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NCT05795114 · ClinicalTrials.gov registry record · NA

Perinatal Depression and Adverse Childhood Experiences: Prevention Trial

A NA study of Perinatal Depression, sponsored by Northwestern University.

Recruiting
Registry status
NA
Development phase
76
Enrollment target
1
Study location

NCT05795114 is a NA study of Perinatal Depression that is actively recruiting participants, run by Northwestern University. The registered enrollment target is 76 participants, below the 473-participant average among 12 other Perinatal Depression trials with a reported enrollment target (84% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05795114, a NA study of Perinatal Depression, is actively recruiting participants, sponsored by Northwestern University.

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

Study Summary

The goal of this clinical trial is to evaluate the impact of ROSE in individuals with adverse childhood experiences. The main question it aims to answer is, compared to enhanced treatment as usual, does the delivery of ROSE within a collaborative care model improve depressive symptom trajectories and prevent the development of perinatal depression. Participants will be randomized to either enhanced treatment as usual or the ROSE intervention, delivered by a care manager within a perinatal collaborative care program. They will complete self-reported surveys of their depression symptoms every 4 weeks to inform their symptom trajectories. They will also complete clinical interviews to establish any incident diagnoses of a major depressive episode.

Conditions Studied

Interventions

  • BEHAVIORAL Reach Out, Stand Strong, Essentials for New Mothers (ROSE) Program

Study Locations (1)

Illinois

  • Northwestern Medicine - Chicago

Trial Details

FieldValue
Enrollment Target 76 participants
Start Date 2023-07-20
Est. Completion 2026-01-31
Phase NA

Sponsor

Northwestern University

1,209 total trials

What the Registry Record Tells You About NCT05795114

The ClinicalTrials.gov registry entry for NCT05795114 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 76 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 473-participant average among 12 other Perinatal Depression trials with a reported enrollment target (84% lower). The listed sponsor is Northwestern University, which has 1,209 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Perinatal Depression appearing as the primary indexed condition, and to 1 intervention - of which Reach Out, Stand Strong, Essentials for New Mothers (ROSE) Program is the first listed.

NCT05795114 reports 1 study location spanning 1 distinct geographic area - top geographies include Illinois.

Frequently Asked Questions

What is clinical trial NCT05795114 about?

NCT05795114 is a clinical study titled "Perinatal Depression and Adverse Childhood Experiences: Prevention Trial". The goal of this clinical trial is to evaluate the impact of ROSE in individuals with adverse childhood experiences. The main question it aims to answer is, compared to enhanced treatment as usual, does the delivery of ROSE within a collaborative care model improve depressive symptom trajectories an...

What is the current status of trial NCT05795114?

This trial is currently recruiting. It is a NA study. The enrollment target is 76 participants. The study started on 2023-07-20. Estimated completion is 2026-01-31.

What conditions does trial NCT05795114 study?

This clinical trial studies the following conditions: Perinatal Depression.

What interventions are being tested in trial NCT05795114?

The interventions under investigation include: Reach Out, Stand Strong, Essentials for New Mothers (ROSE) Program (BEHAVIORAL).

Who is sponsoring clinical trial NCT05795114?

This trial is sponsored by Northwestern University, which has 1,209 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05795114 being conducted?

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

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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