- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03731273
Compensation for Smaller Portion Sizes and Portion Size Normality
November 5, 2018 updated by: Eric Robinson, University of Liverpool
Compensation for Smaller Portion Sizes and Portion Size Normality: Two Laboratory
Reducing food portion size is a potential strategy to reduce energy intake.
However it is unclear at what point consumers compensate for reductions in portion size by increasing energy intake from other items.
The investigators tested the hypothesis that reductions to food portion size will only result in significant compensatory eating when the reduced portion size is no longer visually perceived as 'normal'.
In two within-subjects experiments, participants (Study 1: N = 45, M BMI = 26.9;
Study 2: N = 37, M BMI = 26.9;
51% female) were served different sized portions of a lunchtime meal on three occasions: a 'large-normal', a 'small-normal', and a 'smaller than normal' portion.
Both the reduction from 'large-normal' to 'small-normal' and from 'small-normal' to 'smaller than normal' portions represented the same change in food volume and energy content (84g, 77kcal Study 1; 98g, 117kcal Study 2).
Participants were able to serve themselves additional helpings of the same food (Study 1), or dessert items (Study 2).
Study Overview
Study Type
Interventional
Enrollment (Actual)
90
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
-
-
Merseyside
-
Liverpool, Merseyside, United Kingdom, L69 7ZA
- Ashleigh Haynes
-
-
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
Description
Inclusion Criteria:
- general liking and willingness to consume the test foods in each study
Exclusion Criteria:
- food allergies, intolerances or specific dietary requirements (including being vegetarian or vegan)
- a history of eating disorders;
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: PREVENTION
- Interventional Model: CROSSOVER
- Masking: NONE
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Meal energy intake
Time Frame: Immediate
|
Energy intake from the served portion
|
Immediate
|
'Compensatory' (additional) energy intake
Time Frame: Immediate
|
Energy intake from additional food provided for consumption after the portion-manipulated meal
|
Immediate
|
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)
October 4, 2016
Primary Completion (ACTUAL)
July 25, 2017
Study Completion (ACTUAL)
July 25, 2017
Study Registration Dates
First Submitted
November 2, 2018
First Submitted That Met QC Criteria
November 5, 2018
First Posted (ACTUAL)
November 6, 2018
Study Record Updates
Last Update Posted (ACTUAL)
November 6, 2018
Last Update Submitted That Met QC Criteria
November 5, 2018
Last Verified
November 1, 2018
More Information
Terms related to this study
Other Study ID Numbers
- Portion size normality
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
IPD is available on the Open Science Framework https://osf.io/txf9u/
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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