- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07531524
Dual-Label Intervention to Promote Low-Carbon and Healthy Food Choices in a University Cafeteria
A Dual-Label Intervention to Promote Low-Carbon and Healthy Food Choices in a University Cafeteria.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Design and Setting This study is designed as a prospective, stratified randomized controlled trial conducted in a real-world university cafeteria setting. The aim is to evaluate the isolated effect of a dual-label intervention (carbon footprint color-coding combined with calorie information) on food choice behavior without confounding from nutritional labeling. The cafeteria environment will be maintained consistently across both study arms regarding menu offerings, pricing, and food placement.
Participant Recruitment and Randomization Approximately 200 university student volunteers will be recruited. Following a 2-week baseline observation period, participants will undergo body composition analysis and will be stratified by gender, Body Mass Index and baseline dietary carbon footprint level. Within each stratum, participants will be randomly assigned in a 1:1 ratio to either the Intervention Group or the Control Group. Participants will be blinded to the specific study hypothesis (carbon reduction) during recruitment and baseline to minimize the Hawthorne effect.
Intervention and Menu Profiling Carbon Footprint Labeling: Life-cycle carbon emissions per 100g will be calculated. Dishes are categorized into three color-coded tiers using quintile distribution: Green (Low Carbon), Yellow (Medium Carbon), and Red (High Carbon).
Calorie Labeling: Explicit calorie values (kcal per 100g) will be displayed numerically.
Nutritional Quality (Hidden Variable): A Nutrient Density Score (NDS) will be calculated for each dish and classified into four grades (A, B, C, D). Crucially, this nutritional grade will NOT be displayed on labels. It serves solely as an analytical variable to assess the natural alignment between low-carbon choices and nutritional adequacy, thereby isolating the effect of carbon/calorie cues.
Study Phases
The trial spans 8 weeks in total, divided into three distinct phases:
Phase 1: Baseline Period (Weeks 1-2):
All participants select lunch from their designated windows (Intervention windows vs. Control windows). No labels are displayed during this phase. Participants will capture and upload meal photos daily via a designated system. Baseline environmental and health awareness questionnaires will be administered.
Phase 2: Intervention Period (Weeks 3-6):
Intervention Group: Food items at the designated windows will display the dual-label tags (Colored Carbon Footprint Icon + Calorie Number).
Control Group: No labels will be displayed at their designated windows. Participants continue daily photo uploads of their selected meals. To verify label exposure, the Intervention Group will be prompted to identify the color and calorie content of their selection during the check-in process.
Phase 3: Follow-up Period (Weeks 7-8):
All labels will be removed from the cafeteria. Participants continue to select meals from their originally assigned windows and upload photos. This phase assesses the sustainability of any behavioral changes induced by the label exposure.
Outcome Measures Primary Outcome: Change in the mean carbon footprint level (scored as Green=1, Yellow=2, Red=3) of selected meals from baseline to the intervention period.
Secondary Outcomes:
Implicit nutritional quality of selected meals. Changes in body composition (Body Fat Percentage, Skeletal Muscle Mass) measured pre- and post-intervention.
Changes in self-reported environmental and health awareness scores. Congruence effect: Analysis of behavioral change when carbon and calorie cues are aligned (e.g., Green + Low Calorie) versus conflicting (e.g., Green + High Calorie).
Data Collection and Analysis:
Meal selection data will be digitized daily through participant-submitted photographs. Carbon and nutritional scores will be calculated based on the backend recipe database. Statistical analysis will utilize linear mixed models to account for repeated measures within participants, comparing the differential change between the Intervention and Control groups over time.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Cun Lin
- Phone Number: +8618190275899
- Email: 202312210602027@zcmu.edu.cn
Study Locations
-
-
Zhejiang
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Hangzhou, Zhejiang, China, 310000
- Zhejiang Chinese Medicine University
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Contact:
- Cun Lin
- Phone Number: +8618190275899
- Email: 202312210602027@zcmu.edu.cn
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Students enrolled at the university
- Regularly purchase food in the university cafeteria
- Aged ≥18 years
Exclusion Criteria:
- Individuals aged <18 years
- Individuals who do not regularly purchase food in the university cafeteria
- Individuals unable to participate throughout the study period
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Food purchased with carbon and calorie labels.
Participants in this arm will select their meals from designated cafeteria windows where food items display dual labels combining carbon footprint color-coding (Green=Low, Yellow=Medium, Red=High carbon emissions per 100g) and explicit calorie values (kcal per 100g).
The intervention lasts 4 weeks, preceded by a 2-week baseline period and followed by a 2-week follow-up period without labels.
Meal selections will be recorded daily via photo uploads.
|
Participants are exposed to carbon footprint and calorie information presented on labels attached to serving trays in a university cafeteria.
The labels use visual cues (e.g., traffic-light colors) to indicate environmental impact and energy content of food items at the point of selection.
|
|
No Intervention: Control
Participants in this arm will select their meals from designated cafeteria windows where no carbon or calorie labels are displayed.
The menu offerings, pricing, and food placement remain identical to the intervention arm.
Meal selections will be recorded daily via photo uploads throughout the 2-week baseline, 4-week observation period, and 2-week follow-up phase
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Carbon footprint of selected food items
Time Frame: 4 weeks for intervention period
|
Average carbon footprint of food items selected per participant in a university cafeteria setting, calculated based on carbon emission values and compared between intervention and control groups.
|
4 weeks for intervention period
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Calorie content of selected food items
Time Frame: 4 weeks for intervention period
|
Average calorie content (kcal) of food items selected per participant in a university cafeteria setting, compared between intervention and control groups.
|
4 weeks for intervention period
|
|
Nutritional quality score of selected food items
Time Frame: 4 weeks for intervention period
|
utritional quality score of food items selected per participant in a university cafeteria setting, assessed using a predefined scoring system and compared between groups.
|
4 weeks for intervention period
|
|
Body mass index
Time Frame: Baseline and 4 weeks.
|
Change in body mass index (kg/m²) from baseline to 4 weeks among participants.
|
Baseline and 4 weeks.
|
|
Body weight
Time Frame: Baseline and 4 weeks
|
Change in body weight (kg) from baseline to 4 weeks among participants.
|
Baseline and 4 weeks
|
|
Environmental awareness score
Time Frame: Baseline to 4 weeks
|
Change in environmental awareness related to food choices, assessed via questionnaire scores and compared between groups.
|
Baseline to 4 weeks
|
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Health awareness score
Time Frame: Baseline to 4 weeks
|
Change in health awareness related to dietary choices, assessed via questionnaire scores and compared between groups.
|
Baseline to 4 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Lina Zhang, Ph.D, School of Public Health, Zhejiang Chinese Medical University
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- DLCD-2026-01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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