Protocol for Pilot Study on Self-Management of Depressive Symptoms in Pregnancy.

Nurs Res

Patricia A. Kinser, PhD, WHNP-BC, RN, FNAP, FAAN, is Associate Professor, Virginia Commonwealth University School of Nursing, Richmond. Sara Moyer, RN, is Research Assistant, Virginia Commonwealth University School of Nursing, Richmond. Suzanne Mazzeo, PhD, is Professor, Department of Psychology, Virginia Commonwealth University School of Nursing, Richmond. Timothy P. York, PhD, is Associate Professor, Virginia Commonwealth University School of Medicine, Richmond. Ananda Amstadter, PhD, is Associate Professor, Virginia Commonwealth University School of Medicine, Richmond. Leroy Thacker, PhD, is Associate Professor, Virginia Commonwealth University Department of Biostatistics, Richmond. Angela Starkweather, PhD, ACNP-BC, CNRN, RN, FAAN, is Professor, University of Connecticut College of Nursing, Storrs.

Published: April 2020

AI Article Synopsis

  • Pregnant women experiencing depressive symptoms need effective, non-drug therapies to improve their well-being and reduce symptoms during and after pregnancy.
  • The "Mindful Moms" pilot study aims to test a 12-week self-management intervention for 40 pregnant women, focusing on its feasibility and preliminary effects on mental health.
  • The study will also explore how participation may influence DNA methylation patterns associated with depression, providing insights for future research in non-pharmaceutical treatment options.

Article Abstract

Background: Pregnant women with depressive symptoms face significant treatment challenges and are in great need of safe, effective, accessible, inexpensive, and nonpharmacological self-management therapies to enhance well-being, reduce the burden of symptoms both during their pregnancy and postpartum, and prevent chronic sequelae.

Objectives: In this article, we describe the protocol for our pilot study testing a self-management intervention entitled, "Mindful Moms," designed to foster women's ability to address current depressive symptoms and enhance resilience to prevent recurrence.

Methods: We will conduct a longitudinal pilot trial of the 12-week intervention with pregnant women with depressive symptoms (n = 40); the primary aim is to determine the feasibility and acceptability of the intervention. The secondary aim is to examine preliminary effects of the intervention on maternal psychobehavioral outcomes in pregnancy and 6 weeks postpartum. The third aim will quantify genome-wide and gene-specific DNA methylation patterns associated with depressive symptoms during pregnancy and investigate whether intervention participation influences these patterns.

Results: This study is currently ongoing.

Discussion: Findings from this study will inform future research addressing the need for nonpharmacological self-management interventions for pregnant women with depressive symptoms.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6910977PMC
http://dx.doi.org/10.1097/NNR.0000000000000382DOI Listing

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