Improving access to mental health support for pregnant and postpartum women
Official title: Prevention of Perinatal Depression Among At-risk Individuals Through Integration of a Multimedia, Web-based Intervention Within the Healthcare System
Run by University of Utah · NCT06049433 · Data updated 2026-11-12
This study is testing a new online mental health support program for pregnant and new moms who might be at risk for postpartum depression to see how well it works for different people.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | Women only |
| Enrollment | 120 (estimated) |
| Sponsor | University of Utah Academic / other |
| Locations | 1 site (Salt Lake City, Utah) |
| Status | Recruiting |
| Started | April 4, 2023 |
| Main results expected | August 30, 2025 |
| Study ends | December 30, 2025 |
| Registry record updated | December 6, 2024 |
| Trial ID | NCT06049433 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include pregnant or postpartum women aged 18 and older who are at risk for perinatal depression and speak English or Spanish.
✕Probably not a fit
Patients with serious mental illnesses, substance use disorders, or severe anxiety may not benefit from this intervention.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This project aims to evaluate and refine the implementation of a digital mental health intervention for postpartum depression among at-risk pregnant and postpartum women from diverse backgrounds. The study will enroll 120 participants using a randomized preference design to assess the impact of sociocultural factors on engagement and symptom trajectory. By integrating the intervention within existing maternal clinical care settings, the research seeks to optimize the feasibility and acceptability of the approach, ultimately preparing for larger multisite trials. The implementation strategies will be informed by input from key stakeholders and a Community Advisory Board throughout the project.
Why it matters
Potential benefit: If successful, this intervention could significantly improve mental health outcomes for pregnant and postpartum women at risk for depression.
How similar studies have gone: Other studies have shown promise in using digital mental health interventions for postpartum depression, indicating potential for success in this approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * 18+ years of age, who at the time of screening * Have a viable pregnancy or are postpartum (up to 1 year) * Identified as at-risk for PD (any one of the following: * EPDS score equal to or greater than 9 or less than 21 * History of depression/anxiety * 2 or more significant life events) * English- or Spanish-speaking * Currently attending a UHealth clinic or rural public health partner clinic. Exclusion Criteria: * Have a substance use disorder * Current diagnosis of serious mental illness, such as psychosis, schizophrenia, bipolar disorder, severe depression (including EPDS \> 20) * Severe anxiety, suicidality, or currently taking any medications for a mental health condition.
Where it's running
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University of Utah
Salt Lake City, Utah, United States Recruiting
Study contacts
- Principal investigator: Gwen Latendresse — University of Utah
- Study coordinator: Gwen Latendresse, PhD CNM
- Email: gwen.latendresse@nurs.utah.edu
- Phone: (801) 587-9636
Similar studies
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A pilot program tests a Parents and Babies intervention to see if it’s feasible, acceptable, and potentially helpful for LGBTQ+ people who are pregnant or within a year postpartum and have mild depressive symptoms.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.