Actively Recruiting
More Time More Milk - Wearable, Wireless Breast Pumps to Increase Accessibility of Milk Expression for NICU Mothers
Led by University of Texas at Austin · Updated on 2024-12-09
30
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating the impact of wearable, wireless breast pumps on how often and how much milk mothers of premature infants can express. This randomized controlled crossover trial focuses on mothers whose infants were born at or before 29 weeks and 6 days of gestation. The study aims to compare milk expression frequency and volume using wearable pumps versus standard hospital-grade pumps to improve milk accessibility for NICU mothers. Participants will use a wearable, wireless breast pump in addition to their usual hospital pump. The study follows a crossover design where mothers receive the wearable pump with lactation specialist support either during the first or second week, with the other week using standard care. This allows comparison between the two methods over two consecutive weeks. Mothers will be monitored for the number of pumping sessions and volume of milk expressed over seven days in each study period. Researchers will collect data on milk volume, percentage of required volume pumped, and pumping frequency. The study involves support from lactation specialists and aims to assess how the wearable pump affects milk expression in real-life settings such as cuddling the baby or performing daily activities.
CONDITIONS
Brief Title
A Randomized Controlled Trial of Impact of Wearable, Wireless Breast Pumps on Frequency and Efficacy of Milk Expression in Mothers of Premature Infants
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Mother of infant born at 29 weeks and 6 days gestation or earlier
- Mother still pumping milk at 4 weeks after birth
You will not qualify if you...
- Current use of mother's own wearable breast pump
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 week per intervention period
Participants use a wearable, wireless breast pump in addition to their usual hospital grade pump, with support from a lactation specialist during the assigned week.
Weekly visits for up to 2 weeks
Duration - 1 week per intervention period
Participants use standard hospital grade breast pumps without the wearable wireless pump during the assigned week.
Weekly visits for up to 2 weeks
Trial Site Locations
Total: 1 location
1
Ascension Seton Medical Center
Austin, Texas, United States, 78705
Actively Recruiting
Research Team
E
Erica Ortiz
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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