Prevention of Perinatal Depression Among At-risk Individuals Through Integration of a Multimedia, Web-based Intervention Within the Healthcare System

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
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

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: t
View:

• 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.

Locations
United States
Utah
University of Utah
RECRUITING
Salt Lake City
Contact Information
Primary
Gwen Latendresse, PhD CNM
gwen.latendresse@nurs.utah.edu
(801) 587-9636
Backup
Julie Neuberger, BS
julie.neuberger@nurs.utah.edu
801-587-3930
Time Frame
Start Date: 2023-04-04
Estimated Completion Date: 2025-12-30
Participants
Target number of participants: 120
Treatments
Other: Choice 1
Options; On-Demand (OD) alone or On-Demand (OD) with a facilitated discussion board (DB)
Other: Choice 2
Options:~On-Demand (OD) + Discussion board (DB) or OD + Video Conference (VC)
Other: Choice 3
Options; Om-Demand (OD) or On-Demand (OD) + Video Conference (VC)
Related Therapeutic Areas
Sponsors
Leads: University of Utah
Collaborators: National Institute of Nursing Research (NINR)

This content was sourced from clinicaltrials.gov

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