Measurement of Greenhouse Gas Emissions From Meals of a University Food Operator (Cafeteria)

December 21, 2021 updated by: Véronique Provencher, Laval University
Université Laval wishes to raise awareness among students and employees in the university community so that they become aware of the impacts of their consumption choices by equipping them to adopt consumption behaviours that are favourable to the environment and their health. To do this, it is necessary to assess consumers' perception of the information available when choosing a meal to determine, among other things, whether knowledge of greenhouse gas (GHG) emissions influences their selections. In addition to this evaluation criterion, consumer perception of the nutritional quality of food will also be assessed. The nutritional composition of the meals of the characterized week will make it possible to calculate, using a nutritional profiling tool, the nutritional quality score of each meal of the day.

Study Overview

Status

Completed

Conditions

Detailed Description

This study consists of an individual meeting with each participant. This meeting will last approximately 1 hour during which each subject will choose a meal and complete various questionnaires. Subjects (male or female) will be randomly assigned to one of the four experimental conditions ("GHG", "nutrition", "GHG+nutrition" and "no logo"). Since subjects could change their eating behaviours if they knew the true purpose of the study, they will be deliberately misled when they enter the study. Participants will be recruited to participate in a market research study in which they will be invited to taste and evaluate a new meal for the cafeteria. At the end of the session, each participant will be informed of the actual objective of the study.

In this context, the general objectives of this second phase of the project are therefore:

  1. Evaluate consumer perceptions of the available information on the GHG score (in equivalent C02), the nutritional quality score and the eco-efficiency score (combination of GHG + nutrition), and;
  2. Determine if the presence of information (logo on the different scores) influences food choice and consumption among Université Laval students and staff.

Study Type

Interventional

Enrollment (Actual)

160

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

    • Quebec
      • Québec city, Quebec, Canada, G1V 0A6
        • Institute of Nutraceuticals and Functionnal Foods (INAF)

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

18 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Study or work at Université Laval

Exclusion Criteria:

  • People taking drugs that may affect appetite (e.g., antidepressants, antipsychotics or corticosteroids);
  • People with food allergies or intolerances, and pregnant and lactating women;
  • People with food aversions to more than 20% of the main meal ingredients from the menu.

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: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: GHG
Information given regarding greenhouse gas emissions via a GHG score
Participants will have to select a meal from a menu.
Experimental: Nutrition
Information given regarding nutrition via a nutrient profiling score
Participants will have to select a meal from a menu.
Experimental: GHG+nutrition
Information given regarding GHG and nutrition via a combined score
Participants will have to select a meal from a menu.
Placebo Comparator: No logo
No information given
Participants will have to select a meal from a menu.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Consumer perceptions of the meal given the information available on the GHG score, the nutritional quality score and the eco-efficiency score (combination of GHG + nutrition) vs no logo.
Time Frame: Within the year after the beginning of the study
Visual analogue scale (150mm) evaluating the perception of the participants according to the information given. Participants draw a line on the scale (between 0 and 150 mm). The higher the score, the higher the appreciation.
Within the year after the beginning of the study

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Food choice by the students and staff at Université Laval depending on the presence of information (logo on the different scores).
Time Frame: Within the year after the beginning of the study
Which meal between the 2 meals presented will be chosen by the participants given the information (logos or no logo) they received.
Within the year after the beginning of the study
Amount of the meal consumed by the students and staff at Université Laval depending on the presence of information (logo on the different scores).
Time Frame: Within the year after the beginning of the study
Measured in grams of food before and after the meal.
Within the year after the beginning of the study

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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 (Actual)

March 1, 2020

Primary Completion (Actual)

November 13, 2020

Study Completion (Actual)

April 30, 2021

Study Registration Dates

First Submitted

October 28, 2019

First Submitted That Met QC Criteria

November 4, 2019

First Posted (Actual)

November 5, 2019

Study Record Updates

Last Update Posted (Actual)

December 22, 2021

Last Update Submitted That Met QC Criteria

December 21, 2021

Last Verified

December 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • to be determined

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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