Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
Healthy Volunteers
NCT06395168

Mayo Clinic Health System Northwest Wisconsin Integrated Maternal Postpartum Appointment Combination

Led by Mayo Clinic · Updated on 2025-12-08

246

Participants Needed

1

Research Sites

110 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this study is to explore whether combining the first post-hospital newborn provider visit and lactation consultation into a single appointment can enhance rates of successful breastfeeding initiation and continuation at predefined intervals (e.g., one week, one month, two months, three months, four months, six months, and 12 months postpartum).

CONDITIONS

Official Title

Mayo Clinic Health System Northwest Wisconsin Integrated Maternal Postpartum Appointment Combination

Who Can Participate

Age: 18Years +
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Mothers aged greater than or equal to 18 years
  • Mothers who can provide informed consent for participation
  • Mothers registered as patients at Mayo Clinic Health System Northwest Wisconsin
  • Mothers who have given birth within the past four days prior to enrollment
  • Mothers who intend to breastfeed their newborns
  • Mothers willing and able to participate in the study
  • Mothers able to communicate in English
  • Mothers with internet access to complete electronic data collection
Not Eligible

You will not qualify if you...

  • Mothers unable or unwilling to provide informed consent
  • Mothers younger than 18 years
  • Mothers unable to complete study procedures or follow-up visits
  • Mothers with medical complications interfering with breastfeeding (e.g., breast reduction)
  • Mothers with no intention to breastfeed their newborns
  • Mothers unwilling to follow up with lactation
  • Infants who have already had their first postpartum outpatient provider visit
  • Pre-term infants (less than 37 weeks gestation)
  • Infants admitted to special care for more than two days
  • Length of stay or expected stay greater than four days
  • Transfer to an outside facility
  • Mothers unable to communicate in English
  • When study slots are no longer available

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Mayo Clinic Health System-Eau Claire Clinic

Eau Claire, Wisconsin, United States, 54703

Actively Recruiting

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Research Team

L

Linh Tran

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

2

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