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One-Stop baby visit may boost breastfeeding success

NCT ID NCT06395168

Symptom relief Sponsor: Mayo Clinic Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing This study
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tests whether combining a baby's first checkup after leaving the hospital with a lactation consultation helps more mothers breastfeed longer. About 246 mothers who plan to breastfeed will either get the combined visit or separate visits. Researchers will track breastfeeding rates at several points up to 12 months after birth.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Combined Newborn and Lactation Visit
What this could lead to
If it works, this could show that a single combined appointment makes it easier for new mothers to start and keep breastfeeding.
What could go wrong
This is a small, early study at one health system, so results may not apply everywhere. It only looks at breastfeeding rates, not other health outcomes.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 246 people

The number the study aims to enrol. It can still change while the study runs.

Started

Aug 2024

Expected to finish

Oct 2026

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Female participants only

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

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

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Conditions

The condition(s) this trial relates to.

Breast Feeding

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Breast feeding

Contacts and locations

Locations

  • Mayo Clinic Health System-Eau Claire Clinic

    Eau Claire, Wisconsin, 54703, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.