Actively Recruiting
Development of the Couplet Care Bassinet
Led by Johns Hopkins University · Updated on 2025-08-05
500
Participants Needed
1
Research Sites
81 weeks
Total Duration
On this page
Sponsors
J
Johns Hopkins University
Lead Sponsor
E
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Development of the Couplet Care Bassinet
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Postpartum female participant
- At least 18 years of age
- Able to communicate in English
You will not qualify if you...
- Postpartum female with multiple infants (twins or more)
- Infant not rooming-in, such as infant or maternal intensive care
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Johns Hopkins Hospital
Baltimore, Maryland, United States, 21287
Actively Recruiting
Research Team
C
Cecilia Tomori, PhD
CONTACT
M
Monica Brown, MS
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
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