RECRUITING

Development of the Couplet Care Bassinet

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

The goal of this study is to evaluate the impact of the Couplet Care bassinet on maternal-infant outcomes in the postnatal hospital setting. The main question this study aims to answer is: Does the Couplet Care bassinet have better maternal-infant outcomes compared to the standard bassinet? The mother participants will: -be surveyed about experiences with and use of the bassinet including: the mother's sleep, breastfeeding, calls to staff, infant location, and satisfaction. Charts will be reviewed for additional outcomes. Hospital staff and administrators will be surveyed about experiences with the bassinet.

Official Title

Development of the Couplet Care Bassinet to Support Safe Implementation of Skin-to-skin Contact and rooming-in on Postnatal Units

Quick Facts

Study Start:2025-01-09
Study Completion:2025-07-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06533449

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. * postpartum female participant
  2. * at least 18 years of age
  3. * who can communicate in English
  1. * If postpartum female has had multiple infants (twins or more) or
  2. * participant has an infant who is not rooming-in, such as for infant or maternal intensive care

Contacts and Locations

Study Contact

Cecilia Tomori, PhD
CONTACT
2404416153
ctomori1@jh.edu
Monica Brown, MS
CONTACT
667-306-9823
mbrow374@jh.edu

Principal Investigator

Cecilia Tomori, PhD
PRINCIPAL_INVESTIGATOR
Johns Hopkins University

Study Locations (Sites)

Johns Hopkins Hospital
Baltimore, Maryland, 21287
United States

Collaborators and Investigators

Sponsor: Johns Hopkins University

  • Cecilia Tomori, PhD, PRINCIPAL_INVESTIGATOR, Johns Hopkins 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 Date2025-01-09
Study Completion Date2025-07-30

Study Record Updates

Study Start Date2025-01-09
Study Completion Date2025-07-30

Terms related to this study

Keywords Provided by Researchers

  • skin-to-skin
  • rooming-in
  • breastfeeding
  • sleep
  • bassinet
  • Cesarean Section

Additional Relevant MeSH Terms

  • Breastfeeding
  • Sleep
  • Patient Satisfaction