- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03868488
Mental Imagery Tasks to Reduce Internet Gaming Disorder (IGD) Cravings
March 10, 2019 updated by: Jin-tao Zhang
Mental Imagery Tasks to Reduce IGD Cravings: Visual Imagery and Auditory Imagery
To test whether visual and auditory imagery tasks can effectively reduce the craving for IGD.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed Description
This project is to use imagery tasks to reduce the craving of internet gamers.
To test whether visual and auditory imagery tasks can effectively reduce the craving for IGD.
This project will be conducted in Beijing, China, based on a large sample of internet gamers.
Study Type
Interventional
Enrollment (Anticipated)
30
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
-
-
Beijing
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Beijing, Beijing, China, 100875
- State Key Laboratory of Cognitive Neuroscience and Learning, Beijing Normal University
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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
18 years to 30 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- The scores of the 9 items of The Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition(DSM-5) recommended diagnosis for Internet gaming disorder ≥ 5.
- Engagement in popular Internet games (e.g. Arena of Valor, League of Legends and Player Unknown's Battle Grounds) for over 20 hours per week for a minimum of 12 months.
- The scores of the Young-Internet Addiction Test(Y-IAT) ≥ 50
Exclusion Criteria:
- Current or history of use of illegal substances and gambling;
- Current or history of psychiatric or neurological illness;
- Current use of psychotropic 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: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Visual imagery tasks group
During the intervention, each participant of this group will be asked to create visual mental images.
|
All participants need to finish both visual imagery tasks and auditory imagery tasks.
Visual imagery tasks and auditory imagery tasks will be carried out at intervals to avoid the influence of different tasks.
The sequence of imagery tasks will be counterbalanced across participants.
|
|
Experimental: Auditory imagery tasks group
During the intervention, each participant of this group will be asked to create auditory mental images.
|
All participants need to finish both visual imagery tasks and auditory imagery tasks.
Visual imagery tasks and auditory imagery tasks will be carried out at intervals to avoid the influence of different tasks.
The sequence of imagery tasks will be counterbalanced across participants.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The craving of internet gamers
Time Frame: 0-1 minutes before each set of cue
|
The craving of internet gamers is measured by a single item Visual Analogue Scale with 1 to 7 likert score
|
0-1 minutes before each set of cue
|
|
The craving of internet gamers after cue
Time Frame: 0-1 minutes after showing cue
|
The craving of internet gamers is measured by a single item Visual Analogue Scale with 1 to 7 likert scoreScale with 1 to 7 likert score
|
0-1 minutes after showing cue
|
|
The craving of internet gamers
Time Frame: 0-1 minutes after finishing each block of tasks
|
The craving of internet gamers is measured by a single item Visual Analogue Scale with 1 to 7 likert score
|
0-1 minutes after finishing each block of tasks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Jin-Tao Zhang, Phd, Beijing Normal University
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
- May J, Andrade J, Panabokke N, Kavanagh D. Visuospatial tasks suppress craving for cigarettes. Behav Res Ther. 2010 Jun;48(6):476-85. doi: 10.1016/j.brat.2010.02.001. Epub 2010 Feb 7.
- Yates M, Kamboj SK. Alcohol related mental imagery: The effects of a priming dose in at risk drinkers. Addict Behav Rep. 2017 Aug 31;6:71-75. doi: 10.1016/j.abrep.2017.08.003. eCollection 2017 Dec.
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 (Anticipated)
March 10, 2019
Primary Completion (Anticipated)
May 31, 2019
Study Completion (Anticipated)
August 31, 2019
Study Registration Dates
First Submitted
March 1, 2019
First Submitted That Met QC Criteria
March 7, 2019
First Posted (Actual)
March 11, 2019
Study Record Updates
Last Update Posted (Actual)
March 12, 2019
Last Update Submitted That Met QC Criteria
March 10, 2019
Last Verified
March 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Mental imagery tasks
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device 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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