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OpenTrials
Recruiting

NCT Number: NCT07246746

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

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.

Recruiting

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Key information

Conditions

Unexpected Anxiety

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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.

Exclusion criteria

  • 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

Treatment and study plan

Assessment of patient anxiety through self-administration of the State Anxiety Inventory Form Y-A questionnaire

Other

Assessment of patient anxiety

Anxiety support procedure according to randomization: Innovision© or Hypnosis

Other

Hypnosis or Innovision device

Primary outcomes

  1. Percentage of brain MRI sequences reported as interpretable

    Time frame: Baseline

Study contacts

Contact information is provided by the study sponsor or research team.

Nicolas MIGNOT

CONTACT

[email protected]

03 80 29 30 31

Sponsors and collaborators

Lead sponsor

Centre Hospitalier Universitaire Dijon

Other

Registry information

Acronym: USIA

Important dates

Study start
2026
Primary completion
2028
Study completion
2028
First posted
Nov 24, 2025
Registry last updated
Jan 15, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.