Status:

COMPLETED

A Virtual Reality Intervention to Improve Weight Maintenance

Lead Sponsor:

University of Kansas Medical Center

Conditions:

Weight Loss

Eligibility:

All Genders

21-65 years

Phase:

NA

Brief Summary

The purpose of this study is to determine if use of a virtual reality platform, Second Life, is more effective than traditional face-to-face methods for maintaining weight loss in overweight and obese...

Detailed Description

This study has two main parts. During the first 6 months (-6 to 0 months)potential subjects will be on a diet developed by researchers at the University of Kansas Medical Center (KUMC). Subsequent to ...

Eligibility Criteria

Inclusion

  • Men and women with a BMI of 25 to 39.9 kg/m2
  • Able to obtain clearance for participation from their primary care physician (PCP)
  • Have access to a computer with internet that meets Second Life system requirements

Exclusion

  • Report participating in a research project involving weight loss or PA in the previous 6 months
  • Report a regular exercise or PA program
  • Not weight stable (+/-2.27 kg) for 3 months prior to intake
  • Unwilling to be randomized to phone or 2L clinics subsequent to weight loss
  • Report being pregnant during the previous 6 months, lactating, or planned pregnancy in the following 18 months
  • Report serious medical risk such as type 1 diabetes, cancer, recent cardiac event (i.e. heart attack, angioplasty, etc.)
  • Report eating disorders as determined by the Eating Attitudes Test using a score of 20 or greater
  • Report current treatment for psychological issues, or taking psychotropic medications
  • Report adherence to specialized diet regimes, i.e., multiple food allergies, vegetarian, macrobiotic, etc.
  • Do not have access to grocery shopping and meal preparation (i.e. Military, college cafeteria plan, etc.).

Key Trial Info

Start Date :

September 1 2013

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

March 15 2020

Estimated Enrollment :

202 Patients enrolled

Trial Details

Trial ID

NCT01841372

Start Date

September 1 2013

End Date

March 15 2020

Last Update

March 25 2020

Active Locations (1)

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University of Kansas Medical Center

Kansas City, Kansas, United States, 66160