Home ultrasound pushing practice: a new way to ease childbirth?
NCT ID NCT06049784
First seen Aug 18, 2026 · Last updated Aug 19, 2026 · Updated 1 time
Summary
This trial tests whether pregnant women can learn to push more effectively by using a handheld ultrasound device at home to see how their efforts move the baby's head. Participants are first-time mothers with low-risk pregnancies who plan a vaginal delivery. Some will practice with the device at home and in the hospital, some only in the hospital, and some will receive standard care. The study aims to see if this visual feedback reduces fear of childbirth, shortens the pushing stage, and improves outcomes for mother and baby.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Visual biofeedback using a self-operated home ultrasound device
- What this could lead to
- If effective, this approach could empower women to practice pushing before labor, potentially reducing fear, shortening labor, and lowering the risk of birth complications.
- What could go wrong
- The trial is relatively small and early, and results may not apply to all pregnancies. Self-operated ultrasound requires training and may not be feasible for everyone.
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 159 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Dec 2023
- Expected to finish
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Dec 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 years and older
- Sex
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Female participants only
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: * Nuliparity * Singleton pregnancy * Planned for vaginal delivery * Low risk pregnancy * Ability to fulfill a questionnaire Exclusion Criteria: * Multifetal gestation * Contraindications for vaginal delivery (Placenta previa, Breech presentation etc.) * High risk pregnancy
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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.
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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Rabin Medical Center
RECRUITINGPetah Tikva, Israel
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