RECRUITING

Mayo Clinic Health System Northwest Wisconsin Integrated Maternal Postpartum Appointment Combination

Conditions

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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).

Official Title

IMPAC: Integrated Maternal Postpartum Appointment Combination in Mayo Clinic Health System Northwest Wisconsin

Quick Facts

Study Start:2024-08-19
Study Completion:2025-12
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06395168

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Mothers aged greater than or equal to 18 years.
  2. * Mothers who are able to provide informed consent for participation in this study.
  3. * Mothers registered as patients at Mayo Clinic Health System Northwest Wisconsin.
  4. * Mothers who have given birth within the past four days prior to enrollment into this study.
  5. * Mothers who intend to breastfeed their newborns.
  6. * Mothers who are willing and able to participate in this study.
  7. * Mothers who are able to communicate in English.
  8. * Mothers with the ability to connect to the internet and complete electronic data collection.
  1. * Mothers who are unable or unwilling to provide informed consent for participation in this study.
  2. * Mothers less than 18 years of age.
  3. * Mothers unable to complete study procedures or follow-up visits.
  4. * Mothers with medical complications that could interfere with breastfeeding (e.g., breast reduction).
  5. * Mothers who have no intention to breastfeed their newborns.
  6. * Mothers who are unwilling to follow up with lactation.
  7. * Infants who have already had their first postpartum outpatient provider visit.
  8. * Pre-term infants (less than 37 weeks).
  9. * Special care admission greater than two days.
  10. * Length of stay or anticipated LOS greater than four days.
  11. * Transfer to an outside facility.
  12. * Inability to communicate in English.
  13. * When slots are no longer available.

Contacts and Locations

Principal Investigator

Karen Myhre
PRINCIPAL_INVESTIGATOR
Mayo Clinic

Study Locations (Sites)

Mayo Clinic Health System-Eau Claire Clinic
Eau Claire, Wisconsin, 54703
United States

Collaborators and Investigators

Sponsor: Mayo Clinic

  • Karen Myhre, PRINCIPAL_INVESTIGATOR, Mayo Clinic

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-08-19
Study Completion Date2025-12

Study Record Updates

Study Start Date2024-08-19
Study Completion Date2025-12

Terms related to this study

Additional Relevant MeSH Terms

  • Breast Feeding