- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04955002
Food Choice, Psychological Bias, and Genetic Predisposition
March 21, 2023 updated by: Catherine Graham, Oxford Brookes University
This project aims to assess if food choice is impacted by loss aversion (LA), and if this differs based on genetic predisposition to LA, in a UK healthy cohort.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Food choice, defined as how individuals decide on what to buy and eat, involves the acceptance and rejection of specific foods.
Food customisation is becoming more common amongst food retailers, allowing customers to alter their meals to their preferences by removing or adding items.
Today, food choice is viewed as more complex, food choices are not just dictated by taste but nutritional quality, allergens, and habits.
For example, the framework provided for food customisation (e.g.
pizza with toppings or a build you own pizza) and the perceived 'healthiness' of food items (e.g. the pizza toppings) can alter food choice.
Psychological reasoning, the process by which humans make decisions by drawing conclusions can play a role in food choice; however, humans can possess a psychological bias leading to illogical decision making.
Genetics can too play a role in decision making resulting in predetermined influence on food choice.
This research wishes to determine if individual's genetics can affect their food choices by researching psychological biases to food choices.
Study Type
Observational
Enrollment (Actual)
100
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Catherine Graham, PhD
- Phone Number: 3956 0186548
- Email: cgraham@brookes.ac.uk
Study Locations
-
-
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Oxford, United Kingdom
- Oxford Brookes University
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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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Male or female, adult (18+), UK-based
Description
Inclusion Criteria:
- Healthy (no known health condition)
- 18 + years of age
- UK based
Exclusion Criteria:
- Vegetarian
- Vegan
- Other dietary pattern that restricts the consumption of animal products
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Healthy UK adults
|
No intervention
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Frequency of food items remaining
Time Frame: December 2021
|
Number of food items added/removed from each decision frame
|
December 2021
|
Frequency of healthy and unhealthy items remaining
Time Frame: December 2021
|
Number of healthy and unhealthy food items added/removed from each decision frame
|
December 2021
|
Loss aversion score
Time Frame: December 2021
|
December 2021
|
|
Genotype: BDNF Val/Met (rs6265), and DRD2 ANNKK1 Taq1a/ANKK1 (rs1800497)
Time Frame: December 2021
|
December 2021
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
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)
June 9, 2021
Primary Completion (Actual)
January 1, 2023
Study Completion (Actual)
January 1, 2023
Study Registration Dates
First Submitted
June 29, 2021
First Submitted That Met QC Criteria
June 29, 2021
First Posted (Actual)
July 8, 2021
Study Record Updates
Last Update Posted (Actual)
March 22, 2023
Last Update Submitted That Met QC Criteria
March 21, 2023
Last Verified
March 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 0521_01
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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