VR goggles could ease pain of chest tube insertion
NCT ID NCT06247800
First seen Jun 27, 2026 · Last updated Sep 16, 2026 · Updated 4 times
Summary
This study tests whether using virtual reality (VR) during a chest drain insertion can make the experience less painful and more tolerable. About 80 adults who need the procedure will be randomly assigned to receive VR distraction or standard care. Researchers will measure satisfaction, pain, and breathlessness to see if VR helps.
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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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72 people
The number who actually took part.
- Started
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Feb 2024
- Finished
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Sep 2026
- 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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Children (under 18), adults (18 to 64) and older adults (65 and over)
- 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.
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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: * All participants undergoing ICC insertion * Participants who could understand and give consent Exclusion Criteria * Participants who are unable to understand or give consent * Ventilated patients * Participants who are not comfortable wearing VR device * Participants who are unable to communicate (illiterate, had hearing impairment, mute, blind or had memory impairment) * Participants with craniofacial deformity * Participants who are on sedative medication Traumatic or post Motor Vehicular Accident patient Participants undergoing Indwelling pleural catheter insertion Participants with anxiety disorder Exclusion Criteria: \-
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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
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National University of Malaysia
Kuala Lumpur, Kuala Lumpur, 56000, Malaysia
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Other studies related to the condition(s) this trial covers.
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