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Not yet recruiting NCT07660952

Effect of IE Glasses on MRI Patient Outcomes

No phase Interventional MRI-related Anxiety MRI Completion Rate

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Immersive entertainment glasses, Standard of Care: Anesthesia, Standard of Care: Sedative.
Who it may be relevant to
Registry conditions: MRI-related Anxiety, MRI Completion Rate. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

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

Overview

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

Interventions

  • Device Immersive entertainment glasses
    Use of immersive entertainment glasses during the MRI procedure.
  • Drug Standard of Care: Anesthesia
    Patient receives anesthesia as ordered by the physician.
  • Drug Standard of Care: Sedative
    Patient receives a sedative as ordered by the physician.

Primary outcome measures

  • Anxiety relief (self-report measure 2 - Visual Analog Scale for Anxiety) [Time frame: 15 to 120 minutes (depends on the duration of the MRI procedure)]
  • Anxiety relief (physiological measure - heart rate) [Time frame: 15 to 120 minutes (depends on the duration of the MRI procedure)]
  • MRI completion rate [Time frame: Immediately after the MRI procedure.]
  • MRI Image Quality [Time frame: Immediately after the MRI procedure.]

Eligibility criteria

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Non-randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Supportive care

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07660952 · 2355080

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗