- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04988854
Using Models' Facial Expressions to Enhance Healthy Eating Behaviour in Children
July 26, 2021 updated by: Aston University
This study examined the effect of adults' facial expressions (FEs) whilst eating raw broccoli on children's acceptance and intake of a typically less preferred vegetable.
Investigating others' FEs in isolation (e.g., without statements about food tastiness) will improve understanding of the role of FEs in modelling of eating and contribute to developing strategies to help children learn pleasure from nutritious foods.
Based on previous literature, it was hypothesised that children's acceptance (willingness to try, and frequency of taste exposures) and intake of raw broccoli would be higher after exposure to models eating raw broccoli with positive FEs, compared to models consuming raw broccoli with neutral FEs, or a non-food control video.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Research has shown that seeing positive facial expressions towards food are effective for increasing children's desire to eat foods rated as disliked.
However, the effect of adults' positive facial expressions whilst eating a raw vegetable on children's acceptance and consumption of nutritious foods that are less preferred (e.g., vegetables) remains to be established.
This study examined the effect of unfamiliar adult models' facial expressions eating raw broccoli on children's acceptance and consumption of raw broccoli.
Children aged 4-6-year-olds were randomised to watch a video of unfamiliar adult models eating raw broccoli with a positive or neutral facial expression, or a non-food control video.
Children's acceptance (willingness to try and frequency of taste exposures) and consumption of raw broccoli was assessed.
Data about parent and child characteristics was provided by parents.
Study Type
Interventional
Enrollment (Actual)
117
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
-
-
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Birmingham, United Kingdom, B4 7ET
- Aston 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
4 years to 6 years (Child)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Child must be aged 4-6-years old. Parent and child must be living in the UK.
Exclusion Criteria:
- Children with food allergies, food intolerances, or medical conditions that affect eating behaviour were not eligible to take part.
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: Positive Condition
Children were exposed to a video of adult models eating a single piece of raw broccoli whilst showing a positive facial expression (positive video)
|
Children are randomly allocated to one of three conditions: positive, neutral or no-food control, where they will watch either a positive, neutral, or no-food control video.
|
|
Experimental: Neutral Condition
Children were exposed to a video of adult models eating a single piece of raw broccoli whilst showing a neutral facial expression (neutral video)
|
Children are randomly allocated to one of three conditions: positive, neutral or no-food control, where they will watch either a positive, neutral, or no-food control video.
|
|
Experimental: No-Food Control Condition
Children were exposed to a video of adult models putting pens away whilst showing a neutral facial expression (no-food control video)
|
Children are randomly allocated to one of three conditions: positive, neutral or no-food control, where they will watch either a positive, neutral, or no-food control video.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Raw broccoli intake
Time Frame: 5 minutes
|
Children's intake of raw broccoli (amount of grams consumed)
|
5 minutes
|
|
Willingness to try raw broccoli
Time Frame: 5 minutes
|
Children's willingness to try raw broccoli
|
5 minutes
|
|
Frequency of taste exposures to raw broccoli
Time Frame: 5 minutes
|
Children's number of oral taste exposures to raw broccoli
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5 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Katie Edwards, BSc, Aston University
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)
October 26, 2020
Primary Completion (Actual)
February 25, 2021
Study Completion (Actual)
February 25, 2021
Study Registration Dates
First Submitted
July 26, 2021
First Submitted That Met QC Criteria
July 26, 2021
First Posted (Actual)
August 4, 2021
Study Record Updates
Last Update Posted (Actual)
August 4, 2021
Last Update Submitted That Met QC Criteria
July 26, 2021
Last Verified
July 1, 2021
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- #1688
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Yes
IPD Plan Description
Non-identifiable data will be available upon request.
IPD Sharing Time Frame
IPD will be available upon request.
IPD Sharing Access Criteria
IPD will be provided when requested by researchers.
The investigators will review requests.
IPD Sharing Supporting Information Type
- Study Protocol
- Statistical Analysis Plan (SAP)
- Informed Consent Form (ICF)
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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