Tests a mindfulness app for pain and low mood after childbirth
Tests a self-guided phone mindfulness program in adults after cesarean delivery.
Plain-language title generated from the registry record
Registry title: Maternal Mindfulness: Depression and Postpartum Pain
Key facts
- Where
- Champaign, United StatesSee the site
Could this be for you?
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you between 18 and 45 years old?
Source: NCT05400382, who can take part
Where in United States
- University of Illinois Urbana-ChampaignChampaign, United StatesTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- University of Illinois at Urbana-Champaign
- Trial code
- NCT05400382
- Record updated
- 6 August 2026
- Original description
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.Read full original descriptionShow less
Maternal Mindfulness to Prevent Depression and Reduce Postpartum Pain (MaMiDaPP) Intervention
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.
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.