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Buzzy buzz and white noise soothe baby vaccination pain, study finds

NCT ID NCT07286721

Symptom relief Sponsor: Istanbul Arel University Source: ClinicalTrials.gov ↗

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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

Summary

This study tested two simple, drug-free methods to reduce pain in babies during routine vaccinations. 108 infants aged 2-6 months were given either white noise, a vibrating Buzzy device, or standard care. Pain was measured using a standard scale. The goal was to find easy ways to make shots less painful for babies.

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

108 people

The number who actually took part.

Started

Sep 2025

Finished

May 2026

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

2 to 6 months

Sex

Anyone

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 * Infants aged 2 to 6 months * Receiving routine hexavalent vaccination * Born at term (≥37 weeks gestation) * Medically stable at the time of vaccination * Parent or legal guardian able to provide written informed consent Exclusion Criteria * Infants with neurological disorders or developmental delay * Use of analgesic, antipyretic, or sedative medications within 24 hours prior to vaccination * Skin conditions or contraindications at the injection site * Hearing impairment that may affect response to white noise * History of adverse reactions to vaccination * Preterm infants (\<37 weeks gestation)

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As listed by the trial registrant

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

Infant pain management

Contacts and locations

Locations

  • Büyükçekmece Central Family Health Center

    Istanbul, Istanbul, 34500, Turkey (Türkiye)