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Effect of Preoperative MRI Virtual Reality in Patients Undergoing Knee Arthroscope Surgery

Effect of Preoperative MRI Virtual Reality in Patients Undergoing Knee: a Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03426163
Enrollment
48
Registered
2018-02-08
Start date
2017-12-01
Completion date
2018-08-15
Last updated
2018-02-08

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

Conditions

Knee Injuries

Keywords

virtual reality, knee

Brief summary

Knee MRI is difficult for patients to understand as the image offers a single plane image. Accordingly,investigators sought to transfer the MRI image to 3-dimensional virtual reality system by Mesh rendering technique.

Detailed description

The primary outcome of the study is APAIS score assessed at 24 hours postoperation. Experimental VR group will be applied with virtual reality transformed knee MRI whereas no interverntion group will be applied with traditional knee MRI. MRI will be transformed to virtual reality images by Mesh rendering technique.

Interventions

DEVICEVirtual reality

Application of knee MRI transformed virtual reality system

Sponsors

Hanyang University Seoul Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Undergoing elective knee arthroscopy surgery

Exclusion criteria

* Infection, not willing to undergo study, mentally ill, severe osteoarthritis (KL grade III or more)

Design outcomes

Primary

MeasureTime frameDescription
The Amsterdam perioperative anxiety and information scale (APAIS) scorepostoperatively at 24 hourssurgery related anxiety and information score Interpretation: * minimum subscale scores: 2 * minimum combined anxiety component: 4 * maximum subscale scores: 10 * maximum combined anxiety component: 20 * The higher the scores the greater the degree of anxiety or need for additional information.

Secondary

MeasureTime frameDescription
Visual analogue scale (VAS) for satisfactionpostoperatively at 24 hoursSatisfaction scale with a range of scores from 0-100. A higher score indicates greater satisfaction.

Countries

South Korea

Contacts

Primary ContactJIN KYU M LEE, Ph.D.
jklee77@hanyang.ac.kr82-2-2290-8485

Outcome results

None listed

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