Maternal Stress on Human Milk and Infant Outcomes

Recruiting N/A Interventional Study
Postpartum Depression Preterm Labor
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 – 50
Sex
Female
Study type
Interventional
Purpose
Prevention
Participants needed
500 (estimated)
Sponsor
University of Idaho · Other
Think this trial could be right for you?

Answer a few quick questions to see if you may meet the eligibility requirements.

Check Your Eligibility
About This Trial

The overarching purpose of this study is to determine if a modified 8-week mindfulness-based intervention (with a focus on self-compassion; MBSC) or 8 weeks of 2000 IU vitamin D supplementation will reduce stress and increase self-compassion in mothers of preterm infants and beneficially modify the human milk produced, and subsequently improve infant health.

Trial Locations
Loading…

Loading trial locations…

Eligibility Criteria
Inclusion Criteria: * Mothers of newborn infants at Kootenai Health NICU and the Palouse region Exclusion Criteria: \-
Contacts

Yimin Chen, PhD

2088857264

yiminc@uidaho.edu

CONTACT