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Clinical Trials/ACTRN12622000085774
ACTRN12622000085774
Completed
未知

A single-centre, randomised controlled trial investigating the effect of 3D virtual reality technology compared to 2D video images on distress during anaesthetic induction in children

Child & Adolescent Health Service Executive at Perth Children's Hopsital0 sites200 target enrollmentJanuary 21, 2022

Overview

Phase
未知
Intervention
Not specified
Conditions
Children undergoing elective or emergency surgery
Sponsor
Child & Adolescent Health Service Executive at Perth Children's Hopsital
Enrollment
200
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
January 21, 2022
End Date
July 15, 2022
Last Updated
3 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Child & Adolescent Health Service Executive at Perth Children's Hopsital

Eligibility Criteria

Inclusion Criteria

  • Children aged 4\- 13 years of age undergoing elective or emergency surgery at Perth Children's Hospital

Exclusion Criteria

  • Any visual, auditory, or cognitive impairments preventing interaction with the VR intervention, particularly a history of epilepsy or seizures
  • Any critical medical condition or condition that precludes the use of VR
  • Methicillin resistant Staphylococcus aureus infection or symptoms of respiratory or gastrointestinal infection that may contaminate VR equipment. VR equipment and the iPad will be cleaned with standard equipment cleaning policies aligned with all theatre equipment.
  • Children receiving midazolam or ketamine as a premedication
  • VR headset does not fit patient at the researchers discretion
  • Any concern in the ability of the parents/guardian or child to appropriately adhere to the study protocol or any issues which, in the investigator’s opinion, would increase the risks of study participation to the child.
  • Language barriers impeding data collection
  • Department for child Protection and Family Support is involved in their care

Outcomes

Primary Outcomes

Not specified

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