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NCT04534088 Clinical Trial

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

Weight Loss Clinical Trial

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

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04534088
Other study ID # VH-CP
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 1, 2019
Est. completion date November 1, 2019

Study information
Verified date September 2020
Source California Polytechnic State University-San Luis Obispo
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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

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.

Recruitment information / eligibility
Status Completed
Enrollment 15
Est. completion date November 1, 2019
Est. primary completion date April 1, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility 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

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• Standard Behavioral Weight Loss plus Non-Weight-Related VR app
Standard Behavioral Weight Loss Program
• Standard Behavioral Weight Loss plus Weight-Related VR app
Standard Behavioral Weight Loss plus Weight-Related VR app

Locations
Country Name City State
United States Cal Poly San Luis Obispo California

Sponsors (1)
Lead Sponsor Collaborator
California Polytechnic State University-San Luis Obispo

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Other weight loss weight loss from baseline 4 weeks
Primary Intervention Satisfaction Participant satisfaction ratings of virtual reality scenarios on a scale where 1 = very dissatisfied to 4 = very satisfied 4 weeks
Secondary Proportion of participants retained Number of participants who complete the final assessment divided by the number of participants enrolled at baseline 4 weeks
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