- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00837694
Snack Food Reinforcement in Obese and Non-obese Women
June 7, 2019 updated by: Jennifer Temple, State University of New York at Buffalo
Differential Effects of Daily Snack Food Intake on Reinforcing Value of Food in Obese and Non-obese Women.
Food reinforcement, motivation to obtain food, is associated with energy intake and obesity.
Finding ways to decrease the reinforcing value of unhealthy foods may help with adherence to diets and weight loss.
Our previous study in non-obese adults showed that daily consumption of the same snack food (food typically consumed outside of meals) for 14 days significantly decreased its reinforcing value.
The purpose of this study was to replicate and extend these findings to obese individuals as well as to examine effects of different portion sizes of snack foods on food reinforcement.
Thirty-one obese (body mass index > 30 kg/m2) and 27 non-obese (BMI < 30 kg/m2) women had food reinforcement and liking tested at baseline and after two weeks of daily consumption of either 0 kcal, 100 kcals, or 300 kcals daily of the same snack food.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
65
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
-
-
New York
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Buffalo, New York, United States, 14214
- University at Buffalo
-
-
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 50 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Sampling Method
Non-Probability Sample
Study Population
Women ages 18 - 50 years who were obese (body mass index >/= 30) or non-obese (BMI < 30)
Description
Inclusion Criteria:
- women
- non-smoker
- not on a diet
- no restrained eating
- had to like potential snack foods
- willing to visit the laboratory 3 times
- willing to eat snacks provided
- no medications or medical conditions that affect appetite
- no food allergies
Exclusion Criteria:
- see above
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
Cohorts and Interventions
Group / Cohort |
|---|
|
1
Non-obese/0 kcal
|
|
2
Non-obese/100 kcal
|
|
3
Non-obese/300 kcal
|
|
4
Obese/0 kcal
|
|
5
Obese/100 kcal
|
|
6
Obese/300 kcal
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of Responses Made by Clicking a Mouse Button for Food
Time Frame: During 2nd and 3rd visits
|
Participants were asked to click a button on a computer mouse and after a certaion number of responses, participants would receive a point.
After 5 points, the participants received a portion of snack food.
|
During 2nd and 3rd visits
|
|
Energy Intake
Time Frame: visits 1, 2, and 3 plus on the phone throughout the study.
|
energy contained in eaten foods and beverages
|
visits 1, 2, and 3 plus on the phone throughout the study.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Body Weight
Time Frame: visit 1 and visit 3
|
body weight
|
visit 1 and visit 3
|
|
Height
Time Frame: visits 1 and 3
|
height
|
visits 1 and 3
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Jennifer L Temple, Ph.D., University at Buffalo
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
May 1, 2007
Primary Completion (Actual)
June 1, 2008
Study Completion (Actual)
June 1, 2008
Study Registration Dates
First Submitted
February 3, 2009
First Submitted That Met QC Criteria
February 4, 2009
First Posted (Estimate)
February 5, 2009
Study Record Updates
Last Update Posted (Actual)
August 1, 2019
Last Update Submitted That Met QC Criteria
June 7, 2019
Last Verified
June 1, 2019
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Temple1
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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