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

Status

Recruiting

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT07246746

Acronym

USIA

Enrollment

Registered

2025-11-24

Start date

2026-01-12

Completion date

2028-01-31

Last updated

2026-01-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Unexpected Anxiety

Brief summary

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.

Interventions

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

Assessment of patient anxiety

OTHERAnxiety support procedure according to randomization: Innovision© or Hypnosis

Hypnosis or Innovision device

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

OTHER

Masking

SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

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

Design outcomes

Primary

Measure	Time frame
Percentage of brain MRI sequences reported as interpretable	Baseline

Countries

France

Contacts

Primary ContactNicolas MIGNOT

nicolas.mignot@chu-dijon.fr03 80 29 30 31

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026