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Evaluation of a Pre-surgical Virtual Reality Simulation for Cancer Surgery Patients

U

University of Manitoba

Status

Completed

Conditions

Anxiety State

Treatments

Device: Virtual reality operating room simulation

Study type

Interventional

Funder types

Other

Identifiers

NCT04544618
HS23957 (H2020:247)
322523 340300 2000 (Other Grant/Funding Number)

Details and patient eligibility

About

This study will pilot test and explore the feasibility of a virtual reality simulation of the operating room environment to reduce anxiety/distress in cancer surgery patients. Study objectives are to evaluate recruitment and data collection procedures, outcome measures, participant feedback on the virtual reality operating room intervention, and the inclusion of a treatment as usual group, and effects of the intervention on symptoms of anxiety/distress. Results of this study will inform the design of an upcoming larger-scale RCT to assess the efficacy of this intervention

Enrollment

23 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Over the age of 18
  • Can speak and read English
  • Has a cancer diagnosis
  • Scheduled/being scheduled to undergo cancer surgery under general anesthesia at the Health Sciences Centre (Winnipeg, MB)

Exclusion criteria

  • Those who do not meet any inclusion criteria
  • Those who are not competent to provide informed consent (e.g., due to cognitive impairment)
  • Those who are unable to participate in a virtual reality intervention (e.g., due to visual/auditory impairment)

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

23 participants in 2 patient groups

Intervention group
Experimental group
Description:
Participants will be exposed to a virtual reality simulation of the operating room environment for a minimum of ten minutes.
Treatment:
Device: Virtual reality operating room simulation
Treatment as usual group
No Intervention group
Description:
Participants will receive standard of care with no additional intervention aside from information received at their surgical oncology appointment and optional preoperative education classes (available to all patients).

Trial contacts and locations

1

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Central trial contact

Jordana Sommer, MA; Gabrielle S Logan, MSc

Data sourced from clinicaltrials.gov

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