- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01725425
The Effect of Portion Sizes on Mood
June 17, 2023 updated by: Hollie Raynor, The University of Tennessee, Knoxville
The Impact of Portion Size of Foods on Mood in Normal Weight Adults 18-35
The purpose of this study is to investigate whether different portion sizes will effect overall mood.
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Detailed Description
The objective of this investigation is to determine whether participants will have a change in mood based on the portion size of foods served. The specific aims of the study are:
- Determine the effect of increasing portion sizes on mood.
- Determine the effect of decreasing portion sizes on mood.
Study Type
Interventional
Enrollment (Estimated)
25
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
-
-
Tennessee
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Knoxville, Tennessee, United States, 37996-1920
- The University of Tennessee-Knoxville
-
-
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 to 35 years (Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Age 18-35
- have a body mass index of 18.5 and 24.9 kg/m^2
- be an unrestrained eater( scoring less than 12 on the Three Factor Eating Questionnaire)
- Report Being a non-smoker
Exclusion Criteria:
- currently pregnant or nursing
- report being an athlete in training
- currently taking any medications that affect appetite or food intake
- Have a medical condition affecting eating or are currently following a therapeutic diet
- Report disliking foods used in the investigation
- Report having allergies to foods used in the investigation
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: Treatment
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Control
Participants will receive equal amounts of foods.
|
The control is designed to determine average mood.
|
Experimental: Increase Portion Size
Participants will receive increased portion sizes.
|
The purpose is to determine whether a change in mood will occur.
|
Experimental: Decrease Portion Sizes
Participants will receive decreased portion sizes.
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The purpose is to determine whether a change in mood will occur.
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Experimental: Mixed Portion Sizes
Participants will receive mixed portion sizes.
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The purpose is to determine if a change in mood will occur.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Total grams of snack food consumed
Time Frame: 1 year
|
The snack food consumed in this investigation is Lays Potato Chips (Frito-Lay Inc., Plano, TX).
Participants will be provided 50 or 100 grams of this food at all sessions depending on which condition they are randomized into.
The chips provided to participants in each condition will be measured in grams to the tenth decimal point on an electronic food scale (Denver Instrument Co., Arvada, CO) before and after the session.
The weight of the container will also be measured.
Total grams of chips consumed during the session will be determined by subtracting pre- and post-consumption weight of the chips.
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1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Total grams of fruit consumed
Time Frame: 1 year
|
The fruit used in this investigation is red grapes.
Participants will be provided 100 grams or 150 grams of red grapes depending on which of the four groups they are participating in.
Each individual will go through all four conditions in this investigation.
Fruit provided to participants in each condition will be measured in grams to the tenth decimal point on an electronic food scale (Denver Instrument Co., Arvada, CO) before and after the session.
The weight of the container will also be measured.
Total grams of fruit consumed during the session will be determined by subtracting pre- and post-consumption weight of fruit.
|
1 year
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Relative Reinforcing Value of Foods
Time Frame: 1 Year
|
As part of the investigation, participants will play a computer game which assesses the relative reinforcing value of the foods used.
The number of points earned for each of the foods will be used to assess the relative reinforcing value of the foods.
|
1 Year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Hollie Raynor, PhD, University of Tennessee
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 1, 2012
Primary Completion (Actual)
December 31, 2018
Study Completion (Estimated)
December 31, 2024
Study Registration Dates
First Submitted
November 8, 2012
First Submitted That Met QC Criteria
November 9, 2012
First Posted (Estimated)
November 12, 2012
Study Record Updates
Last Update Posted (Actual)
June 22, 2023
Last Update Submitted That Met QC Criteria
June 17, 2023
Last Verified
June 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- 8964B
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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