Maternal Mental Health Access - MaMa (NCT06049433)
Prevention of Perinatal Depression Among At-risk Individuals Through Integration of a Multimedia, Web-based Intervention Within the Healthcare System
🩺 Plain-English Summary (8th-Grade Level)
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
Who can join: Review the eligibility criteria below.
Location: University of Utah — Salt Lake City, Utah
Age range: 18 Years
🧪 Interventions in This Study
- 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)
- On Demand (OD) + Video Conference (VC) (BEHAVIORAL)
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (1 Sites)
- University of Utah — Salt Lake City, Utah
📞 Contact the Study Coordinator
Phone: (801) 587-9636
Email: gwen.latendresse@nurs.utah.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Postpartum Depression
- Preventing Postpartum Depression in Immigrant Latinas — Baltimore, Maryland
- Public Health Nurse-Peer Co-Led Group Cognitive Behavioral Therapy for Postpartum Depression — Hamilton, Ontario
- The Safety, Tolerability, and Effectiveness of Quetiapine in Postpartum Depression — London, Ontario
- The Maternal Well-Being Study — Amarillo, Texas
- CBT for Postpartum Depression and Infant Emotion Regulation — Hamilton, Ontario
- Whole-Body Hyperthermia for Mood and Anxiety Disorders — New York, New York
Explore by condition: All Postpartum Depression clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.