- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04674436
Can a 6-minute Walking or Resting Break Improve Executive Function in Gamers.
Can a 6-minute Walking or Resting Break Improve Executive Function and Gaming
Study Overview
Detailed Description
A ranked first person shooter player will play for two hours each session, and on separate days will take a 6 minute walking break or a 6 minute resting break within 2 hours of game play. This study is virtual and you may play from your regular home gaming computer. The third day will be continuous play.
The study will take place on 3 separate days. Preferably 2 -3 days in -between testing days.
- Participants will sign an electronic consent form to sign and agree to participate. It will explain the study in detail.
- Participants will then be asked to take two executive function tests online. These test will be sent electronically through email. This is for practice. These tests take approximately 6-7 minutes.
- We will schedule one day where the participant will play a first -person shooter game. Prior to playing the participants will be take to take the two executive function tests.
- On one day the participant will be asked to stop after the first hour (they will be allowed to finish the test) they will either walk for 6 minutes near their computer or rest for 6 minutes. Participants will be contacted through cell phones or discord.
- Game play will resume normally for another hour. When that hour is completed the participant will be asked to take the two online tests again.
- This will be 2 days. The third day the participant will take the online tests and play continuous for 2 hours with no break and then repeat the online tests.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
New York
-
Old Westbury, New York, United States, 11568
- New York Institute of Technology College of Osteopathic Medicine
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Old Westbury, New York, United States, 11758
- New York Institute of Technology
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:1. Women or men 18-25 years of age 2. Play first-person shooter games with a ranking of "gold" or higher (self reported).
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Exclusion Criteria:1. Any participants that do not have a competitive ranking 2. Any participants that are colorblind (self reported) 3. Any participants that have sustained previous hand injuries within the last year, or suffer from chronic wrist pain.
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Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: 6 minute walking break
Participants will walk casually for 6 minutes following one hour of game play, then continue play for one more hour.
|
6 minute casual walk
|
|
Experimental: 6 minute rest break
Participants will rest supine for 6 minutes following one hour of game play, then continue play for one more hour.
|
6 minute casual walk
|
|
No Intervention: Continuous play
Participants will play continuous for 2 hours.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Executive Function
Time Frame: 2 hours
|
The primary purpose of this study is to evaluate executive function changes following a 6-minute walking break to a 6 minute resting break in competitive esport players following 60 minutes of prolonged play
|
2 hours
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Joanne Donoghue, New York Institute of Technology
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- BHS-1566
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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