Implementation of a Clinical Decision Support Tool for Postpartum Depression
Recruiting · NCT06818734 · Interventional (participants receive a specific treatment) · Lead sponsor: Weill Medical College of Cornell University
View the official record on ClinicalTrials.gov →Interventions studied
Clinical Decision Support Tool
What this trial is about
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 take part
Age range
18 Years and older
Sex
Female
Healthy volunteers
Yes - healthy volunteers may be accepted
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
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
Where it is running
4 locations listed across 1 US state.
- Center for Community Health: 515 6th street (3rd floor) - Brooklyn, New York, United States
- Ob GYN Lower Manhattan 156 William street, New York City - New York, New York, United States
- Weill Cornell Medicine OBGYN practice 72 street - New York, New York, United States
- Weill Cornell Medicine- Women's Health practice 505 East 70th street, New York City - New York, New York, United States