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Clinical Trials/NCT07660952
NCT07660952Not yet recruitingNot Applicable

Examining the Effect of Immersive Entertainment Glasses on Magnetic Resonance Imaging-related Patient Outcomes

Baptist Health South Florida0 sites300 target enrollmentStarted: July 1, 2026Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
300

Study Overview

Brief Summary

Examine the effect of immersive entertainment glasses (IEG) on patients' claustrophobia-associated anxiety levels during magnetic resonance imaging (MRI).

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Adult patients at least 18 years of age
  • Outpatients/inpatients scheduled for an MRI with anesthesia
  • Inpatients scheduled for an MRI with an IV/PO sedative

Exclusion Criteria

  • Pregnant patients

Arms & Interventions

Control Group 1

Active Comparator

Patients who receive anesthesia (general or conscious sedation) for completion of their MRI scans as ordered by the physician.

Intervention: Standard of Care: Anesthesia (Drug)

Control Group 2

Active Comparator

Patients who receive oral or intravenous sedation [i.e., benzodiazepines such as lorazepam (Ativan), diazepam (Valium), alprazolam (Xanax), or equivalent] for completion of their MRI scans, as ordered by the physician.

Intervention: Standard of Care: Sedative (Drug)

Intervention Group

Experimental

Patients scheduled for MRIs with anesthesia or a sedative choose to use the immersive entertainment glasses (instead of the physician-ordered anesthesia or sedative) for completion of their MRI scans.

Intervention: Immersive entertainment glasses (Device)

Investigators

Sponsor
Baptist Health South Florida
Sponsor Class
Other
Responsible Party
Sponsor

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