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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT01725425
Other study ID # 8964B
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date October 2012
Est. completion date December 31, 2024

Study information

Verified date June 2023
Source The University of Tennessee, Knoxville
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigate whether different portion sizes will effect overall mood.


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: 1. Determine the effect of increasing portion sizes on mood. 2. Determine the effect of decreasing portion sizes on mood.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 25
Est. completion date December 31, 2024
Est. primary completion date December 31, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 35 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Other:
Control
The control is designed to determine average mood.
Increase Portion Size
The purpose is to determine whether a change in mood will occur.
Decrease Portion Size
The purpose is to determine whether a change in mood will occur.
Mixed Portions
The purpose is to determine if a change in mood will occur.

Locations

Country Name City State
United States The University of Tennessee-Knoxville Knoxville Tennessee

Sponsors (1)

Lead Sponsor Collaborator
The University of Tennessee, Knoxville

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other Relative Reinforcing Value of Foods 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
Primary Total grams of snack food consumed 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. 1 year
Secondary Total grams of fruit consumed 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
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