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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ACTIVE_NOT_RECRUITING
NA
20 participants
INTERVENTIONAL
2012-12-31
2025-12-31
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
OTHER
NONE
Study Groups
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EF condition
EF condition
Interventions
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EF condition
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* body mass index (BMI) between 18.5 and 24.9 kg/m2
* no history of overweight or obesity
* unrestrained eater (\<12 on Three Factor Eating Questionnaire \[TFEQ\])
* regularly participate in at least 150 minutes of moderate-intense physical activity per week over the previous 4 weeks
Exclusion Criteria
* have a medical condition affecting eating or currently following a therapeutic diet
* are currently participating in a weight loss program and/or taking weight loss medication
* have gained or lost \> 5% of body weight during the past 6 months
* diagnosed with type 1 or 2 diabetes
* have had bariatric surgery
* report disliking foods used in the investigation (scoring a 1 or 2 on a 5-point Likert scale)
* report having allergies to foods used in the investigation
* currently smoke
* report binge eating
* are graduate students in the Department of Nutrition
* are pregnant, lactating, \< 6 months post-partum.
18 Years
35 Years
ALL
Yes
Sponsors
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The University of Tennessee, Knoxville
OTHER
Responsible Party
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Hollie Raynor
Professor
Locations
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The University of Tennessee-Knoxville
Knoxville, Tennessee, United States
Countries
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Other Identifiers
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MTRI-Basic EF Study
Identifier Type: -
Identifier Source: org_study_id
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