Glycaemic, Insulinaemic and Appetite Responses to Two Different Types of Porridge

May 1, 2012 updated by: Javier Gonzalez, Northumbria University
The purpose of this study is to assess the postprandial glycaemic, insulinaemic and appetite responses to porridge made with oats processed differently.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

13

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

  • United Kingdom
    • Tyne and Wear
      • Newcastle Upon Tyne, Tyne and Wear, United Kingdom, NE1 8ST
        • Brain, Performance and Nutrition Centre, Northumbria University

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 40 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Healthy
  • Aged 18-40 years

Exclusion Criteria:

  • Food allergies
  • Metabolic disorders

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: Prevention
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Pinhead oat porridge
Drug: Test meal
Porridge made from rolled, or pinhead oats providing 50 g of carbohydrate
Experimental: Rolled oat porridge
Drug: Test meal
Porridge made from rolled, or pinhead oats providing 50 g of carbohydrate

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Blood glucose
Time Frame: Measured at baseline, 15, 30, 45, 60, 90 and 120 min after ingestion of a test meal
Measured at baseline, 15, 30, 45, 60, 90 and 120 min after ingestion of a test meal

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Plasma insulin
Time Frame: Measured at baseline, 15, 30, 45, 60, 90 and 120 min after ingestion of a test meal
Measured at baseline, 15, 30, 45, 60, 90 and 120 min after ingestion of a test meal
Subjective appetite ratings
Time Frame: Measured at baseline, 15, 30, 45, 60, 90 and 120 min after ingestion of a test meal
Measured by a visual analogue scale (VAS)
Measured at baseline, 15, 30, 45, 60, 90 and 120 min after ingestion of a test meal

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Northumbria University

Investigators

  • Principal Investigator: Emma J Stevenson, PhD, Northumbria University

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.

General Publications

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

October 1, 2010

Primary Completion (Actual)

April 1, 2011

Study Completion (Actual)

April 1, 2011

Study Registration Dates

First Submitted

October 12, 2010

First Submitted That Met QC Criteria

October 15, 2010

First Posted (Estimate)

October 18, 2010

Study Record Updates

Last Update Posted (Estimate)

May 2, 2012

Last Update Submitted That Met QC Criteria

May 1, 2012

Last Verified

May 1, 2012

More Information

Terms related to this study

Other Study ID Numbers

  • 32W4

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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