Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
NCT07437131

Community-Partnered Doula Support for Neonatal Intensive Care Unit Families

Led by Women and Infants Hospital of Rhode Island · Updated on 2026-04-07

60

Participants Needed

1

Research Sites

38 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this clinical trial is to learn if pairing families who have a baby in the Neonatal Intensive Care Unit with a community doula improves stress. The main questions it aims to answer are: Researchers will compare stress levels among families with a baby in the neonatal intensive care unit who are paired with a community doula compared to those who receive standard care. Participants will: Complete baseline surveys and physical assessments (blood pressure and blood sample collection) and again after six weeks If they are randomized to receive doula support, they will meet with the doula weekly to receive additional parental support for six weeks

CONDITIONS

Official Title

Community-Partnered Doula Support for Neonatal Intensive Care Unit Families

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Baby admitted to NICU at Women and Infants Hospital
  • Anticipated NICU stay of 2 weeks or longer
  • English or Spanish speaking
Not Eligible

You will not qualify if you...

  • Infant expected to stay in NICU less than 2 weeks

AI-Screening

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Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Women and Infants Hospital

Providence, Rhode Island, United States, 02905

Actively Recruiting

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Research Team

A

Alisse Hauspurg, MD

CONTACT

S

Sarbattama Sen, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

2

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