Combined Effects of Energy Density and Eating Rate on Appetite
October 15, 2017 updated by: James Philip Karl, United States Army Research Institute of Environmental Medicine
Combined Effects of Energy Density and Eating Rate on Energy Intake and Biomarkers of Satiety
This study will examine the independent and combined effects of energy density and eating rate on appetite and endocrine mediators of appetite.
Increasing eating rate and energy intake are expected to additively increase energy intake.
Study Overview
Study Type
Interventional
Enrollment (Actual)
20
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
-
-
Massachusetts
-
Natick, Massachusetts, United States, 01760
- USARIEM
-
-
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 55 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- BMI 18-27 kg/m2
- Weight stable
Exclusion criteria:
- Chronic used of OTC or prescription drugs known to affect metabolism
- Chronic disease
- Gastric bypass surgery
- Disordered eating
- Pregnant or breastfeeding
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: Other
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Energy density
Low or high energy density meal
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Energy intake
Time Frame: 1 meal
|
1 meal
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Subjective appetite
Time Frame: 0-180 min
|
0-180 min
|
|
Postprandial peptide-YY response
Time Frame: 0-180 min
|
0-180 min
|
|
Postprandial ghrelin response
Time Frame: 0-180 min
|
0-180 min
|
|
Postprandial glucagon-like peptide-1 response
Time Frame: 0-180 min
|
0-180 min
|
|
Postprandial pancreatic polypeptide response
Time Frame: 0-180 min
|
0-180 min
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Scott J Montain, PhD, US Army Research Institute of Environmental Medicine
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
December 1, 2009
Primary Completion (Actual)
June 1, 2010
Study Completion (Actual)
June 1, 2010
Study Registration Dates
First Submitted
July 5, 2011
First Submitted That Met QC Criteria
July 29, 2011
First Posted (Estimate)
August 1, 2011
Study Record Updates
Last Update Posted (Actual)
October 17, 2017
Last Update Submitted That Met QC Criteria
October 15, 2017
Last Verified
October 1, 2017
More Information
Terms related to this study
Other Study ID Numbers
- H09-28
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.