Talking through birth fears: study tests psychoeducation for Moms-to-Be
NCT ID NCT07189767
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
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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
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100 people
The number who actually took part.
- Started
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Apr 2023
- Finished
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Oct 2024
- Lead sponsor
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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
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18 to 35 years
- Sex
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Female participants only
- Healthy volunteers
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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 Hide 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.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Umraniye Education and Research Hospital
Istanbul, Umraniye, Turkey (Türkiye)