Skip to main content
Clinical Trials/NCT02763358
NCT02763358
Completed
Phase 1

Assessing the Bite Counter as a Tool for Food Intake Monitoring: Phase II

Medical University of South Carolina1 site in 1 country42 target enrollmentMarch 2016
ConditionsWeight Loss

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Weight Loss
Sponsor
Medical University of South Carolina
Enrollment
42
Locations
1
Primary Endpoint
Reduction in the numbers of bites per day as displayed on the Bite Counter
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

This study is designed to test the usability of the Bite Counter in an attempt to reduce participants' daily bites while also increasing their daily steps.

Detailed Description

Self-monitoring is an important component of behavioral management of obesity. The Bite Counter is a wrist-worn device which detects the motions characteristic of taking a bite of food or a drink of liquid, to provide the wearer with a cumulative count of bites and sips over the day. In earlier studies the method was shown to accurately count bites across a wide variety of foods, utensils and subject demographics, and to provide an unbiased intake measurement. The proposed work will continue to improve the bite counting method by adapting to varying eating rates, develop a self-managed bite count-based weight loss protocol, and perform an independent test of the protocol. An improved Bite Counter device will also measure activity (steps).

Registry
clinicaltrials.gov
Start Date
March 2016
End Date
March 2017
Last Updated
7 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Participants must be between the ages of 18 and 70 (inclusive)
  • Participants must have a BMI between 27 and 35
  • Participants must have regular and reliable access to a Windows-based computer with an internet connection with USB connectivity
  • Participants must be currently consuming at least 1400 calories per day
  • Participants must demonstrate adequate compliance with using Bite Counter and uploading data during the two-week baseline period

Exclusion Criteria

  • Participants must have no history of any eating disorder
  • Participants must not have participated in a weight loss program within the month prior to baseline

Outcomes

Primary Outcomes

Reduction in the numbers of bites per day as displayed on the Bite Counter

Time Frame: 15 weeks

Secondary Outcomes

  • Increase in the number of steps per day as displayed on the Bite Counter(15 weeks)

Study Sites (1)

Loading locations...

Similar Trials