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Clinical Trials/NCT05141214
NCT05141214
Completed
Not Applicable

Virtual Reality as a Dietary Education Adjunct for Pediatric Patients With Obesity: A Pragmatic, Randomized Pilot Study

Stanford University1 site in 1 country48 target enrollmentFebruary 24, 2023
ConditionsDiabetes

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Diabetes
Sponsor
Stanford University
Enrollment
48
Locations
1
Primary Endpoint
Immediate behavior modification
Status
Completed
Last Updated
last year

Overview

Brief Summary

Childhood obesity is a national crisis, effecting up to 1 in 5 of children in the US. In the Lucile Packard Children's Hospital Pediatric Weight Management Clinic, the investigators educate parents and caregivers about the importance of dietary modification. In addition to physician guidance, the investigators partner with registered dieticians to counsel families during an hour-long interview. However, traditional methods of education are limited by long-term recall. A typical person only recalls 2- 3% of didactic content after a period of 30 days. In order to improve recall and increase involvement of our pediatric patients in their own dietary modifications, the investigators propose a pragmatic, randomized pilot study investigating the effectiveness of Virtual Reality (VR) in changing dietary choices and improving recall.

Registry
clinicaltrials.gov
Start Date
February 24, 2023
End Date
August 15, 2023
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Thomas Caruso

Clinical Professor

Stanford University

Eligibility Criteria

Inclusion Criteria

  • Ages 6-18 years of age
  • Able to consent or have parental consent
  • Diagnosis of Obesity Grade 1, 2 and 3 at LPCH/SHC facilities

Exclusion Criteria

  • People who do not consent
  • Significant Cognitive Impairment
  • History of Severe Motion Sickness
  • Visual Problems

Outcomes

Primary Outcomes

Immediate behavior modification

Time Frame: Duration of appointment, typically 2-3 hours

Immediate behavior modification will be assessed by comparing the selection of an appointment exit reward the end of the study visit. Participants will be presented with two options, either a bag of chips or a healthier alternative. Selection of reward will be recorded.

Secondary Outcomes

  • Nutritional knowledge survey(Duration of appointment, typically 2-3 hours)
  • Pediatric Adapted Liking Survey(Duration of appointment, typically 2-3 hours)
  • Satisfaction Survey(Duration of appointment, typically 2-3 hours)

Study Sites (1)

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