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Post-partum Care in the NICU (PeliCaN)

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University of Pennsylvania

Status

Completed

Conditions

Postpartum Period

Treatments

Other: Doula-coordinated, midwife-delivered postpartum care

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

This is a pilot randomized control trial to demonstrate the feasibility of a novel model of dyad-centered, doula-coordinated, midwife-delivered postpartum care located in the NICU in a large urban hospital.

Enrollment

37 patients

Sex

Female

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Preterm birth <34 weeks
  • Signed medical record release form

Exclusion criteria

  • Unable to read or sign informed consent
  • If the medical team believes that the infant may die or be transferred to another hospital in upcoming weeks
  • PI Discretion

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

37 participants in 2 patient groups

Doula Coordinated-Care Arm
Active Comparator group
Description:
Postpartum care will be doula-coordinated. The doula will meet with the mother at least once a week during their infant's NICU stay, with a minimum of 3 meetings. Participants will be given the option of seeing the study nurse midwife or their own provider. If the participant opts to see the nurse midwife, they can meet in a private office located in the NICU. The doula, as typical of the doula role, will coordinate any needed community services in the transition to home.
Treatment:
Other: Doula-coordinated, midwife-delivered postpartum care
Standard Postpartum Care Arm
No Intervention group
Description:
In this arm participants will receive usual postpartum care. They will be discharged from the hospital while their baby is still in the NICU and a plan will be made to for follow-up with their provider as an outpatient at some point in the next 6 weeks. The study coordinator will provide the participant with a community postpartum resources list.

Trial contacts and locations

1

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Central trial contact

Niesha Darden; Heather Burris, MD

Data sourced from clinicaltrials.gov

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