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OpenTrials
Completed

NCT Number: NCT06533449

Development of the Couplet Care Bassinet

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.

Completed

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Johns Hopkins Hospital

Baltimore, Maryland, 21287, United States

About this study

The current study is a Phase II evaluation of the Couplet Care bassinet, designed by Couplet Care Limited Liability Corporation (LLC), a novel infant clinical bassinet designed to support safe implementation of skin-to-skin contact and rooming-in on postnatal units. Until recently, the standard of hospital care for healthy term newborns was to be observed and cared for by maternity staff in a nursery with other infants. However, as detailed in the World Health Organization (WHO) / United Nations International Children's Emergency Fund (UNICEF) report Ten Steps for Successful Breastfeeding, it is now recommended that mothers and infants "room-in" together 24 hours per day, with one hour of separation allowable for procedures outside of the postnatal unit room. As a result, the practice of nursery care is no longer recommended nor facilitated. However, most bassinets in United States (U.S.) hospitals are still designed for use by ambulatory nursery staff, rather than by mobility-impaired new mothers. Current bassinets were not designed for patient use and restrict maternal access to the infants and introduce infants to increased risk of physical injury. Bassinet tubs can tip under the weight of mothers' arms and the height of the tub walls can compromise infant handling. Often, new mothers are required to either substantially twist the body to access the infant or get up out of bed to reach the infant, despite being in immediate postpartum period and needing to heal. Such actions can cause new mothers to experience unnecessary frustration, pain, or even injury. This is especially critical to the one-third of U.S. women who deliver by cesarean section, as the mother's limited ability to move and postpartum pain hinder timely and safe infant care, undermine breastfeeding, impede the mother's own recovery, and contribute to risk of infant falls and suffocation. The substantial difficulty maneuvering infants in and out of conventional bassinets, coupled with the pain and fatigue felt by new mothers, increase the risk of 1) infant drops, and 2) falling asleep with infants in unsafe arrangements. To address these gaps in safety Couplet Care has developed a novel bassinet that allows mothers to position infants over the mother's bed and handle the infants independently.

To ensure usability and safety, the Couplet Care bassinet design incorporates (1) a lower tub wall with access points, making it easier for a mother to reach her infant, (2) adjustability features that allow for bassinet positioning over the mother, and (3) a design that secures the tub into the frame.

In this phase of the project, the researchers will build on insights of Phase I to refine Couplet Care bassinet design, so it is manufacturable and compliant with Food and Drug Administration (FDA) regulations. Next, the Study Team component of the study will:

  • Evaluate the impact of the Couplet Care bassinet on maternal-infant patient outcomes in a powered randomized controlled trial (RCT)
  • Evaluate the usability and adoptability of the device from clinician perspectives. Successful accomplishment of this Phase II effort will position the Couplet Care bassinet for commercialization, delivering a bassinet that promotes safe mother-infant connection during rooming-in, while reducing the risk of infant drops/falls and suffocation, maternal waking from unmet infant needs, and demands on nurses for assistance for non-medical needs.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

(from protocol)

  • postpartum female participant
  • at least 18 years of age
  • who can communicate in English

Exclusion criteria

  • If postpartum female has had multiple infants (twins or more) or
  • participant has an infant who is not rooming-in, such as for infant or maternal intensive care

Treatment and study plan

Couplet Care Bassinet

Device

Couplet Care Bassinet

Standard Bassinet

Device

Standard Bassinet

Primary outcomes

  1. Maternal reported infant wakings

    Time frame: Up to 3 days (until discharge)

    Number of times mothers report infant waking

Secondary outcomes

  1. Post-Partum pain levels

    Time frame: Up to 3 days (until discharge)

    reported pain level from participants to medical staff on a scale of 1-10. Higher score indicates higher pain.

  2. Infant feeding substance

    Time frame: Up to 3 days (until discharge)

    Type of feeding substance (participant's own milk, donor human milk, formula use, combination)

  3. Length of postpartum hospitalization

    Time frame: Up to 3 days (until discharge)

    Length of hospitalization

  4. Number of minutes infants were outside of the post-natal unit

    Time frame: Up to 3 days (until discharge)

    Number of minutes infants were outside of the post-natal unit (rooming-in)

  5. Breastfeeding frequency

    Time frame: Up to 3 days (until discharge)

    Breastfeeding frequency

  6. Breastfeeding duration (minutes)

    Time frame: Up to 3 days (until discharge)

    Breastfeeding duration

  7. Number of calls to clinical staff

    Time frame: Up to 3 days (until discharge)

    number of calls by study participants to clinical staff

Other outcomes

  1. Clinician usability assessment

    Time frame: 1 year

    Clinician usability assessment table; clinician must rate 13 statements regarding usability of the bassinet on a scale of 1 to 5 in which 1 is "strongly disagree" and 5 is "strongly agree." Score range 13-65; higher score higher usability

  2. Administrator adoptability assessment

    Time frame: 1 year

    Adoptability table in which administrators rate 4 statements regarding adoptability of the bassinet on a scale of 1 to 5 with 1 being "strongly disagree" and 5 being "strongly agree." Score range 4-20,higher score higher adoptability.

  3. Satisfaction with Bassinet Design

    Time frame: 1 year

    Participants, clinicians, and administrators will be provided open ended questionnaires regarding the design of the bassinet and satisfaction with bassinet use. The participants will be asked two questions to rate the bassinet on ease of use and design on a scale of 1 to 10 with 1 being "not at all" and 10 being "very much". Score range 2-20.

Sponsors and collaborators

Lead sponsor

Johns Hopkins University

Other

Collaborators

  • Couplet Care LLC
  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Registry information

Official study title

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

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Aug 1, 2024
Registry last updated
Jun 5, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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