RECRUITING

Postpartum Care in the NICU (PeliCaN) Transitions

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

This is a randomized controlled trial of a dyad-centered, doula support and healthcare coordination model of care in a large urban neonatal intensive care unit (NICU), which serves a high-risk, low-income, majority Black population. In addition to doula support and coordination of care in the NICU, there will be a warm handoff to a community doula to continue the support once infants leave the Hospital of the University of Pennsylvania (HUP) NICU.

Official Title

Postpartum Care in the NICU (PeliCaN) Transitions

Quick Facts

Study Start:2024-09-11
Study Completion:2027-08
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06521398

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:16 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:No
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * HUP postpartum patients who are at least 16 years old at the time their newborns' birth
  2. * Infant born at HUP
  3. * Preterm birth \<34 weeks
  4. * English language speaking
  1. * Unable to read or sign informed consent
  2. * Parents of infants transferred into HUP NICU
  3. * If the medical team believes that the infant may not live or be transferred to another hospital in upcoming weeks
  4. * HUP postpartum patients who are less than 16 years of age at the time of their newborns' birth

Contacts and Locations

Study Contact

Heather Burris, MD MPH
CONTACT
(215) 573-4916
Burrish@chop.edu
Niesha Darden
CONTACT
dardenn2@chop.edu

Principal Investigator

Heather Burris, MD MPH
PRINCIPAL_INVESTIGATOR
University of Pennsylvania

Study Locations (Sites)

Hospital of the University of Pennsylvania
Philadelphia, Pennsylvania, 19104
United States

Collaborators and Investigators

Sponsor: University of Pennsylvania

  • Heather Burris, MD MPH, PRINCIPAL_INVESTIGATOR, University of Pennsylvania

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 Date2024-09-11
Study Completion Date2027-08

Study Record Updates

Study Start Date2024-09-11
Study Completion Date2027-08

Terms related to this study

Additional Relevant MeSH Terms

  • Stress Disorders, Post-Traumatic
  • Premature Birth
  • Postpartum Depression
  • Postpartum Anxiety