Talking through birth fears: study tests psychoeducation for Moms-to-Be

NCT ID NCT07189767

What the study statuses mean

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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 Results may not be published yet.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
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Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 25, 2026 · Last updated Aug 25, 2026 · Updated 4 times

Summary

This study tested a nurse-led psychoeducation program for 80 first-time pregnant women who had a high perception of birth as traumatic. The program aimed to reduce that perception, improve mother-infant bonding, support breastfeeding, and lower postpartum depression. Participants were between 22 and 32 weeks pregnant and had no psychiatric illness.

What this could mean

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

Active substance
psychoeducation program
What this could lead to
If it works, this could offer a simple, non-drug way to help pregnant women feel less traumatized by childbirth and improve bonding with their baby.
What could go wrong
This is a small, completed study with 80 participants, so results may not apply to all women. The intervention is behavioral and effects may vary.

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

100 people

The number who actually took part.

Started

Apr 2023

Finished

Oct 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

18 to 35 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: * Primigravida * Between 22 and 32 weeks gestation * Experiencing a healthy pregnancy * Spontaneously pregnant * No psychiatric illness * Scored 79 or higher on the Traumatic Birth Perception Scale were included in the study. Exclusion Criteria: * High-risk pregnant women * Without a smartphone, tablet, computer or internet access

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Conditions

The condition(s) this trial relates to.

Birth Injuries

As listed by the trial registrant

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

Contacts and locations

Locations

  • Umraniye Education and Research Hospital

    Istanbul, Umraniye, Turkey (Türkiye)