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Music eases anxiety for Moms-to-Be during fetal monitoring

NCT ID NCT07299214

Symptom relief Sponsor: Karamanoğlu Mehmetbey University Source: ClinicalTrials.gov ↗

What the study statuses mean

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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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at whether playing music during a non-stress test (a routine check on the baby's heartbeat) helps pregnant women feel more comfortable and less anxious. 173 women took part. Researchers measured their comfort, blood pressure, heart rate, and anxiety levels. The goal was to see if a simple, drug-free approach like music could improve the experience.

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

173 people

The number who actually took part.

Started

Jun 2025

Finished

Aug 2025

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 45 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: * Women aged 18-45 years * Completion of at least the 32nd week of gestation * No pregnancy-related risk factors (e.g., premature rupture of membranes, preeclampsia, gestational diabetes) * No multiple pregnancy * Normal blood pressure levels (not ≤80/60 mmHg and not ≥140/90 mmHg) * Having eaten at least two hours before the NST procedure * No smoking or alcohol consumption for at least two hours before the NST procedure * Ability to communicate effectively * No hearing impairment * Voluntary participation in the study Exclusion Criteria: * Pregnant women with fetal distress * Cases for whom the physician considered emergency intervention necessary * Individuals with an impaired NST requiring immediate intervention * Individuals with a diagnosed psychiatric disorder * Individuals with hearing impairment

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Conditions

The condition(s) this trial relates to.

anxiety disorder

As listed by the trial registrant

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

Pregnant women

Contacts and locations

Locations

  • University District, 2076 Street, No: 11

    Karaman, Central, 70200, Turkey (Türkiye)

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