Clinical trial Recruiting at 1 site Interventional Ages 18 and up Women only

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.

More Postpartum Depression trials

Quick facts

Study typeInterventional
Ages18 Years and up
SexWomen only
Enrollment120 (estimated)
SponsorUniversity of Utah
Academic / other
Locations1 site (Salt Lake City, Utah)
StatusRecruiting
StartedApril 4, 2023
Main results expectedAugust 30, 2025
Study endsDecember 30, 2025
Registry record updatedDecember 6, 2024
Trial IDNCT06049433 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

  • University of Utah
    Salt Lake City, Utah, United States
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.