Healing At Home 2.0 - Enhanced Chat Tool for Lowering Postpartum Depression
Purpose
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
- Depression, Postpartum
- Postpartum Care
Eligibility
- Eligible Ages
- Over 18 Years
- Eligible Genders
- Female
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- Postpartum patients who have delivered a singleton baby at or after 37w0d at the Hospital of the University of Pennsylvania - Self-identify as a person of color (listed on chart as non-White race and confirmed with patient) - Able to speak, read and write English - Age ≥18 - Prenatal care at outpatient practice affiliated with the Hospital of the University of Pennsylvania - Completion of clinically administered EPDS during inpatient stay - Routine discharge timing, day 2 or more after vaginal delivery, day 3 or more after cesarean delivery
Exclusion Criteria
- Unable to provide informed consent - Baby not discharged with mother at postpartum discharge - Does not have access to a mobile phone
Study Design
- Phase
- N/A
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel Assignment
- Primary Purpose
- Supportive Care
- Masking
- None (Open Label)
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
|
No Intervention Standard of care |
Routine postpartum care. |
|
|
Experimental Healing @ Home Program (H@H 2.0) |
Routine postpartum care and the use of an algorithm-based text message support program for six weeks. |
|
Recruiting Locations
More Details
- Status
- Recruiting
- Sponsor
- University of Pennsylvania
Detailed Description
Healing at Home (H@H) 2.0 is a comprehensive technology-based postpartum support program which provides 24/7 support to individuals through use of an SMS chatbot for six weeks postpartum. This will be a randomized controlled trial (RCT) with an intervention arm consisting of patients who are planning to be discharged at routine timing (as determined by their clinical team) with access to H@H 2.0 postpartum SMS chatbot platform and a control arm which consists of usual postpartum care.
