Enhanced Broccoli Consumption After a Liking Norm and Vegetable Variety Message: Effects After a 24 Hour Delay.
![]() |
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
ClinicalTrials.gov Identifier: NCT02618174 |
Recruitment Status :
Completed
First Posted : December 1, 2015
Last Update Posted : December 1, 2015
|
- Study Details
- Tabular View
- No Results Posted
- Disclaimer
- How to Read a Study Record
Condition or disease | Intervention/treatment | Phase |
---|---|---|
Eating Behaviour | Behavioral: Neutral Control Condition Behavioral: Food-based Control Condition Behavioral: Health Condition Behavioral: Descriptive Social Norm Behavioral: Liking Social Norm | Not Applicable |
Using a 2 x 5 x 2 experimental design we investigated the effects of exposure to various messages on later food intake and whether any effects were sustained 24 hours after exposure in both low and high consumers of vegetables. There were three factors of delay (immediate food selection versus food selection 24 hours after exposure), message type (liking norm, descriptive norm, health message, food-based control, and neutral control message) and habitual consumption (low versus high). The buffet consisted of three raw vegetables, three energy-dense foods and two dips.
In this study the investigators hypothesised that a liking norm would increase the consumption of vegetables (compared to a neutral control condition) and that the effect would persist on vegetable consumption 24 hours after intital exposure to the liking norm.
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 400 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | Single (Participant) |
Official Title: | Enhanced Broccoli Consumption After a Liking Norm and Vegetable Variety Message: Effects After a 24 Hour Delay. |
Study Start Date : | October 2013 |
Actual Primary Completion Date : | July 2014 |
Actual Study Completion Date : | July 2014 |
Arm | Intervention/treatment |
---|---|
Placebo Comparator: Neutral Control Condition
Message about age of University of Birmingham
|
Behavioral: Neutral Control Condition
Message about age of University of Birmingham |
Placebo Comparator: Food-based Control Condition
Message about variety of vegetables in the world
|
Behavioral: Food-based Control Condition
Message about variety of vegetables in the world |
Active Comparator: Health Condition
Message about the health benefits of eating vegetables
|
Behavioral: Health Condition
Message about the health benefits of eating vegetables |
Active Comparator: Descriptive Social Norm
Message suggesting most people eat plenty of vegetables
|
Behavioral: Descriptive Social Norm
Message suggesting most people eat plenty of vegetables |
Experimental: Liking Social Norm
Message suggesting most people like eating vegetables
|
Behavioral: Liking Social Norm
Message suggesting most people like eating vegetables |
- Grams of vegetables consumed [ Time Frame: 8 months ]

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
Ages Eligible for Study: | 18 Years to 65 Years (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- Healthy volunteers
- Sufficiently fluent in English
Exclusion Criteria:
- Smokers
- Diabetes
- Food allergies
- Past / present depression or anxiety
- Past / present eating disorder.

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02618174
United Kingdom | |
University of Birmingham | |
Birmingham, West Midlands, United Kingdom, B15 2TT |
Principal Investigator: | Jason M Thomas, PhD | University of Birmingham |
Responsible Party: | University of Birmingham |
ClinicalTrials.gov Identifier: | NCT02618174 |
Other Study ID Numbers: |
UBirmingham-SNS1 |
First Posted: | December 1, 2015 Key Record Dates |
Last Update Posted: | December 1, 2015 |
Last Verified: | November 2015 |