NCT05795114
Perinatal Depression and Adverse Childhood Experiences: Prevention Trial
Active, Not Recruiting
NAAges 18+InterventionalPreventionNorthwestern UniversityInvestigator-initiated
~76 participants
Updated 2026-07-22 on ClinicalTrials.gov
What's tested:Reach Out, Stand Strong, Essentials for New Mothers (ROSE) Program
At a glance
Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Depression symptoms
Measured over Up to 6 months postpartum
+1 more outcome measured
Conditions
Where it's being run
1 sites across 1 statesIllinois1
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
Do you actually qualify for this trial?
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Eligibility criteria
Inclusion
Age ≥ 18 years
At least one prenatal visit at Northwestern Medicine
Less than 24 weeks gestation
Non-anomalous pregnancy
English- or Spanish- speaking
ACE score ≥ 2
Singleton gestation
Exclusion
Intent to delivery outside of Prentice Women's Hospital
Active major depressive episode
Active substance use disorder
Participation in a study with a competing intervention or outcome
What this trial measures
- Depression symptomsUp to 6 months postpartum
Depression symptom trajectories will be measured via Patient Health Questionnaire-9 (PHQ-9) screens administered
- Perinatal depressionUp to 6 months postpartum
Perinatal depression includes any categorical diagnosis of a major depressive episode, assessed using the Longitudinal Interval Follow-Up Examination measured by trained research personnel masked to the intervention