Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
NCT06877104

Healing at Home 2.0 - Enhanced Chat Tool for Lowering Postpartum Depression

Led by University of Pennsylvania · Updated on 2026-03-27

156

Participants Needed

1

Research Sites

85 weeks

Total Duration

On this page

Sponsors

U

University of Pennsylvania

Lead Sponsor

M

March of Dimes

Collaborating Sponsor

AI-Summary

What this Trial Is About

The purpose of the study is to determine if access to a text-message based holistic chatbot support program "Healing at Home 2.0" decreases depressive symptoms as measured by the Edinburgh Postnatal Depression Scale (EPDS) compared to usual postpartum care for patients of color.

CONDITIONS

Official Title

Healing at Home 2.0 - Enhanced Chat Tool for Lowering Postpartum Depression

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Postpartum patients who have delivered a singleton baby at or after 37 weeks 0 days at the Hospital of the University of Pennsylvania
  • Self-identify as a person of color (non-White race confirmed with patient)
  • Able to speak, read, and write English
  • Age 18 years or older
  • Received prenatal care at outpatient practice affiliated with the Hospital of the University of Pennsylvania
  • Completed clinically administered Edinburgh Postnatal Depression Scale during inpatient stay
  • Routine discharge timing: day 2 or more after vaginal delivery, day 3 or more after cesarean delivery
Not Eligible

You will not qualify if you...

  • Unable to provide informed consent
  • Baby not discharged with mother at postpartum discharge
  • Does not have access to a mobile phone

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Hospital of the University of Pennsylvania

Philadelphia, Pennsylvania, United States, 19104

Actively Recruiting

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Research Team

M

Meaghan G McCabe, MPH

CONTACT

A

Angelina Malenda

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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