Reorganization Strategy to Optimize the Use of Virtual Reality
NCT ID: NCT07132710
Last Updated: 2025-08-20
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ACTIVE_NOT_RECRUITING
30 participants
OBSERVATIONAL
2025-03-01
2026-03-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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OTHER
PROSPECTIVE
Study Groups
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VR mask potential users in critical care
Patients and caregivers of cardiac critical care units likely to use a VR mask for therapeutic purposes
Semi-structured interviews
Patients and caregivers will be interviewed about the barriers and facilitators to the use of VR masks in the management of pain and anxiety, in order to propose organizational changes that encourage their use.
Interventions
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Semi-structured interviews
Patients and caregivers will be interviewed about the barriers and facilitators to the use of VR masks in the management of pain and anxiety, in order to propose organizational changes that encourage their use.
Eligibility Criteria
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Inclusion Criteria
* Adult patients treated in the unit with a condition requiring at least one potentially painful and anxiety-provoking invasive procedure (e.g., Central Venous Line placement, Arterial Catheter Insertion, ...) allowing the use of the VR mask.
* Patients able to understand the instructions without language barriers, to ensure the validity of the interviews and the quality of the data collected.
Exclusion Criteria
* Patients whose condition presents a medical contraindication to the use of VR mask or who present cognitive disorders.
ALL
No
Sponsors
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Hospices Civils de Lyon
OTHER
Responsible Party
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Locations
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Hôpital Louis Pradel - Hospices Civils de Lyon
Bron, France, France
Countries
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Other Identifiers
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69HCL24_1241
Identifier Type: -
Identifier Source: org_study_id
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