Status:

NOT_YET_RECRUITING

Preparing Kids for MRI Using VR

Lead Sponsor:

Haseki Training and Research Hospital

Conditions:

Anxiety

Sedation

Eligibility:

All Genders

5-10 years

Phase:

NA

Brief Summary

Children frequently exhibit pre-MRI anxiety that can cause motion, repeated sequences, prolonged room time, and exposure to sedation. Orientation with Virtual Reality (VR) may reduce anxiety by famili...

Detailed Description

Rationale. Pre-procedural anxiety in pediatric MRI is a well-recognized driver of motion, repetition of sequences, longer scanner occupancy, and sedation exposure. Brief, developmentally tailored expo...

Eligibility Criteria

Inclusion

  • Children 5 to 10 years old (inclusive).
  • First-ever MRI for a clinically indicated, non-emergent examination (outpatient or elective inpatient).
  • Ability to view the age-appropriate 360° VR module (head-mounted viewer or flat 360° on screen) with basic comprehension of instructions (child and/or caregiver in Turkish).
  • Parental/guardian informed consent and child assent per age/competence.
  • Standard MRI safety screening passed; institutional rescue sedation policies remain available if clinically required.

Exclusion

  • MRI contraindications (e.g., non-MR-conditional implants, unsafe metallic foreign bodies).
  • Pre-planned sedation or general anesthesia irrespective of behavior (clinician decision made prior to randomization).
  • Conditions contraindicating VR exposure (e.g., uncontrolled epilepsy, severe motion sickness/vertigo causing intolerance).
  • Severe uncorrected visual or hearing impairment precluding module viewing or instruction adherence.
  • Emergent/urgent MRI where study procedures could delay care.
  • Neurodevelopmental or behavioral conditions that render still positioning entirely unfeasible despite standard coaching (investigator judgment).
  • Prior participation in this trial (no re-enrollment).

Key Trial Info

Start Date :

October 6 2025

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

March 31 2026

Estimated Enrollment :

150 Patients enrolled

Trial Details

Trial ID

NCT07203716

Start Date

October 6 2025

End Date

March 31 2026

Last Update

October 2 2025

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