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NCT06049433 · ClinicalTrials.gov registry record · NA
Maternal Mental Health Access - MaMa
A NA study of Postpartum Depression and Perinatal Depression, sponsored by University of Utah.
- Recruiting
- Registry status
- NA
- Development phase
- 120
- Enrollment target
- 1
- Study location
NCT06049433: Recruiting NA study of Postpartum Depression and Perinatal Depression, sponsored by University of Utah.
NCT06049433 is a NA study of Postpartum Depression and Perinatal Depression that is actively recruiting participants, run by University of Utah. The registered enrollment target is 120 participants, below the 473-participant average among 47 other Postpartum Depression trials with a reported enrollment target (75% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06049433, a NA study of Postpartum Depression and Perinatal Depression, is actively recruiting participants, sponsored by University of Utah.
- RECRUITING
- Registry status
- NA
- Development phase
- 120 participants
- Enrollment target
- 1
- Study location
Study Summary
This hybrid effectiveness-implementation project will allow the team to evaluate and refine implementation in preparation for future multisite trials to ultimately move the Evidence-Based Intervention (EBI) to scale among diverse populations. The plan is to enroll 120 at-risk pregnant and postpartum women from rural, urban, and Latino populations. Using a randomized preference design to also evaluate patient and sociocultural factors in participation and symptom trajectory. Using the Implementation Research Logic Model, the team will evaluate the implementation feasibility and acceptability of a remote-access and on-demand MBCT PD prevention intervention that is integrated within maternal clinical care settings using an existing patient portal. Successful achievement of the study aims will result in a refined implementation protocol for future studies that are sufficiently powered to evaluate the effectiveness of an integrated Digital Mental Health Technology and to estimate the cost/benefit ratio
Primary Outcome
EPDS Scores are between 0 and 30, with scores 13 and above indicating depressive illness, or a high risk of developing a depressive disorder. Using scores that are between 9-20 Qualitative; semi structured interview Quantitative; patient satisfaction survey, number of referrals for at-risk patients, patients registering on YoMingo. focus groups, individual interviews, questionnaires
Conditions Studied
Interventions
- BEHAVIORAL Maternal Mental Health Access for Postpartum Depression- Prevention and UPLIFT- intervention
- BEHAVIORAL On-Demand + Discussion board (DB)
- BEHAVIORAL Arm 2
- BEHAVIORAL On Demand (OD) + Video Conference (VC)
- BEHAVIORAL Arm 3
Study Locations (1)
Utah
- University of Utah - Salt Lake City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 120 participants |
| Start Date | 2023-04-04 |
| Est. Completion | 2025-12-30 |
| Phase | NA |
What NCT06049433 shows while recruiting
NCT06049433 is an interventional study that assigns participants to a tested intervention. The registered 120 participants enrollment target is mid-sized for trials with a published cap, below the 473-participant average among 47 other Postpartum Depression trials with a reported enrollment target (75% lower).
The record links to 2 conditions, with Postpartum Depression appearing as the primary indexed condition, and to 5 interventions - of which Maternal Mental Health Access for Postpartum Depression- Prevention and UPLIFT- intervention is the first listed.
NCT06049433 reports a single indexed study location in Utah.
Frequently Asked Questions
What is clinical trial NCT06049433 about?
NCT06049433 is a clinical study titled "Maternal Mental Health Access - MaMa". This hybrid effectiveness-implementation project will allow the team to evaluate and refine implementation in preparation for future multisite trials to ultimately move the Evidence-Based Intervention (EBI) to scale among diverse populations. The plan is to enroll 120 at-risk pregnant and postpartum...
What is the current status of trial NCT06049433?
This trial is currently recruiting. It is a NA study. The enrollment target is 120 participants. The study started on 2023-04-04. Estimated completion is 2025-12-30.
What conditions does trial NCT06049433 study?
This clinical trial studies the following conditions: Postpartum Depression, Perinatal Depression.
What interventions are being tested in trial NCT06049433?
The interventions under investigation include: Maternal Mental Health Access for Postpartum Depression- Prevention and UPLIFT- intervention (BEHAVIORAL), On-Demand + Discussion board (DB) (BEHAVIORAL), Arm 2 (BEHAVIORAL), On Demand (OD) + Video Conference (VC) (BEHAVIORAL), Arm 3 (BEHAVIORAL).
Who is sponsoring clinical trial NCT06049433?
This trial is sponsored by University of Utah, which has 818 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06049433 being conducted?
This trial has 1 study location across Utah. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Postpartum Depression
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 NCT06049433's enrollment target sits among peer trials
120 22nd of 47 higher than 26 of 47 other Postpartum Depression trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Postpartum Depression 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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