- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03241576
Provision of Small vs. Large Portion Sizes and Later Food Intake
August 4, 2017 updated by: Eric Robinson, University of Liverpool
Provision of Small vs. Large Portion Sizes and Later Self-selected Food Intake: 3 Experimental Laboratory Studies in UK Participants
In 3 laboratory experiments the effect that receiving a small vs. large portion size of food has on later intake of that food was examined
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Historical increases in the size of commercially available food products have been linked to the emergence of a worldwide obesity crisis.
Although the acute effect portion size has on food intake is well established, the effect that exposure to smaller portion sizes has on future portion size selection is yet to be examined.We tested whether reducing a food portion size may 'renormalize' perceptions of what constitutes a normal amount of food to eat and result in people selecting and consuming smaller portions of that food in future.
Across three experiments participants were served a large or smaller portion of food.
In experiments 1-2, twenty four hours later participants freely selected and consumed a portion of that food.
In experiment 3, one week later participants reported on their preferred portion size of that food.
Study Type
Interventional
Enrollment (Actual)
307
Phase
- Not Applicable
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:
- 18 years or older
Exclusion Criteria:
- History of food allergy, eating disorder or currently dieting to lose weight
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: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Small portion size provision
Participants in this arm are served a small serving of a lunchtime food to eat (session 1).
|
The intervention is the small meal size participants are provided with during a lunchtime session in the laboratory.
|
Active Comparator: Large portion size provision
Participants in this arm are served a large serving of a lunchtime food to eat (session 1).
|
The intervention is the large meal size participants are provided with during a lunchtime session in the laboratory.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Later food intake (24 hour)
Time Frame: Measured 24 hours after random allocation (experiments 1 and 2)
|
Amount of the lunchtime food later chosen and consumed
|
Measured 24 hours after random allocation (experiments 1 and 2)
|
Later food intake (7 days)
Time Frame: Measured 7 days after allocation (experiment 3)
|
Amount of the lunchtime food later chosen and consumed
|
Measured 7 days after allocation (experiment 3)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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)
May 1, 2015
Primary Completion (Actual)
April 1, 2017
Study Completion (Actual)
April 1, 2017
Study Registration Dates
First Submitted
August 2, 2017
First Submitted That Met QC Criteria
August 4, 2017
First Posted (Actual)
August 7, 2017
Study Record Updates
Last Update Posted (Actual)
August 7, 2017
Last Update Submitted That Met QC Criteria
August 4, 2017
Last Verified
August 1, 2017
More Information
Terms related to this study
Other Study ID Numbers
- 463882A
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
Open science framework
IPD Sharing Time Frame
From Publication onwards
IPD Sharing Access Criteria
Openly available to all
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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