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Maternal Mindfulness: Depression and Postpartum Pain

NCT05400382 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 75

Last updated 2026-08-06

No results posted yet for this study

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.

Conditions

  • Depression, Unipolar
  • Pain, Postoperative

Interventions

BEHAVIORAL

Mindfulness

Meditation training to help reduce stress and reactivity to pain and other stressors.

Sponsors & Collaborators

  • Southern Illinois University

    collaborator OTHER

  • Arrowhead Regional Medical Center

    collaborator OTHER

  • University of Utah

    collaborator OTHER

  • University of Illinois at Urbana-Champaign

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-12-01
Primary Completion
2028-03-31
Completion
2028-03-31

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05400382 on ClinicalTrials.gov