The Effect of Food Labelling and Satiety on Individuals Food Choice
NCT ID: NCT03537781
Last Updated: 2018-09-19
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
NA
112 participants
INTERVENTIONAL
2018-06-12
2018-10-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
The present study aims to investigate whether the presence of nutritional information on food labels will affect participants' food choice when hungry and when satiated.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Increased Proportion of Lower Energy Density Items vs. Nutritional Labelling at an Online Supermarket
NCT04340791
Remembered Meal Satisfaction, Satiety and Later Snack Food Intake
NCT03750019
Provision of Small vs. Large Portion Sizes and Later Food Intake
NCT03241576
Increasing Availability of Lower Energy Meals vs. Menu Energy Labelling on Food Choice
NCT04336540
Attentive Eating for Weight Loss
NCT03602001
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
As there is currently little research combining these facets, it would be interesting to investigate whether individuals who are provided with food labelling information would choose unhealthy snacks when hungry as than when satiated and whether this would differ for those who are not provided with food labelling information.
Based on this, the present study aims to investigate whether the presence of nutritional information in the form of food labels will affect participants' food choice when hungry and when satiated. The General Nutrition Knowledge Questionnaire will be used to assess participants baseline nutritional knowledge and will be used as a covariate in the research project.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
OTHER
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Food label available, hungry state
foods will be displayed with food labels present and when participants had nothing to eat
Food labelling versus no food labelling
Food labelling availability and satiety status
food label available, satiated
foods will be displayed with food labels present and when participants had already eaten breaksfast
Food labelling versus no food labelling
Food labelling availability and satiety status
food label unavailable, hungry state
foods will be displayed without food labels present and when participants had nothing to eat
Food labelling versus no food labelling
Food labelling availability and satiety status
food label unavailable, satiated
foods will be displayed without food labels present and when participants had already eaten breakfast
Food labelling versus no food labelling
Food labelling availability and satiety status
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Food labelling versus no food labelling
Food labelling availability and satiety status
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria: Those who are currently following a weight loss diet; have food allergies and any medical conditions which might restrict their food intake
18 Years
65 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
St Mary's University College
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Kim Wright
Research administrator
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Conor Gissane, PhD
Role: PRINCIPAL_INVESTIGATOR
St. Mary's University, Twickenham
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
St Marys University
London, , United Kingdom
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
SMU_SHAS_2018_01.
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.