Using Bite Counter for Weight Loss: A One-month Usability Trial to Test the Effectiveness of Using the Bite Counter
NCT ID: NCT02494674
Last Updated: 2019-04-18
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
12 participants
INTERVENTIONAL
2015-07-31
2015-11-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Bite Counter tracking
Study participants will be asked to track their energy intake via a wearable device called the Bite Counter. Participants will attend weekly meetings to provide feedback on the Bite Counter.
Bite Counter tracking
Participants will be asked to use the bite counter to track all meals and provide feedback on using the bite counter for dietary self-monitoring.
Interventions
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Bite Counter tracking
Participants will be asked to use the bite counter to track all meals and provide feedback on using the bite counter for dietary self-monitoring.
Eligibility Criteria
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Inclusion Criteria
* BMI between 25- 49.9 kg/m2
* live in Columbia, South Carolina area
* be able to attend all assessment visits
* have access to the Internet, a computer, and a smartphone (iPhone, Android, etc.)
* have MD consent for participation if currently on blood pressure medications, have issues with dizziness, or have bone or joint issues
* be free of an eating disorder as screened by the Eating disorder Screen for Primary care. (If a participant has an eating disorder, they will be referred to their family physician)
* no current participation in a weight loss program or taking weight loss medications (although participants may be trying to lose weight on their own)
* able to prepare all their own meals (i.e. not living on-campus)
Exclusion Criteria
* pregnant (or have been pregnant in the last 6 months), anticipating on becoming pregnant in the next 7 months, or currently breastfeeding o Women who are pregnant should not be pursuing weight loss and should be under the direct care of a physician. Therefore women who are pregnant or who are anticipating they might be pregnant should not participate in this study. If a woman becomes pregnant during the study, she will be advised to consult her care provider and will be dropped from the weight loss study.
18 Years
65 Years
ALL
Yes
Sponsors
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University of South Carolina
OTHER
Responsible Party
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Brie Turner-McGrievy
Associate Professor
Principal Investigators
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Brie Turner-McGrievy, PhD
Role: PRINCIPAL_INVESTIGATOR
University of South Carolina
Locations
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University of South Carolina
Columbia, South Carolina, United States
Countries
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Other Identifiers
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Pro00036795
Identifier Type: -
Identifier Source: org_study_id
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