Can a Mother's mindset influence her Baby's heart tracing?
NCT ID NCT07774936
First seen Aug 19, 2026 · Last updated Aug 20, 2026 · Updated 1 time
Summary
This study looks at whether a pregnant woman's beliefs about her baby's health and her anxiety levels are linked to the results of a common fetal heart monitoring test (non-stress test) in high-risk pregnancies. Researchers will ask women at 32 weeks or later to fill out questionnaires about their health beliefs and anxiety, then compare those answers with their baby's heart rate patterns. The goal is to understand if psychological factors might play a role in how the baby's heart responds during monitoring.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If links are found, it could point toward ways to support high-risk pregnant women—like reducing anxiety—to potentially improve fetal monitoring outcomes.
- What could go wrong
- This is an observational study, so it cannot prove cause and effect. Results may be influenced by many factors and may not apply to all high-risk pregnancies.
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.
- Participants
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About 150 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Apr 2026
- Expected to finish
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Dec 2028
An estimate. End dates often move.
- Lead sponsor
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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.
Who is studied
Pregnant women at 32 weeks of gestation or later who are being followed for a high-risk pregnancy and undergo routine non-stress testing. Participants will complete the Fetal Health Locus of Control Scale and the Beck Anxiety Inventory on the same day as their routine NST.
- Ages
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18 to 45 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: * Singleton pregnancy at 32 weeks of gestation or later * Being followed for a high-risk pregnancy * No known diagnosed psychiatric disorder and no current psychiatric medication use * Absence of a fetal condition considered likely to affect the NST tracing * Maternal age between 18 and 45 years Exclusion Criteria: * Gestational age below 32 weeks and/or multiple pregnancy * Presence of a fetal condition considered likely to affect the NST tracing * Acute maternal infection or an obstetric emergency * Known diagnosed psychiatric disorder and/or current psychiatric medication use * Maternal age below 18 years or above 45 years
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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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Istanbul Training and Research Hospital
RECRUITINGIstanbul, Turkey (Türkiye)
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