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Clinical Trials in China / NCT07531524
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Dual-Label Intervention to Promote Low-Carbon and Healthy Food Choices in a University Cafeteria

NCT07531524 · tracked via the Priya Life Science China tracker
Sponsor
Lina Zhang
Phase
Not applicable
Started
2026-05
Last updated
2026-04-21

Condition(s) studied

Eating BehaviorDietary Behavior

Investigational drug(s) / intervention(s)

Carbon and Calorie label

Carbon and Calorie label: 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.

Study summary

This study aims to evaluate whether a dual-label intervention, combining carbon -coded footprint color labels and calorie information, can promote low-carbon and healthier food choices among university students in a real-world cafeteria setting. A randomized controlled trial will be conducted with approximately 200 participants, who will be assigned to either an intervention group (with labels) or a control group (without labels). The study a consists of 2-week baseline period, a 4-week intervention period, and a 2-week a follow-up period. The primary outcome is the mean carbon footprint level of selected meals, and secondary outcomes include nutritional quality, body composition, and changes in environmental and health awareness.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
Accepted
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

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Zhejiang Chinese Medicine University Hangzhou Zhejiang
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07531524 on ClinicalTrials.gov ↗ ← All trials in China