Combined Effects of Energy Density and Eating Rate on Appetite

This study has been completed.
Sponsor:
Information provided by:
United States Army Research Institute of Environmental Medicine
ClinicalTrials.gov Identifier:
NCT01406886
First received: July 5, 2011
Last updated: July 29, 2011
Last verified: July 2011
  Purpose

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.


Condition Intervention
Appetite
Behavioral: Eating rate

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: Single Blind (Subject)
Official Title: Combined Effects of Energy Density and Eating Rate on Energy Intake and Biomarkers of Satiety

Further study details as provided by United States Army Research Institute of Environmental Medicine:

Primary Outcome Measures:
  • Energy intake [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Subjective appetite [ Designated as safety issue: No ]
  • Postprandial peptide-YY response [ Designated as safety issue: No ]
  • Postprandial ghrelin response [ Designated as safety issue: No ]
  • Postprandial glucagon-like peptide-1 response [ Designated as safety issue: No ]
  • Postprandial pancreatic polypeptide response [ Designated as safety issue: No ]

Enrollment: 20
Arms Assigned Interventions
Experimental: Energy density Behavioral: Eating rate

  Eligibility

Ages Eligible for Study:   18 Years to 55 Years
Genders Eligible for Study:   Both
Criteria

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
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01406886

Locations
United States, Massachusetts
USARIEM
Natick, Massachusetts, United States, 01760
Sponsors and Collaborators
United States Army Research Institute of Environmental Medicine
Investigators
Principal Investigator: Scott J Montain, PhD US Army Research Institute of Environmental Medicine
  More Information

No publications provided

Responsible Party: Scott Montain, PhD, USARIEM
ClinicalTrials.gov Identifier: NCT01406886     History of Changes
Other Study ID Numbers: H09-28
Study First Received: July 5, 2011
Last Updated: July 29, 2011
Health Authority: United States: Institutional Review Board
United States: Federal Government

Keywords provided by United States Army Research Institute of Environmental Medicine:
Modifiable environmental
behavioral factors

ClinicalTrials.gov processed this record on October 29, 2014