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Fetal heartbeat sounds may soothe labor pain and fear

NCT ID NCT06271889

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 whether playing the sound of the fetal heartbeat for 3-5 minutes during active labor can lower anxiety and pain in first-time mothers. 80 pregnant women between 38-42 weeks participated. The goal is to see if this simple, non-drug approach can improve the childbirth experience.

What this could mean

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

Active substance
fetal heart sound via non-stress test device
What this could lead to
If effective, this simple, non-invasive technique could help midwives reduce anxiety and pain during labor without medication.
What could go wrong
This is a small, completed study with 80 participants. Results may not apply to all women, and the effect may be minimal or due to placebo.

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

80 people

The number who actually took part.

Started

Nov 2021

Finished

Aug 2024

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 35 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: * Who are december the age range of 18- 35, * The least literate, * Which is the primiparous, * who is at the 38-42 week of gestation * With a single pregnancy in the vertex position, * Who does not have a systemic disease that will interfere with normal delivery (gestational diabetes, preeclampsia, etc.), * Who is in the active phase of labor \* Pregnant women who have agreed to participate in the study and received informed consent will be included in the study Exclusion Criteria: * 37\. week 42. not between the weeks dec * It is a multipart, * Anyone who has any problems with communication, * Who has ceased to be involved in the study, * An unexpected complication develops (cesarean section of the pregnant woman, development of fetal distress in the fetus, etc.). * Oxytocin induction is applied Pregnant women who have been given pain medication (Aldolan, diazem) are

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Conditions

The condition(s) this trial relates to.

Labor Pain

As listed by the trial registrant

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

Contacts and locations

Locations

  • Saglık Bilimleri Universitesi

    Istanbul, Turkey (Türkiye)

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