Nature scenes vs. needles: can a sensory escape calm Kids' blood draws?
NCT ID NCT05494684
First seen Oct 13, 2026 · Last updated Oct 13, 2026
Summary
Researchers are testing whether a multisensory nature experience, using natural materials and a virtual natural setting, reduces anxiety, fear, and pain in hospitalized children aged 5 to 9 during venous blood sampling. The trial compares this approach with standard care and also measures parents' anxiety and satisfaction, plus how long the blood draw takes. About 106 children with long-term illnesses who have had blood draws before take part, and observers rate the children's anxiety from video.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a multisensory nature-based experience using natural materials and a virtual natural environment
- What this could lead to
- If it helps, hospitals could offer a low-cost, drug-free way to calm children during blood draws and other needle procedures.
- What could go wrong
- The trial is small and single-country, so results may not hold for all children or settings. Distraction approaches do not work for every child, and some may still feel fear or pain.
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 106 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Dec 2026
An estimate. Start dates often move.
- Expected to finish
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Jun 2028
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 9 years
- Sex
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Anyone
- Healthy volunteers
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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 Hide 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: 1. The child is aged between 5 and 9 years old 2. The child has a long-term illness (such as diabetes or rheumatism) 3. The child has previous experience of venous blood sampling 4. The child's level of development is age-appropriate (such as, the child is cared for at home or in day care/day nursery or attends school in the same level as the other children) 5. Child and parent understand and speak the Finnish language Exclusion Criteria: 1. The child has a diagnosis of abnormal neurological development (such as, a child has difficulty understanding spoken language or expressing emotions) 2. The child has chronic pain that has lasted more than 3 months and requires strong painkillers (opiates). 3. The child undergoes an examination or treatment during a check-up at the outpatient clinic that requires medical treatment similar to anesthesia 4. The child is taking a sedative medication.
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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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Oulu University
RECRUITINGOulu, Finland
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