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Can a 3-Day class calm First-Time Moms' birth fears?

NCT ID NCT07268027

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tested a 3-day prenatal education program for first-time mothers to see if it could reduce fear of childbirth, change pain beliefs, and boost confidence for a normal delivery. 126 pregnant women participated, with half receiving the program and half not. The program used a constructivist approach, meaning women actively built their own understanding through group classes.

What this could mean

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

Active substance
Constructivist-Based Prenatal Education Program
What this could lead to
If successful, this program could help reduce fear and increase confidence for normal delivery in first-time mothers.
What could go wrong
This is a small, completed trial with 126 participants, so results may not apply to all pregnant women. The program is educational and has no known risks.

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

126 people

The number who actually took part.

Started

Dec 2025

Finished

Mar 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 to 45 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: * Registered in the hospital's prenatal school and actively participating in the 3-day training sessions, * Aged 18 years or older, * Between 20 and 32 weeks of gestation, * Having a singleton and low-risk pregnancy, * Primiparous (expecting their first birth), * Voluntarily agreeing to participate by signing the written informed consent form, * Able to read, understand, and communicate in Turkish. Exclusion Criteria: * Those who have previously given birth vaginally or by cesarean section (multiparous women), * Those with multiple pregnancies, * Those who conceived through assisted reproductive techniques, * Those diagnosed with serious obstetric or medical complications during pregnancy (such as preeclampsia, gestational diabetes, or risk of preterm birth), * Those with a history of psychiatric diagnosis or currently receiving psychiatric treatment, * Foreign nationals.

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Conditions

The condition(s) this trial relates to.

Pain

As listed by the trial registrant

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

Contacts and locations

Locations

  • Seyhan Çankaya

    Konya, 42250, Turkey (Türkiye)

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