- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01249508
Nutrition Labeling Program to Promote Healthy Dietary Patterns
December 21, 2010 updated by: University Ghent
A University Canteen-based Labeling Program to Promote Healthy Dietary Patterns
This study aims to evaluate a nutrition labelling program in improving university canteen customers' dietary pattern and behavioural determinants (e.g.
knowledge).
Study Overview
Detailed Description
The increase in diet related diseases worldwide is considered to be primarily caused by a changing environment encouraging high energy intakes and a sedentary lifestyle.
Examples of important environmental factors are the changing nature of the food supply, the changing socio-demographic structure of the population, the lack of nutrition information and the increasing reliance on foods consumed away from home.
This evolution has driven the development of measures to encourage more healthy eating patterns.
Nutrition labelling is one of those measures.
Since adults and students spend approximately half their waking hours at the workplace or university, the work or study environment is believed to be an appropriate setting to assess and try to change individuals' dietary behaviour.
This study aims to evaluate a nutrition labelling program in improving university canteen customers' dietary pattern and behavioural determinants (e.g.
knowledge).
Study Type
Interventional
Enrollment (Actual)
474
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Ghent, Belgium
- University Ghent
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
17 years to 35 years (Child, Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- university students and staff
- frequent university canteen customers
- willing to participate
Exclusion Criteria:
- non-frequent university canteen customers
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: implemented nutrition label
A one-group pre-/post-design is used for the evaluation of the university canteen-based nutrition labeling program.
This means that all participants of the program are exposed to the nutrition label implemented in the university canteen.
The subject essentially serves as its own control based on pre-test behaviour.
The nutrition label implemented is a star rating label calculated and assigned to each meal offered at the university canteens and based on the content of energy, saturated fat, sodium and fibre (expressed as vegetable portion).
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
pre-label behavioural determinants of nutrition
Time Frame: at 1 month
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Behavioural determinants of nutrition by means of quantitative questionnaire at pre-labeling implementation phase (at 1 month).
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at 1 month
|
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pre-label nutrition information processing characteristics
Time Frame: at 1 month
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Nutrition information processing by means of quantitative questionnaire at pre-labeling implementation phase (at 1 month).
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at 1 month
|
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post-label behavioural determinants of nutrition
Time Frame: at 6 months
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Behavioural determinants of nutrition by means of quantitative questionnaire at post-labeling implementation phase (at 6 months).
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at 6 months
|
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post-label nutrition information processing characteristics
Time Frame: at 6 months
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Nutrition information processing by means of quantitative questionnaire at post-labeling implementation phase (at 6 months).
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at 6 months
|
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pre-label food intake records
Time Frame: at 1 month
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Food intake by 3-day food records at pre-labeling implementation phase (at 1 month).
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at 1 month
|
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post-label food intake records
Time Frame: at 6 months
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Food intake by 3-day food records at post-labeling implementation phase (at 6 months).
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at 6 months
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
socio-demographic questionnaire
Time Frame: at 1 month
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Socio-demographical questionnaire at pre-labeling implementation phase (at 1 month).
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at 1 month
|
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pre-label physical activity registration
Time Frame: at 1 month
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Physical activity by 3-day physical activity registrations at pre-labeling implementation phase (at 1 month).
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at 1 month
|
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post-label physical activity registration
Time Frame: at 6 months
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Physical activity by 3-day physical activity registrations at post-labeling implementation phase (at 6 months).
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at 6 months
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Wim Verbeke, PhD, Prof, University Ghent
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Hoefkens C, Pieniak Z, Van Camp J, Verbeke W. Explaining the effects of a point-of-purchase nutrition-information intervention in university canteens: a structural equation modelling analysis. Int J Behav Nutr Phys Act. 2012 Sep 11;9:111. doi: 10.1186/1479-5868-9-111.
- Hoefkens C, Lachat C, Kolsteren P, Van Camp J, Verbeke W. Posting point-of-purchase nutrition information in university canteens does not influence meal choice and nutrient intake. Am J Clin Nutr. 2011 Aug;94(2):562-70. doi: 10.3945/ajcn.111.013417. Epub 2011 Jun 15.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
October 1, 2008
Primary Completion (Actual)
May 1, 2009
Study Completion (Actual)
May 1, 2009
Study Registration Dates
First Submitted
November 25, 2010
First Submitted That Met QC Criteria
November 26, 2010
First Posted (Estimate)
November 29, 2010
Study Record Updates
Last Update Posted (Estimate)
December 22, 2010
Last Update Submitted That Met QC Criteria
December 21, 2010
Last Verified
December 1, 2010
More Information
Terms related to this study
Other Study ID Numbers
- EC/2008/482
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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