Activity at 25% Above the Ventilation Threshold on Appetite and Food Intake in Boys (HIE)

September 3, 2010 updated by: University of Toronto

Effect of Activity at 25% Above the Ventilation Threshold on Appetite and Food Intake After a Glucose Drink in Normal Weight Boys

The investigators hypothesize exercise increases short term appetite and food intake, and interferes with satiety and satiations to a preload in normal weight, boys.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

The effect of exercise (EXR) on short-term food intake (FI) and subjective appetite was investigated in normal weight (NW), boys were randomized into 4 treatments. Each boy consumed either a non-caloric sweetened control (CON) or GLU drink after either exercise (EXR) or sedentary activity. Subjects exercised at 25% above their ventilation threshold (VeT).

Study Type

Interventional

Enrollment (Actual)

19

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

  • Canada
    • Ontario
      • Toronto, Ontario, Canada
        • Department of Nutritional Sciences

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

9 years to 14 years (Child)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Male

Description

Inclusion Criteria:

  • Healthy boys with no emotional, behavioral or learning problems

Exclusion Criteria:

  • Girls

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: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Sedentary activity, noncaloric beverage
Other: Dietary Supplement: water with noncalorie sweetener
Experimental: Sedentary activity, glucose beverage
Other: Dietary Supplement: water with noncalorie sweetener
Experimental: Exercise activity, noncaloric beverage
Other: Activity: With noncalorie sweetener or glucose
Experimental: Exercise activity, glucose beverage
Other: Activity: With noncalorie sweetener or glucose

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
food intake (kcal)
Time Frame: at 30-35 min after the treatment
at 30-35 min after the treatment

Secondary Outcome Measures

Outcome Measure
Time Frame
Subjective appetite
Time Frame: 0-80 min
0-80 min

Collaborators and Investigators

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

Sponsor

University of Toronto

Collaborators

Canadian Institutes of Health Research (CIHR)

Investigators

  • Principal Investigator: Harvey G. Anderson, PhD., University of Toronto

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

March 1, 2009

Primary Completion (Actual)

September 1, 2009

Study Completion (Actual)

September 1, 2009

Study Registration Dates

First Submitted

September 3, 2010

First Submitted That Met QC Criteria

September 3, 2010

First Posted (Estimate)

September 8, 2010

Study Record Updates

Last Update Posted (Estimate)

September 8, 2010

Last Update Submitted That Met QC Criteria

September 3, 2010

Last Verified

September 1, 2010

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • CIHR-Kids21595_EXR2
  • CIHR (Canadian Institutes for Health Research)

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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