Food Choices in Healthy Weight Women

Sponsor
The University of Tennessee, Knoxville (Other)
Overall Status
Completed
CT.gov ID
NCT02481362
Collaborator
(none)
28
1
2
11
2.5

Study Details

Study Description

Brief Summary

This study will examine differences in habituation to foods high in sugar and fat content versus those that are not, in normal weight women.

Condition or Disease Intervention/Treatment Phase
  • Other: CAKE
  • Other: APRICOTS
N/A

Detailed Description

Participants will complete two experimental sessions, in which habituation to chocolate cake and dried apricots will be measured, with each session measuring habituation rate to one food. Upon arrival to the session, participants will write down what they have consumed and the minutes of physical activity they have engaged in during the previous 24 hours. Participants will rate their feelings of hunger and fullness using a 100mm VAS. They will also rank their liking of the food being used in the session using a 100mm VAS. Participants will be given a peanut butter flavored granola bar, containing 190 kcal, and be instructed to consume all of the bar.

Next, participants will complete a computer generated task to measure habituation to a food (chocolate cake or apricots). The computer task will be programmed at a variable interval of 120 ± 42 seconds (VI-120) reinforcement schedule, so that participants will be rewarded one point for the first response made after approximately 120s have passed. The computer task consists of two squares, one that flashes red every time a mouse button is pressed and another square that flashes green when a point is earned. The habituation phase will be 24 minutes, divided into 12, 2-minute trials, during which participants can earn points towards access to 75 kcal portions of the food that is being measured. Participants will receive the food immediately after each point is earned to consume and can continue to play the computer task while eating. Participants will be instructed that when they no longer want to earn access to the food they can go to another table and engage in the activities provided (i.e., reading magazines). After the computer task, participants will rate their feeling of hunger, fullness, and liking of the food. During the computer task the number of consecutive two-minute time blocks before responding ceases, as well as the overall pattern of responding, will be measured.

Study Design

Study Type:
Interventional
Actual Enrollment :
28 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
Single (Participant)
Primary Purpose:
Basic Science
Official Title:
Food Choices in Healthy Weight Women
Study Start Date :
Jun 1, 2015
Actual Primary Completion Date :
May 1, 2016
Actual Study Completion Date :
May 1, 2016

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Order 1

Order for sessions: Cake, apricots

Other: CAKE
For the CAKE condition, participants will play a computer task to earn points for cake that they can consume.

Other: APRICOTS
For the APRICOTS condition, participants will play a computer task to earn points for apricots that they can consume.

Active Comparator: Order 2

Order for sessions: apricots, Cake

Other: CAKE
For the CAKE condition, participants will play a computer task to earn points for cake that they can consume.

Other: APRICOTS
For the APRICOTS condition, participants will play a computer task to earn points for apricots that they can consume.

Outcome Measures

Primary Outcome Measures

  1. Grams of consumption of cake [60 minutes]

    Amount of cake consumed will be measured using the following formula: amount of cake before consumption (first weight) - amount of cake following consumption (second weight).

  2. Grams of consumption of apricots [60 minutes]

    Amount of apricots consumed will be measured using the following formula: amount of apricots before consumption (first weight) - amount of apricots following consumption (second weight).

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 35 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • body mass index (BMI) 18.5 to 24.9 kg/m2

  • nonsmokers

  • not allergic to the foods used in the investigation

  • must like the foods in the investigation (scoring > 50 mm on a visual analogue scale [VAS])

  • be willing to consume the foods

  • not have dietary restrictions

  • not be a restrained eater (scoring > 12 on the Three Factor Eating Scale)

  • not be on medications that influence appetite

  • not planning to change their diet or physical activity during the time frame of their study participation

  • not dieting or trying to lose weight.

Exclusion Criteria:
  • BMI outside of the range 18.5-24.9

  • smoker

  • food allergies

  • does not like the foods used in the study

  • has dietary restrictions

  • is a restrained eater

  • on medications that may influence appetite

  • planning on changing diet or physical activity during time frame of the study

  • dieting

  • trying to lose weight

Contacts and Locations

Locations

Site City State Country Postal Code
1 Healthy Eating and Activity Laboratory, University of Tennessee Knoxville Tennessee United States 37996

Sponsors and Collaborators

  • The University of Tennessee, Knoxville

Investigators

  • Principal Investigator: Hollie Raynor, PhD, University of Tennessee, Knoxville

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Hollie Raynor, Professor, The University of Tennessee, Knoxville
ClinicalTrials.gov Identifier:
NCT02481362
Other Study ID Numbers:
  • UTK IRB-15-02330-XP
First Posted:
Jun 25, 2015
Last Update Posted:
Apr 5, 2018
Last Verified:
Apr 1, 2018
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 5, 2018