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Clinical Trials/NCT04534088
NCT04534088
Completed
Not Applicable

A Virtual-reality Based Approach to Improve Behavioral Weight Management Outcomes

California Polytechnic State University-San Luis Obispo1 site in 1 country15 target enrollmentMarch 1, 2019
ConditionsWeight Loss

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Weight Loss
Sponsor
California Polytechnic State University-San Luis Obispo
Enrollment
15
Locations
1
Primary Endpoint
Intervention Satisfaction
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

A pilot randomized trial was done to test the feasibility integrating virtual reality (VR) into standard behavioral weight loss treatment.

Detailed Description

Participants with overweight or obesity are randomly assigned to a 4-week Standard Behavioral Weight Loss plus Non-Weight-Related VR app (i.e., Control Group) or Standard Behavioral Weight Loss plus Weight-Related VR app (i.e., Intervention Group). The Intervention's VR tool was designed to enable practice of behavioral skills taught in weekly group meetings, including managing social and home environmental cues for eating and activity.

Registry
clinicaltrials.gov
Start Date
March 1, 2019
End Date
November 1, 2019
Last Updated
5 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
California Polytechnic State University-San Luis Obispo
Responsible Party
Principal Investigator
Principal Investigator

Suzanne Phelan

Professor

California Polytechnic State University-San Luis Obispo

Eligibility Criteria

Inclusion Criteria

  • Non-pregnant Adults (age \> 18 years) Overweight or obesity (BMI ≥ 25) Able to speak and read in English. Available on Thursday evenings Have an iPhone 6 or higher

Exclusion Criteria

  • Self-reported serious psychological problems or medical problems

Outcomes

Primary Outcomes

Intervention Satisfaction

Time Frame: 4 weeks

Participant satisfaction ratings of virtual reality scenarios on a scale where 1 = very dissatisfied to 4 = very satisfied

Secondary Outcomes

  • Proportion of participants retained(4 weeks)

Study Sites (1)

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