Mindfulness program aims to ease childbirth fears in First-Time moms
NCT ID NCT07624253
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This study tests a 4-week online mindfulness-based psychoeducation program for first-time pregnant women who have moderate to severe fear of childbirth. The program includes relaxation exercises, emotional awareness, and coping strategies. Researchers will measure changes in fear levels, self-perception, and spiritual well-being compared to women receiving standard care.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- mindfulness-based psychoeducation program
- What this could lead to
- If it works, this could offer a simple, non-drug way to help pregnant women feel less afraid and more confident about childbirth.
- What could go wrong
- This is a small, early-stage trial with only 72 participants, so results may not apply to everyone. The intervention is online and group-based, which may not suit all women.
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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About 72 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jul 2026
An estimate. Start dates often move.
- Expected to finish
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Jul 2028
An estimate. End dates often move.
- 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 40 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: * Willing to participate in the study, * Aged between 18-40 years, * Primigravida (first pregnancy), * Not having received any childbirth preparation class, * Scoring 38 or above on the Wijma Delivery Expectancy/Experience Questionnaire, * Between 20 and 34 weeks of gestation, * Having a healthy pregnancy, * Having a singleton pregnancy, * Carrying a live fetus, * Not in active labor, * Able to speak Turkish and without any language, comprehension, or communication problems to understand and answer the questions. Exclusion Criteria: * Those who do not agree to participate in the study, * Pregnant women under 18 years of age and over 41 years of age, * Diagnosed with high-risk pregnancy, * Illiterate, * Having a contagious disease, * Having a current or past psychiatric disorder requiring treatment, * Having mobility, hearing, or psychological disabilities, * With a gestational age below 20 weeks or above 32 weeks, * Those who have entered active labor. Withdrawal / Exclusion Criteria * Participants who withdraw consent and wish to leave the study during the study period, * Participants who are unable to adapt to the intervention process, * Participants experiencing communication or internet connectivity problems, * Participants who develop complications during the intervention (e.g., onset of labor, decreased fetal movements, etc.) requiring hospitalization will be excluded from the study.
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Genom att skicka in godkänner du våra Användarvillkor
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Niğde Ömer Halisdemir Eğitim ve Araştırma Hastanesi
Niğde, Turkey (Türkiye)
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