Status:

COMPLETED

Exploring Optimal Treatment Components for Contactless Online Group-based Behavioral Weight Loss Program

Lead Sponsor:

University of South Carolina

Collaborating Sponsors:

University of Vermont

University of Tennessee

Conditions:

Obesity

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

The current pilot study will explore the optimal cost-effective treatment configuration for online group-based weight control by focusing on two aspects of our existing treatment program which have si...

Detailed Description

All participants will receive the same online group-based weight loss program, a lifestyle intervention which we have demonstrated to be effective in the past. The 16-session, goal-driven behavioral w...

Eligibility Criteria

Inclusion

  • BMI between 27-55 kg/m2
  • free of medical problems that might contraindicate participation in a behavioral weight reduction program containing an exercise component
  • must have a computer at home or work with video camera and access to the internet
  • must have a smart phone
  • only one member of a household may participate
  • must successfully complete a self-monitoring diary of food and beverages consumed for 7 consecutive days
  • must successfully set up the electronic scale (provided by the study at no cost) and transmit a body weight to study staff
  • must agree to be randomized to any of the 4 groups
  • must be willing to share access to their dietary and physical activity self-monitoring information collected via the Fitbit.com app/website and their weight data collected via linking the electronic smart scale with Fitbit.com

Exclusion

  • taking insulin
  • currently on medication that might affect weight loss
  • currently pregnant or pregnant in the previous 6 months
  • currently breastfeeding
  • enrolled in another weight reduction program
  • have had a heart attack or stroke in the past 6 months
  • ever had weight loss surgery
  • have lost more than 10 pounds in the previous 6 months
  • currently taking medications for weight loss
  • required by their doctor to follow a special diet (other than a low fat diet)
  • anyone who has a schedule that would make it difficult to attend scheduled "chat" groups, should they be randomized to receive that treatment component

Key Trial Info

Start Date :

September 23 2020

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

March 8 2021

Estimated Enrollment :

73 Patients enrolled

Trial Details

Trial ID

NCT04514900

Start Date

September 23 2020

End Date

March 8 2021

Last Update

April 30 2021

Active Locations (1)

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University of South Carolina

Columbia, South Carolina, United States, 29208