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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NOT_YET_RECRUITING
NA
100 participants
INTERVENTIONAL
2026-03-31
2028-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Virtual reality
Intervention with virtual reality
virtual reality
Virtual reality program to reduce pain in orthopedic fractures
Standard of care
No virtual reality intervention
No interventions assigned to this group
Interventions
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virtual reality
Virtual reality program to reduce pain in orthopedic fractures
Eligibility Criteria
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Inclusion Criteria
2. Able to participate fully in all aspects of the study
3. Able to understand and sign informed consent
4. Individuals with unaided vision or those who can correct their vision using contact lenses
Exclusion Criteria
6. Self-reported history of acute and/or chronic severe motion sickness
7. The presence of a facial/head deformity that will prohibit the wearing of a VR head mounted display.
8. Legally blind or deaf
9. Have had a seizure within the past 1 year
10. Have current (within the past 30 days) clinically significant acute or chronic progressive or unstable/uncontrolled neurologic disorder
11. Have a known history of any condition or factor judged by the investigator to preclude participation in the study or which might hinder adherence
18 Years
ALL
No
Sponsors
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Mayo Clinic
OTHER
Responsible Party
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Scott A. Helgeson
Consultant, Assistant Professor of Medicine
Principal Investigators
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Scott Helgeson, MD
Role: PRINCIPAL_INVESTIGATOR
Mayo Clinic
Central Contacts
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Other Identifiers
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24-009261
Identifier Type: -
Identifier Source: org_study_id
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