Assessing the Maternal Outcome Monitoring Systems
Part of paid clinical trials in New York, New York.
- Sponsor
- Columbia University
- Study ID
- NCT06415942
- Status
- Recruiting
Conditions
- Maternal Complication of Pregnancy
- Maternal Death
Eligibility Criteria
- Sex
- FEMALE
- Age
- 18 Years - N/A
- Healthy Volunteers
- Accepted
Interventions
- Maternal Outcome Monitoring and Support system — OTHERThe Maternal Outcome Monitoring and Support system is a mobile health application that allows participants to choose symptoms they may be having that are warning signs of pregnancy related death. They then receive decision support about when they should seek medical care (call their provider or go to an emergency room).
Study Details
Pregnancy-related death is a growing public health issues, which are of particular concern to minority groups, including African-Americans and Spanish-speaking Latinas. Our proposal aims to improve a patient's ability to detect warning signs of pregnancy related death and seek medical care.
Key Dates
- Start date
- Dec 11, 2024
- Status verified
- May 2026
- Primary completion
- Jan 31, 2027
- Completion
- Jan 31, 2027
Study Design
- Enrollment
- 80 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- OTHER
Arms
- Experimental: MOMS interventionParticipants in this condition will receive the MOMS symptom monitoring and decision support intervention. This is a single arm trial.
Primary Outcome Measure
Patient activation [ Time Frame: Baseline to 6 weeks postpartum ]
Central Contacts
- Natalie Benda917-426-3069
Locations (2)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| NewYork-Prebyterian/Weill Cornell Medical Center | New York | New York | 10065 | Natalie Benda Robin Kalish |
| NewYork-Presbyterian Columbia University Irving Medical Center | New York | New York | 10032 | Natalie Benda Natalie Benda, PhD (PRINCIPAL_INVESTIGATOR) |
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