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Community-Partnered Doula Support for Neonatal Intensive Care Unit Families
Who can join
Ages 18 and older · Women
Full eligibility criteria
Inclusion Criteria: * baby admitted to NICU at Women and Infants Hospital * anticipated NICU stay greater than or equal to 2 weeks * English or Spanish speaking Exclusion Criteria: * Infant anticipated stay \< 2 weeks
About the study
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
What is being tested
- Enhanced doula support (behavioral)
Sponsor: Women and Infants Hospital of Rhode Island · Participants: 60 · Started: Mar 10, 2026
Contact the study team
- Alisse Hauspurg, MD · Phone: 401-274-1122
Official record on ClinicalTrials.gov — NCT07437131
Locations in the U.S.
| Rhode Island | Women and Infants Hospital, Providence |
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.