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Assessing the Bite Counter

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

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02763358
Enrollment
42
Registered
2016-05-05
Start date
2016-03-31
Completion date
2017-03-31
Last updated
2018-07-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Weight Loss

Keywords

obesity, weight loss

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).

Interventions

This study is a 15-week assessment of the possible utility of a wrist-worn device, the Bite Counter, in assisting the weight loss behavior change efforts of overweight and obese individuals. The Bite Counter tracks and analyzes wrist motions to identify those associated with taking bites of food and drinking beverages. It also has a step-counter feature. This study is designed to determine if using the Bite Counter with specific goals to reduce the numbers of bites and increase the numbers of steps will result in those changes.

Sponsors

Clemson University
CollaboratorOTHER
Medical University of South Carolina
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frame
Reduction in the numbers of bites per day as displayed on the Bite Counter15 weeks

Secondary

MeasureTime frame
Increase in the number of steps per day as displayed on the Bite Counter15 weeks

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026