RECRUITING

Assessing the Maternal Outcome Monitoring Systems

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Single Arm Clinical Trial of a Novel Smartphone-based Somatic and Psychological Symptom Monitoring and Decision Support Tool for African American and Spanish Speaking Patients in the Near Postpartum Period

Quick Facts

Study Start:2024-12
Study Completion:2026-01-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06415942

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Greater than 28 weeks pregnant
  2. * Receiving healthcare in the United States
  3. * Age 18 years or older
  4. * \[Identify as Black or African American race AND able to speak and read English, AND preferred language of English\] OR \[Identify as Hispanic/Latino Ethnicity AND Spanish able to speak and read Spanish AND preferred language of Spanish\]
  5. * Planned delivery at the following NewYork-Presbyterian hospitals: Children's Hospital of New York, Allen Hospital, Weill Cornell Medical Center, Lower Manhattan Hospital
  1. * Severe cognitive impairment
  2. * Major psychiatric illness
  3. * Concomitant terminal illness that would preclude participation.

Contacts and Locations

Study Contact

Natalie Benda
CONTACT
917-426-3069
nb3115@cumc.columbia.edu

Study Locations (Sites)

NewYork-Presbyterian Columbia University Irving Medical Center
New York, New York, 10032
United States
NewYork-Prebyterian/Weill Cornell Medical Center
New York, New York, 10065
United States

Collaborators and Investigators

Sponsor: Columbia University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-12
Study Completion Date2026-01-31

Study Record Updates

Study Start Date2024-12
Study Completion Date2026-01-31

Terms related to this study

Keywords Provided by Researchers

  • pregnancy related death
  • patient reported outcomes
  • mHealth
  • patient activation

Additional Relevant MeSH Terms

  • Maternal Death
  • Maternal Complication of Pregnancy