignite Creation Date:
2025-12-25 @ 2:21 AM
Ignite Modification Date:
2026-01-25 @ 5:08 AM
Study NCT ID:
NCT06818734
Status:
NOT_YET_RECRUITING
Last Update Posted:
2025-11-24
First Post:
2025-02-07
Is Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Implementation of a Clinical Decision Support Tool for Postpartum Depression
Sponsor:
Weill Medical College of Cornell University
Organization:
Study Overview
Official Title:
Implementation of a Clinical Decision Support Tool for Postpartum Depression
Status:
NOT_YET_RECRUITING
Status Verified Date:
2025-11
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
CDS
Brief 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.
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.
Study Oversight
Has Oversight DMC:
False
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?: