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Could respectful care after birth boost breastfeeding and mental health?

NCT ID NCT07280000

Knowledge-focused Sponsor: ilayda sel 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 This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 will test whether training nurses and midwives in respectful maternity care and using a structured action plan can improve outcomes for mothers and newborns after birth. Researchers will compare women who receive standard care with those who receive care after the training. The goal is to see if this approach leads to better experiences, higher breastfeeding rates, and improved mental health for new mothers.

What this could mean

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

Active substance
Respectful Maternity Care Training and Action Plan
What this could lead to
If it works, this could point toward a simple, low-cost way to improve postpartum care quality, maternal satisfaction, and breastfeeding rates.
What could go wrong
This is an early-stage, single-site study comparing groups before and after training, so results may not apply elsewhere. The intervention is behavioral, so effects may be modest or hard to sustain.

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 500 people

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

Expected to start

Dec 2025

An estimate. Start dates often move.

Expected to finish

Dec 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 to 49 years

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: * Postpartum women aged 18 years and older * Gave birth at 37-42 gestational weeks (vaginal or cesarean) * Have a single, healthy newborn * No chronic medical conditions * No history of high-risk pregnancy or fetal complications * No communication barriers (e.g., visual or hearing impairment) * Able to speak and understand Turkish * Literate and able to read and write in Turkish Exclusion Criteria: * Development of maternal or neonatal complications during the postpartum follow-up period * Inability to reach the mother at the 8-week postpartum follow-up

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Conditions

The condition(s) this trial relates to.

Breast Feeding postpartum depression

As listed by the trial registrant

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

Breastfeeding Maternal health care Maternal satisfaction Newborn health Postpartum care Postpartum depression (PPD) Quality of care

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Bakırköy Dr. Sadi Konuk Training and Research Hospital

    Istanbul, Turkey (Türkiye)

More trials for these conditions

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