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No-Needle gadgets take the ouch out of Kids' shots

NCT ID NCT07367659

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 several non-drug methods—like a textured plastic device called ShotBlocker, a vibrating ice pack (Buzzy), and a skin-tapping technique—to reduce pain from injections in children aged 4 to 6. 120 kids in a pediatric emergency department took part. The goal was to find a quick, effective way to make shots less painful and scary.

What this could mean

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

Active substance
ShotBlocker, Helfer Skin Tap Technique, palm stimulator, Buzzy device
What this could lead to
If effective, these simple tools could make routine injections less painful and frightening for young children in emergency settings.
What could go wrong
The trial is small (120 children) and completed, so results may not apply to all kids or settings. Pain is subjective and hard to measure accurately in preschoolers.

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

120 people

The number who actually took part.

Started

Dec 2025

Finished

Jan 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

4 to 6 years

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: * Children aged between 4 and 6 years, * An intramuscular (IM) medication order was prescribed by a physician, * The IM injection was administered in the pediatric emergency department, * No history of chronic pain-causing illness, * No diagnosis of neurodevelopmental disorders, * Had not received any analgesic medications in the past 6 hours, * No history of syncope (fainting) during previous injections, No diagnosis of mental retardation, * No scar tissue or muscle atrophy at the intended injection site, * Body mass index (BMI) percentile between the 10th and 90th percentiles for age and gender, * Both child and parent provided informed consent to participate in the study. Exclusion Criteria; * Participants were excluded from the study if: * The child was younger than 4 or older than 6 years, * There was scar tissue or muscle atrophy at the injection site, * The child or parent had communication difficulties, * The child's BMI was below the 10th percentile (cachectic) or above the 90th percentile (obese), * Either the child or parent declined to participate in the research.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

Contacts and locations

Locations

  • Sakarya University

    Sakarya, Turkey (Türkiye)

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