taVNS-Paired Breastfeeding to Improve Breastfeeding at Discharge

Recruiting N/A Interventional Study
Premature Birth Breastfeeding, Exclusive Feeding; Difficult, Newborn
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
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At a Glance
Age
35 Weeks and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
10 (estimated)
Sponsor
Medical University of South Carolina · Other
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About This Trial
Investigators aim to improve the skills of premature or sick term infants in breastfeeding by boosting motor learning with transcutaneous vagus nerve stimulation. Investigators will recruit 10 premature, ≥ 35 weeks gestational age, or convalescing sick term infants admitted to the NICU at MUSC to participate in this study. Infants will receive taVNS treatments once a day with breastfeeding's for u…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Infants ≥ 35 weeks post-menstrual age, * Clinically stable, without significant respiratory support, * Deemed safe to breastfeed by OT/SLP/lactation, * Maternal interest in breastfeeding, * Are not breastfeeding well despite the assistance of a lactation consultant. Exclusion…
Contacts

Haley Burdge

8432144089

burdge@musc.edu

CONTACT

Dorothea Jenkins

jenkd@musc.edu

CONTACT