Maternal Mindfulness to Prevent Depression and Reduce Postpartum Pain (MaMiDaPP) Intervention
Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY
This phase I clinical trial tests the feasibility and safety of a self-guided, mobile mindfulness-based intervention to reduce post-cesarean pain and prevent postpartum depression.
Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Maximum Age: 45
Healthy Volunteers: t
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⁃ Women must self-identify as Latina/Latinx/Hispanic, Asian, African American, or non-Hispanic White.
⁃ Scheduled to undergo a planned cesarean delivery.
⁃ Be of 18-45 years of age
⁃ Have a singleton pregnancy
⁃ Score between 5 and 13 on the Edinburgh Postnatal Depression Scale (EPDS)
⁃ A history of depression
⁃ Have no chronic pain condition (e.g., fibromyalgia)
⁃ Own a computer, smartphone, or tablet
⁃ Have a reliable internet access to complete the online surveys.
• Be proficient in English or Spanish.
Locations
United States
Illinois
University of Illinois Urbana-Champaign
RECRUITING
Champaign
Contact Information
Primary
Sandraluz Lara-Cinisomo, Ph.D.
laracini@illinois.edu
217-300-3512
Time Frame
Start Date: 2025-12-01
Estimated Completion Date: 2028-03-31
Participants
Target number of participants: 75
Treatments
Experimental: Mindfulness
Receiving mobile, self-guided mindfulness intervention
No_intervention: Treatment as usual with monitoring
Receiving treatment as usual with monitoring by study PI and investigators.
Related Therapeutic Areas
Sponsors
Collaborators: Arrowhead Regional Medical Center, University of Utah, Southern Illinois University
Leads: University of Illinois at Urbana-Champaign