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 — OTHER
    The 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 intervention
    Participants 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

Locations (2)

FacilityCityStateZIPSite coordinators
NewYork-Prebyterian/Weill Cornell Medical CenterNew YorkNew York10065
Natalie Benda
Robin Kalish
NewYork-Presbyterian Columbia University Irving Medical CenterNew YorkNew York10032
Natalie Benda
Natalie Benda, PhD (PRINCIPAL_INVESTIGATOR)

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