Health Trials

Implementation of a Clinical Decision Support Tool for Postpartum Depression

ConditionPostpartum Depression
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorWeill Medical College of Cornell University

About this trial

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).

Eligibility criteria

Qualifiers

18 years or older

being seen at one of participating clinics

pregnancy at 20 week gestation or more

Disqualifiers

Does not speak inclusion

does not have internet access

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

Trial design

Treatments tested in this trial

  • Clinical Decision Support Tool

Treatment groups

160 Participants
are divided into 3 treatment groups

Locations

3
Center for Community Health: 515 6th street (3rd floor)11215, BrooklynNew York, United States
Ob GYN Lower Manhattan 156 William street, New York City10038, New YorkNew York, United States
Weill Cornell Medicine- Women's Health practice 505 East 70th street, New York City10065, New YorkNew York, United States

Sponsors and collaborators

Weill Medical College of Cornell University

Lead sponsor

Source ClinicalTrials.gov