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NCT06521398 · ClinicalTrials.gov registry record · NA

Postpartum Care in the NICU (PeliCaN) Transitions

A NA study of Stress Disorders, Post-Traumatic and Postpartum Depression, sponsored by University of Pennsylvania.

Recruiting
Registry status
NA
Development phase
20
Enrollment target
1
Study location

NCT06521398: Recruiting NA study of Stress Disorders, Post-Traumatic and Postpartum Depression, sponsored by University of Pennsylvania.

NCT06521398 is a NA study of Stress Disorders, Post-Traumatic and Postpartum Depression that is actively recruiting participants, run by University of Pennsylvania. The registered enrollment target is 20 participants, below the 156-participant average among 66 other Stress Disorders, Post-Traumatic trials with a reported enrollment target (87% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06521398, a NA study of Stress Disorders, Post-Traumatic and Postpartum Depression, is actively recruiting participants, sponsored by University of Pennsylvania.

RECRUITING
Registry status
NA
Development phase
20 participants
Enrollment target
1
Study location

Study Summary

This is a randomized controlled trial of a dyad-centered, doula support and healthcare coordination model of care in a large urban neonatal intensive care unit (NICU), which serves a high-risk, low-income, majority Black population. In addition to doula support and coordination of care in the NICU, there will be a warm handoff to a community doula to continue the support once infants leave the Hospital of the University of Pennsylvania (HUP) NICU.

Primary Outcome

This will measured by the PTSD Checklist for DSM-5 (PCL-5) is a 20-item self-report measure that assesses the 20 DSM-5 symptoms of PTSD. The symptom severity score ranges from 0-80 with 80 being a worse score.

Interventions

  • OTHER Doula Support

Study Locations (1)

Pennsylvania

  • Hospital of the University of Pennsylvania - Philadelphia

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2024-09-11
Est. Completion 2027-08
Phase NA
University of Pennsylvania

1,423 total trials

What NCT06521398 shows while recruiting

NCT06521398 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 156-participant average among 66 other Stress Disorders, Post-Traumatic trials with a reported enrollment target (87% lower).

The record links to 4 conditions, with Stress Disorders, Post-Traumatic appearing as the primary indexed condition, and to 1 intervention - of which Doula Support is the first listed.

NCT06521398 reports a single indexed study location in Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT06521398 about?

NCT06521398 is a clinical study titled "Postpartum Care in the NICU (PeliCaN) Transitions". This is a randomized controlled trial of a dyad-centered, doula support and healthcare coordination model of care in a large urban neonatal intensive care unit (NICU), which serves a high-risk, low-income, majority Black population. In addition to doula support and coordination of care in the NICU, ...

What is the current status of trial NCT06521398?

This trial is currently recruiting. It is a NA study. The enrollment target is 20 participants. The study started on 2024-09-11. Estimated completion is 2027-08.

What conditions does trial NCT06521398 study?

This clinical trial studies the following conditions: Stress Disorders, Post-Traumatic, Postpartum Depression, Premature Birth, Postpartum Anxiety.

What interventions are being tested in trial NCT06521398?

The interventions under investigation include: Doula Support (OTHER).

Who is sponsoring clinical trial NCT06521398?

This trial is sponsored by University of Pennsylvania, which has 1,423 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06521398 being conducted?

This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Stress Disorders, Post-Traumatic

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06521398's enrollment target sits among peer trials

20 61st of 66 higher than 6 of 66 other Stress Disorders, Post-Traumatic trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Stress Disorders, Post-Traumatic trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06521398, the US trial registry maintained by the National Library of Medicine. NCT06521398 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.