Can personalized music ease the fear of needles in children?

NCT ID NCT07680348

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
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
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 Results may not be published yet.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
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Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jul 02, 2026 · Last updated Jul 02, 2026

Summary

This study explores whether personalized music therapy can help children aged 5 to 12 and their parents cope with repeated needle procedures, such as blood tests or injections. The therapy involves preparatory sessions where the child and parent learn music-based strategies to feel safe and regulated, followed by real-time music support during procedures. The goal is to reduce distress and improve emotional coping for both the child and the parent.

What this could mean

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

Active substance
Music therapy-based procedural support (MTPS)
What this could lead to
If effective, this approach could offer a drug-free way to reduce fear and distress for children undergoing repeated needle procedures.
What could go wrong
This is a small, early-stage study with only 20 participants, so results may not apply to all children. The intervention is behavioral and may not work 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

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 20 people

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

Expected to start

Sep 2026

An estimate. Start dates often move.

Expected to finish

Jan 2027

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

5 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: * Paediatric patient (ages 5-12) undergoing recurring needle procedures (venipuncture, intravenous (IV) cannulation, subcutaneous injections, intramuscular (IM) injections, Port-a-Cath, lumbar punctures, and bone marrow transplant, aspiration or biopsy) * Parents or caregiver of a paediatric patient (ages 5-12) undergoing recurring needle procedures. * Willing to participate in music therapy-based sessions. * Able to complete brief questionnaires and/or take part in an interview. * Paediatric inpatient, outpatient, or palliative care unit. Exclusion Criteria: * Patients currently under heavy sedation or anaesthetic medication that impairs consciousness during data collection. * Medically unstable or emergency care patients where participation may interfere with clinical care. * Non-English or non-Norwegian speakers where language barriers may pose difficulties in participants understanding study information, and issues in interpretation and analysis of collected data. * Patients with severe cognitive or developmental impairment making meaningful engagement with the intervention difficult. * Severe behavioural/psychiatric conditions that will make safe participation difficult or impossible.

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