Calming senses before surgery: a new way to soothe anxious kids?
NCT ID NCT07769788
First seen Aug 18, 2026 · Last updated Aug 20, 2026 · Updated 2 times
Summary
This trial tests whether a brief multisensory stimulation session before a pediatric surgery clinic visit can lower anxiety and fear in children aged 5 to 10, as well as reduce parental anxiety. Children undergoing their first surgical evaluation will be randomly assigned to receive either the stimulation or standard care. The study measures anxiety and fear levels using child-friendly scales to see if this simple, non-drug approach can make medical encounters less stressful.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Multisensory stimulation (a calming combination of sensory inputs, such as soothing sounds, lights, or textures) given before a clinical encounter.
- What this could lead to
- If effective, this simple, non-drug approach could offer a practical way to ease anxiety and fear in children before medical visits, improving cooperation and the overall experience for families.
- What could go wrong
- This is a small, early-stage trial, so results may not apply broadly. The effect may be modest, and individual responses to sensory stimulation can vary.
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
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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
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About 80 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jul 2026
An estimate. Start dates often move.
- Expected to finish
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Sep 2026
An estimate. End dates often move.
- Lead sponsor
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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
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5 to 10 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * For the children to be sampled, the inclusion criteria plan to involve children who: * Are aged between 5 and 10 years, * Are undergoing their first outpatient pediatric surgery evaluation, * Have no prior history of surgery, and Agree (along with their parents) to voluntarily participate in the study. Exclusion Criteria: * For the children to be sampled, the exclusion criteria plan to omit children who: * Are in unstable general condition or require emergency medical intervention, * Have intellectual disabilities, or Have visual or hearing impairments.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Bilecik Seyh Edebali University
Bilecik, Turkey, 11230, Turkey (Türkiye)
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