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Boosting breastfeeding confidence in teen moms: a new approach put to the test

NCT ID NCT07025265

Disease control Sponsor: Saglik Bilimleri Universitesi 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Aug 05, 2026 · Last updated Aug 06, 2026 · Updated 1 time

Summary

This trial tests a program designed to help adolescent mothers feel more confident about breastfeeding. The program includes two face-to-face education sessions, supportive text messages, a home visit after birth, and phone counseling. Researchers will measure changes in breastfeeding self-efficacy and attitudes among 60 teen mothers, comparing those who receive the program to those who don't. The goal is to see if this extra support can improve breastfeeding outcomes in this high-risk group.

What this could mean

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

Active substance
A behavioral intervention combining theory-based antenatal education, supportive text messages, a postpartum home visit, and telephone counseling to enhance breastfeeding self-efficacy and attitudes.
What this could lead to
If effective, this program could help adolescent mothers breastfeed longer and more confidently, improving health outcomes for both mothers and babies.
What could go wrong
The trial is small (60 participants) and early-stage, so results may not apply broadly. Success depends on participant engagement and follow-up, which can be challenging in this population.

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

60 people

The number who actually took part.

Started

Mar 2025

Finished

Oct 2025

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

16 to 19 years

Sex

Female participants only

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

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: * Adolescent pregnant women aged 16-19 years * Gestational age of 32 weeks or more at enrollment * A healthy pregnancy without a known maternal or fetal complication that would interfere with participation in the study * No known maternal or fetal condition contraindicating breastfeeding * Able to communicate with the researcher and complete the study procedures * Access to a reachable telephone * Provision of written informed consent * Singleton pregnancy * Planning to breastfeed postpartum * No previous breast surgery * No psychiatric disorder * No planned relocation Exclusion Criteria: * A maternal or fetal complication identified before enrollment that could lead to pregnancy loss or prevent participation in the study * A known maternal condition contraindicating breastfeeding * A communication barrier that would prevent completion of the education, counseling, or study assessments

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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.

Adolescent pregnancy Breastfeeding Self efficacy

Contacts and locations

Locations

  • Family Health Centers Affiliated With the Eyyübiye District Health Directorate

    Sanliurfa, Şanlıurfa, Turkey (Türkiye)

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