Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07246746

Use of an Infotainment System in MRI in Patients Suffering From Unexpected Anxiety.

Led by Centre Hospitalier Universitaire Dijon · Updated on 2026-01-15

50

Participants Needed

1

Research Sites

102 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

MRI scans are now considered essential for diagnosing or monitoring disease, and as a result, the number of MRI scans has increased significantly in recent years. Nevertheless, these routine examinations remain a source of apprehension and anxiety for some people. The objective of this study is to compare two methods of care, enabling anxious individuals to complete their MRI examination and obtain images of sufficient quality for the radiologist to read and interpret.

CONDITIONS

Official Title

Use of an Infotainment System in MRI in Patients Suffering From Unexpected Anxiety.

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Individuals who have given their verbal consent
  • Individuals over the age of 18
  • Hospitalized or ambulatory individuals who are able-bodied and scheduled to undergo a brain MRI scan on the 1.5T A MRI machine at the Dijon University Hospital
  • Individuals reporting anxiety about brain MRI for the first time upon admission by the radiology technician
Not Eligible

You will not qualify if you...

  • Persons not affiliated with or not covered by a social security system
  • Persons subject to legal protection measures (guardianship, trusteeship)
  • Persons subject to judicial protection measures
  • Women who know they are pregnant
  • Adults who are incapable or unable to give their consent
  • Persons with contraindications to MRI
  • Persons who have already undergone an MRI accompanied by hypnosis
  • Persons who do not speak French
  • Persons who cannot read French
  • Persons with cognitive disorders
  • Persons who have taken sedatives before the examination
  • Persons who regularly take anxiolytic medication and have increased their usual dose before the examination
  • Persons who have already participated in the study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

CHU Dijon Bourgogne

Dijon, France

Actively Recruiting

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Research Team

N

Nicolas MIGNOT

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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