Can partner support ease childbirth fears? new study says maybe.

NCT ID NCT06453811

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 26, 2026

Summary

This completed trial tested a two-session childbirth preparation program where spouses participated alongside first-time mothers. The program was based on self-efficacy theory and aimed to reduce fear of childbirth, improve self-confidence, and influence delivery mode. 120 couples took part, with half receiving the program plus routine care and half receiving routine care alone. The study measured fear levels, self-efficacy scores, and actual birth outcomes.

What this could mean

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

Active substance
Self-efficacy theory-based spouse participation childbirth preparation program
What this could lead to
If it works, this program could help reduce fear of childbirth and increase confidence in first-time mothers, potentially leading to more natural deliveries.
What could go wrong
This is a small, single-center study with 120 participants, so results may not apply to all populations. The program 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

120 people

The number who actually took part.

Started

Jan 2025

Finished

Jun 2025

Lead sponsor

A government agency

The lead sponsor is a government body.

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

Anyone

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: * Couples must be 18 years of age or older, * Couples should be able to read and write Turkish, * The pregnant woman has never given birth before, * The pregnant woman is at 28-30 weeks of gestation, * The pregnancy is viable and singular, * The pregnant woman does not have an established indication for caesarean section, * Routine controls during pregnancy are carried out in the hospital where the study is conducted. Exclusion Criteria: * Pregnancy achieved by assisted reproductive techniques, * Participating in a birth preparation programme other than the routine pregnancy check-ups at the hospital, * Failure to attend any of the sessions in the childbirth preparation programme, * Failure to communicate in the postnatal period (no response to at least 3 telephone calls) * Development of any indication for caesarean section during pregnancy, * The birth takes place in a health institution different from the hospital where the research will be conducted.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Childbirth preparation program are added.

Our safety recommendation!

By submitting, you agree to our Terms of use

As listed by the trial registrant

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

Contacts and locations

Locations

  • Lokman Hekim University

    Ankara, Söğütözü Mahallesi, 06510, Turkey (Türkiye)

More trials for these conditions

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