Virtual nature walks may ease pain and fear during needle procedures
NCT ID NCT07696156
First seen Jul 10, 2026 · Last updated Jul 10, 2026
Summary
This study tests whether immersive virtual reality (VR) can lower stress, anxiety, and pain in adults undergoing their first central or midline catheter insertion. Participants use a VR headset showing calming nature scenes during the procedure. The goal is to see if this distraction technique improves comfort and reduces physiological stress responses.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Immersive virtual reality (IVR) with nature-themed environments
- What this could lead to
- If it works, this could provide a drug-free way to ease anxiety and pain during common hospital procedures, making care more humane.
- What could go wrong
- This is a relatively small, early-stage trial, and the effect may be modest or not generalizable to all patients. VR headsets may not be suitable 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
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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 202 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jan 2027
An estimate. Start dates often move.
- Expected to finish
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Jan 2029
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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18 years and older
- 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: * Patients ≥ 18 years old * Patients undergoing first-time CVC or Midline catheter insertion Exclusion Criteria: * Patients with cognitive impairment * Communication barriers * Acute pain (VAS \> 3) * Epilepsy * Brain neoplasm or brain metastases * Previous or simultaneous invasive procedures
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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
4 sites. 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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Fundació Althaia
Manresa, Barcelona, 08240, Spain
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Hospital Universitari de Girona Doctor Josep Trueta
Girona, Girona, 17007, Spain
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Hospital del Mar
Barcelona, Barcelona, 08003, Spain
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Hospital del Mar
Barcelona, Barcelona, 08003, Spain
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