Text Size

Satiety Response of White and Brown Rice Compared to Glucose Control

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
University of Minnesota - Clinical and Translational Science Institute
ClinicalTrials.gov Identifier:
NCT01508975
First received: January 9, 2012
Last updated: February 13, 2013
Last verified: February 2013
History of Changes
  Purpose

The investigators hypothesize that consumption of either white or brown rice will be more satiating than glucose control.


Condition Intervention
Food Selection
 Other: White Rice, Brown Rice, Glucose

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Crossover Assignment
Masking: Open Label
Primary Purpose: Prevention
Official Title: Satiety Response of White and Brown Rice Compared to Glucose Control

Resource links provided by NLM:

Drug Information available for: Dextrose
U.S. FDA Resources

Further study details as provided by University of Minnesota - Clinical and Translational Science Institute:

Primary Outcome Measures:
  • Satiety [ Time Frame: 4 hours following breakfast ] [ Designated as safety issue: No ]
    Visual analogue scales (subjective measurements)


Enrollment: 20
Study Start Date: January 2011
Study Completion Date: December 2012
Primary Completion Date: December 2012 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: white rice
White rice
 Other: White Rice, Brown Rice, Glucose
white rice, brown rice, glucose
Experimental: Brown rice
Brown Rice
 Other: White Rice, Brown Rice, Glucose
white rice, brown rice, glucose
Experimental: Glucose
Glucose
 Other: White Rice, Brown Rice, Glucose
white rice, brown rice, glucose

Detailed Description:

This study is an acute, randomized, repeated measures design with 20 subjects. Subjects will consume 3 test breakfasts, white rice, brown rice, or glucose control, each containing 400 calories. Treatments will be one week apart. After consumption of the controlled breakfast, subjects will complete visual analogue scales (VAS) for satiety response. Additionally, they will consume a pizza lunch and record food intake for the next 24 hours. Breath gas samples will be collected to estimate fermentation of fiber in the large intestine. Also, subjective data on gastrointestinal tolerance will be collected.

  Eligibility

Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • healthy subjects

Exclusion Criteria:

  • inability to consume rice for breakfast
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01508975

Locations
United States, Minnesota
Department of Food Science and Nutrition
St. Paul, Minnesota, United States, 55108
Sponsors and Collaborators
University of Minnesota - Clinical and Translational Science Institute
Investigators
Principal Investigator: Joanne Slavin, PhD University of Minnesota - Clinical and Translational Science Institute
  More Information

No publications provided

Responsible Party: University of Minnesota - Clinical and Translational Science Institute
ClinicalTrials.gov Identifier: NCT01508975     History of Changes
Other Study ID Numbers: USARice1
Study First Received: January 9, 2012
Last Updated: February 13, 2013
Health Authority: United States: Institutional Review Board

Keywords provided by University of Minnesota - Clinical and Translational Science Institute:
satiety
obesity
food intake

ClinicalTrials.gov processed this record on May 19, 2013