- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01809470
Metabolic Response to Playing Video Games
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Our study is investigating the metabolic response to playing competitive non-violent and competitive violent video games. Our primary hypothesis is that the metabolic response in the violent game group will differ from the other two groups, due to activation of the stress response.
We are using an experimental approach, whereby 72 young men are randomised to one of three groups: watching TV, playing the non-violent video game 'FIFA2013', or playing the violent video game 'Call of Duty'. All participants must already have some experience playing the two games, so that whichever group they are assigned to, they can comply with the protocol.
Participants arrive after an overnight fast, and are given a standardised breakfast (a muffin, approx 300 kcal, and a glass of water). After measurements of weight, height and waist girth, they then are assigned to one of the three groups, and allowed to familiarise themselves with the games console or TV. Baseline data on blood pressure (in triplicate, Accutor digital monitor), heart rate (Polar monitor) and appetite/mood (visual analogue scale) are collected, along with a saliva sample for measurement of the 'stress' hormone, cortisol, as well as satiety hormones sich as leptin and ghrelin. We will collect these data again at 4 time-points during the one hour game-playing session, by pausing the game or TV for 4 minutes at 15, 30, 45 and 60 minutes after the session starts.
At the end of the study, we allow the participants half an hour of rest, during which they can choose from a variety of sweet or savoury snacks or fruit, and several drinks.
We will compare the data from the three groups, to test whether changes in blood pressure, heart rate, appetite/mood and salivary hormones, as well as snack consumption, are greater in the group playing the violent game.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
London, United Kingdom, WC1N 1EH
- Recruiting
- UCL Institute of Child Health
-
Contact:
- Jonathan C Wells, PhD
- Phone Number: +442079052389
- Email: Jonathan.Wells@ucl.ac.uk
-
Principal Investigator:
- Jonathan C Wells, PhD
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- BMI >25 kg/m2
Exclusion Criteria:
- smoker
- weight change >3 kg in the previous three months
- psychiatric disorder
- uncontrolled hypertension
- coronary heart disease, heart failure and central or peripheral arteriopathies
- alcohol consumption > 21 units/week.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Watching TV
Watching TV (comedy, 'Friends') for 1 hour
|
Watching TV for 1 hour
|
|
Experimental: FIFA2013
Playing the video game 'FIFA2013' for 1 hour
|
Playing FIFA2013 for 1 hour
|
|
Experimental: Call of Duty
Playing the video game 'Call of duty' for 1 hour
|
Playing Call of Duty for 1 hour
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Blood pressure
Time Frame: Over the 90 minutes of the study
|
Systolic and diastolic blood pressure
|
Over the 90 minutes of the study
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Heart rate
Time Frame: Over the 90 minute duration of the study
|
Heart rate by Polar monitor
|
Over the 90 minute duration of the study
|
|
Appetite
Time Frame: Over the 90 minute duration of the study
|
Appetite by visual analogue scale, and by a test meal at the end of the study
|
Over the 90 minute duration of the study
|
|
Stress
Time Frame: Over the 90 minute duration of the study
|
Salivary cortisol
|
Over the 90 minute duration of the study
|
|
Satiety
Time Frame: Over the 90 minute duration of the study
|
Salivary ghrelin and leptin
|
Over the 90 minute duration of the study
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Jonathan C Wells, PhD, UCL Institute of Child Health
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- UCL-VG-001
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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