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Talking it out: study tests education to ease postpartum blues

NCT ID NCT07062159

Symptom relief Sponsor: Yasemin Ozhuner 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tested a psychoeducational program based on the Watson Human Caring Model to reduce depressive symptoms and strengthen mother-infant bonding after childbirth. 88 pregnant women participated. The program covered topics like postpartum depression, baby care, and bonding. The goal was to see if this supportive education could improve mental health and the mother-child relationship.

What this could mean

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

Active substance
psychoeducational intervention program
What this could lead to
If successful, this program could offer a simple, non-drug way to help new mothers feel better and bond with their babies.
What could go wrong
This is a small, completed trial with 88 participants. Results may not apply to all mothers, and the effect may be modest.

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

88 people

The number who actually took part.

Started

Jul 2025

Finished

Jan 2026

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: * • Women in their 20-35th week of pregnancy, * Volunteers, * Over 18 years of age, * Literate, * No visual, hearing or mental disabilities, * Having a healthy baby weighing over 2500 grams, * Being in the same environment with their baby after birth, * Having a healthy fetus on ultrasound will be included in the study. Exclusion Criteria: * • Those diagnosed with depression or other mental illnesses by a physician, * Those taking medication for mental illness, * Women who have given birth prematurely, * Stillbirth, * Those who have not participated in more than one interview will not be included in the study.

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Conditions

The condition(s) this trial relates to.

postpartum depression prevention target

As listed by the trial registrant

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

Mother-infant interaction Postpartum depression Psychoeducation

Contacts and locations

Locations

  • Eskisehir Osmangazi University

    Eskişehir, Odunpazarı, 26000, Turkey (Türkiye)

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