Status:
COMPLETED
VR Usage in Non-Invasive Surgical Sub-Specialty Procedures
Lead Sponsor:
Stanford University
Conditions:
Stress, Emotional
Stress, Psychological
Eligibility:
All Genders
2-18 years
Phase:
NA
Brief Summary
Preprocedural, preoperative, and prevascular access anxiety in pediatric patients has been previously shown to increase the likelihood of family stressors, agitation, sleep disturbances, and negative ...
Detailed Description
Anxiety among children undergoing non-invasive surgical subspecialty procedures is common. Not only is high anxiety traumatic, but research in a surgical setting indicates that high anxiety in childre...
Eligibility Criteria
Inclusion
- Be between ages of 2-18 years of age
- Have comprehension of instructions in the English language
- Have parental consent
- Pediatric patients must be undergoing non-invasive surgical subspecialty procedures at an Lucile Packard Children's Hospital (LPCH) out-patient clinic
- Children who are normally healthy (ASA I) or have a mild systemic disease (ASA II,III)
Exclusion
- Significant cognitive impairment/developmental delays per parental report or H\&P.
- Children with ASA IV (severe systemic disease that is a constant threat to life) or ASA V (unstable patients not expected to survive \>24 hours or without the operation)
- Children currently taking psychotropic mediations will be excluded from this study due to the affect emotion modulation
- Strong parental or patient preference for pharmacological anxiolytic
- Strong parental or patient preference for specific anxiety-reducing technique
Key Trial Info
Start Date :
October 16 2017
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 11 2023
Estimated Enrollment :
291 Patients enrolled
Trial Details
Trial ID
NCT03464955
Start Date
October 16 2017
End Date
July 11 2023
Last Update
September 28 2023
Active Locations (1)
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1
Lucile Packard Children's Hospital at Stanford
Palo Alto, California, United States, 94304