- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03722251
Active Video-game Playing and Food Intake in Children
October 25, 2018 updated by: Nick Bellissimo, Ryerson University
Active Video-game Playing and a Glucose Preload on Food Intake Regulation in Children
The purpose of this experiment is to investigate the effect of active video game playing for 30 minutes on food intake and subjective appetite.
The investigators hypothesize that video game playing will affect food intake in children.
Food intake will be measured at 30 minutes following a glucose (50g glucose in 250ml of water) or sweetened non-caloric (150mg Sucralose® in 250ml of water) beverage with or without active video game playing.
Subjective appetite will be measured at 0, 15, 30 and 60 minutes.
Study Overview
Status
Completed
Conditions
Study Type
Interventional
Enrollment (Actual)
27
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
-
-
Ontario
-
Toronto, Ontario, Canada, M5B 2K3
- School of Nutrition, Ryerson 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
9 years to 14 years (Child)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
healthy boys with no emotional, behavioral or learning problems
Exclusion Criteria:
- Exclusion criteria are children with significant behavioral or emotional difficulties, those with dietary restrictions, or those taking medications.
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: Glucose Beverage
50 g of glucose in solution
|
|
Experimental: Control Beverage
Sucralose in solution
|
|
Experimental: Glucose beverage and active video game playing
50 g of glucose in solution and 30 min of active video game playing
|
|
Experimental: Control Beverage and active video game playing
Sucralose in solution and 30 min of active video game playing
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Food Intake (kcal)
Time Frame: 30 minutes after treatment
|
30 minutes after treatment
|
|
Subjective appetite (mm)
Time Frame: baseline and then 15, 30, and 60 minutes after preload consumption
|
subjective appetite assessed by motivation-to-eat visual analogue scale.
The scale range is between 0 and 100 mm.
Higher scores represent higher appetite
|
baseline and then 15, 30, and 60 minutes after preload consumption
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Subjective Mood (mm)
Time Frame: baseline and then 15, 30, and 60 minutes after preload consumption
|
Measured using visual analogue scale (mm).
Each VAS is a 100 mm line where they will place a pencil mark to describe their feelings.
|
baseline and then 15, 30, and 60 minutes after preload consumption
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 (Actual)
April 6, 2012
Primary Completion (Actual)
May 25, 2015
Study Completion (Actual)
May 25, 2015
Study Registration Dates
First Submitted
October 25, 2018
First Submitted That Met QC Criteria
October 25, 2018
First Posted (Actual)
October 26, 2018
Study Record Updates
Last Update Posted (Actual)
October 29, 2018
Last Update Submitted That Met QC Criteria
October 25, 2018
Last Verified
October 1, 2018
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- REB: 2012-120-1
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
IPD Plan Description
Data will be shared upon request.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
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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