Actively Recruiting

Phase Not Applicable
FEMALE
ID06723067

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

FEMALE

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Implementation

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

Implementation

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

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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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