Assessing Consumer's Characterization of the Term Natural in a Food Context
NTR
1 other identifier
interventional
105
1 country
1
Brief Summary
The purpose of this project is to gain a better understanding of the underlying consumer motivations associated with choosing foods labeled as "natural"; and further, how the use of this term impacts the amount of food consumed.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable healthy
Started May 2017
Typical duration for not_applicable healthy
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
May 19, 2017
CompletedStudy Start
First participant enrolled
May 22, 2017
CompletedFirst Posted
Study publicly available on registry
May 24, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 28, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
December 28, 2018
CompletedJuly 14, 2020
July 1, 2020
1.6 years
May 19, 2017
July 13, 2020
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
One choice of 7 Label choices associated with the term 'natural'
Participant's choice of 7 Label choices associated with the term 'natural'
1 hours
Secondary Outcomes (1)
Amount of Food intake consumption according to label choices
1 hours
Study Arms (1)
Study Arm
EXPERIMENTALFood Order: Randomly assigned orders of 7 bowls of granola, each with a different food label.
Interventions
randomly assigned orders of 7 bowls of granola, each with a different food label.
Eligibility Criteria
You may qualify if:
- Aged 20-65 years' old
- Able to provide informed consent and comply with study procedures
You may not qualify if:
- Special dietary patterns that may interfere with study results
- Have allergies/intolerances to foods consumed in the study
- Have uncontrolled high blood pressure at screening visit
- Have uncontrolled elevated fasting blood glucose concentration at screening visit (≥126 mg/dL)
- History of eating disorder
- Planning to become pregnant, pregnant and/or breast-feeding
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Clinical Nutrition Research Center
Chicago, Illinois, 60616, United States
Study Officials
- PRINCIPAL INVESTIGATOR
Britt M Burton-Freeman
Illinois Institute of Technology
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 19, 2017
First Posted
May 24, 2017
Study Start
May 22, 2017
Primary Completion
December 28, 2018
Study Completion
December 28, 2018
Last Updated
July 14, 2020
Record last verified: 2020-07
Data Sharing
- IPD Sharing
- Will not share