- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02281825
Correlating Real and Virtual World Behavioral Fluctuations in Adolescence
April 13, 2016 updated by: Shalvata Mental Health Center
The present study will explore a new approach to ongoing evaluation and monitoring of fluctuations in personality traits via commercial video games.
The aim of this longitudinal study is to examine the influence of everyday life event on video games performance as a function of individual differences in gaming behavioral patterns.
focusing on the ongoing performance vacillations of the patient on commercial video games will offer insights in to possibly new generation of real time assessment medium of ongoing behavior.
Study Overview
Status
Completed
Study Type
Observational
Enrollment (Actual)
20
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
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Hod Hasharon, Israel
- Shalvata MHC
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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
13 years to 18 years (Child, Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Male
Sampling Method
Non-Probability Sample
Study Population
Male adolescents, 13-18, with and without psychopathology, evaluated and diagnosed by psychiatrists.
Adolescents will be recruited from Shalvata MHC children and adolescents outpatient clinic and from convinience sample in the community.
Description
Inclusion Criteria:
- All subjects will have normal or corrected to normal vision with no sensory/motor disturbance
- An accessible computer at the house hold
- Previous experience in playing computer games.
Exclusion Criteria:
- drug abuse
- head injury
- living in a boarding school and a major psychiatric or neurological disorder.
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
Cohorts and Interventions
Group / Cohort |
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Control
Adolescents without any psychiatric disorder
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Study
Adolescents with psychiatric disorder of the following: Attention-Deficit and Hyperactivity Disorder, Conduct, Oppositional defiant Disorder, Anxiety, Depression, Disruptive Mood Dysregulation Disorder
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Impulsivity manifested within game-play
Time Frame: 3 weeks
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In-Game kill/Stealth ratio
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3 weeks
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Activity manifested within game-play
Time Frame: 3 weeks
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In-Game number of missions and sub-mission attained
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3 weeks
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Aggresion manifested within game-play
Time Frame: 3 weeks
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In-Game aimed killing
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3 weeks
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Aviv Segev, MD, Shalvata MHC, Sackler Faculty of Medicine, TA Uni.
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
November 1, 2014
Primary Completion (Actual)
December 1, 2015
Study Completion (Actual)
February 1, 2016
Study Registration Dates
First Submitted
October 29, 2014
First Submitted That Met QC Criteria
November 3, 2014
First Posted (Estimate)
November 4, 2014
Study Record Updates
Last Update Posted (Estimate)
April 14, 2016
Last Update Submitted That Met QC Criteria
April 13, 2016
Last Verified
April 1, 2016
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- sha-0001-14
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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