Mother's voice, recreated by AI, may calm children during surgery

NCT ID NCT07706725

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By invitation only
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Running, but no longer taking on new participants.
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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 Results may not be published yet.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.
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Cancelled before anyone took part.

Expanded access (not trials)

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Not a trial. The treatment could once be requested outside a study, but no longer can.
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When the status isn't known

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First seen Jul 16, 2026 · Last updated Jul 17, 2026 · Updated 1 time

Summary

This study tests whether listening to an AI-generated version of their mother's voice telling a story can reduce stress and confusion in children waking up from tonsil surgery. Children aged 3 to 12 will be randomly assigned to hear the AI voice, relaxing instrumental music, or standard care through headphones during the procedure. The goal is to see if the familiar voice helps them recover more calmly and with less medication.

What this could mean

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

Active substance
AI-generated maternal voice storytelling delivered through headphones
What this could lead to
If effective, this could offer a simple, non-drug way to help children recover more calmly from surgery.
What could go wrong
This is a small, early-stage trial, and the effect may be no better than relaxing music or standard care. Results may not apply to other surgeries or age groups.

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

About 90 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Jul 2026

An estimate. Start dates often move.

Expected to finish

Sep 2026

An estimate. End dates often move.

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

3 to 12 years

Sex

Anyone

Healthy volunteers

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Children aged 3 to 12 years. * Scheduled for elective adenotonsillectomy under general anesthesia. * American Society of Anesthesiologists (ASA) physical status I or II. * Written informed consent obtained from a parent or legal guardian. Exclusion Criteria: * Hearing impairment or inability to receive auditory stimulation. * Developmental delay, neurological or psychiatric disorders. * Use of sedative, antipsychotic, or anticonvulsant medications. * Known allergy or contraindication to study medications. * Refusal of participation by the parent/legal guardian.

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Conditions

The condition(s) this trial relates to.

Emergence Delirium

As listed by the trial registrant

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

How to take part

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  1. The places running it

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  2. The official record

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Contacts and locations

Locations

  • Adıyaman University

    Adıyaman, 02200, Turkey (Türkiye)

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