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Soothing sore breasts before birth may boost breastfeeding success

NCT ID NCT05796284

Symptom relief Sponsor: National Defense Medical Center, Taiwan 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
Running, but no longer taking on new participants.
Completed This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at whether a simple intervention to relieve breast tenderness in late pregnancy could improve breastfeeding, reduce breast engorgement, and lower stress for new mothers. Researchers followed 160 healthy pregnant women from 36 weeks onward. The goal was to see if easing discomfort before birth helps mothers feel more confident and less stressed after delivery.

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

160 people

The number who actually took part.

Started

Aug 2023

Finished

Jul 2024

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

20 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: * 1\. Healthy pregnant women over 20 years old, without mental illness, and the number of pregnancy weeks has reached 36 weeks; 2. Full term production; 3. Literate or able to communicate in Chinese and Taiwanese; 4. After explaining, agree to participate in the research, sign the consent form, and accept long-term follower Exclusion Criteria: 1. Pregnant women with a history of smoking, alcohol, and drug abuse; 2. Pregnant women have mental illness; 3. Maternal complications during childbirth or postpartum, such as: postpartum hemorrhage, infection, etc.; 4. Newborns with congenital abnormalities and major diseases; 5. Pregnant women who are unable or unwilling to breastfeed due to illness or other factors; 6. Refuse to accept breast compression intervention will be excluded from participating in the study

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Conditions

The condition(s) this trial relates to.

Breast Feeding pregnancy disorder

As listed by the trial registrant

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

Breastfeeding Efficacy, self Pregnancy related

Contacts and locations

Locations

  • National defense medical center

    Taipei, Taiwan, 114201, Taiwan

More trials for these conditions

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