- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03868501
High Working Memory Load to Reduce Internet Gaming Disorder (IGD) Cravings
March 10, 2019 updated by: Jin-tao Zhang, Beijing Normal University
High Working Memory Load to Reduce IGD Cravings: N-Back Task
To test whether high working memory load can effectively reduce the craving for IGD.
Study Overview
Detailed Description
This project is to use 1-back task and 3-back task to reduce the craving of internet gamers.
To test whether high working memory load 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
-
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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 theYoung-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
- Masking: DOUBLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: High Working memory load: n-back task
During the intervention, each participant of this group will finish the 3-back task.
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All participants will be asked to finish the 3-back task and the 1-back task.
The 3-back task and the 1-back task will be carried out at intervals to avoid the influence between different tasks.
The sequence of the 3-back task and the 1-back task will be counterbalanced across participants.
|
|
EXPERIMENTAL: Low Working memory load: n-back task
During the intervention, each participant of this group will finish the 1-back task.
|
All participants will be asked to finish the 3-back task and the 1-back task.
The 3-back task and the 1-back task will be carried out at intervals to avoid the influence between different tasks.
The sequence of the 3-back task and the 1-back task 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
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The craving of internet gamers is measured by a single item Visual Analogue Scale with 1 to 7 likert score.
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0-1 minutes before each set of cue
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The craving of internet gamers after cue
Time Frame: 0-1 minutes after showing cue
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The craving of internet gamers is measured by a single item Visual Analogue Scale with 1 to 7 likert score.
|
0-1 minutes after showing cue
|
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The craving of internet gamers after tasks
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
- Study Director: Jin-Tao Zhang, PhD, Study Principal Investigator
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
- Kaag AM, Goudriaan AE, De Vries TJ, Pattij T, Wiers RW. A high working memory load prior to memory retrieval reduces craving in non-treatment seeking problem drinkers. Psychopharmacology (Berl). 2018 Mar;235(3):695-708. doi: 10.1007/s00213-017-4785-4. Epub 2017 Nov 27.
- 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.
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
- Working memory
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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