- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06346353
Substance Consumption, Personality, and Cognitive Functioning of Chess Players
April 28, 2025 updated by: Central Institute of Mental Health, Mannheim
Substance Consumption, Personality, and Cognitive Functioning of Chess Players and Non-chess Players - an Online Survey
The aim of this project is to find out if there is a difference in addictive behavior, personality traits, and cognitive abilities between chess players and non-chess players.
Study Overview
Status
Completed
Conditions
Detailed Description
In the present planned study, tournament chess players will be compared with non-tournament chess playing individuals by means of an online survey.
Among other things, the investigators want to investigate whether these groups of persons differ in various characteristics such as their consumption behavior (alcohol, tobacco, and drug use), their personality, their depressiveness and mood, or their cognitive abilities.
The background is the question whether playing chess could be protective against substance use disorders or could mitigate the manifestation.
Study Type
Observational
Enrollment (Actual)
756
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
-
-
-
Mannheim, Germany
- Klinik für Abhängiges Verhalten, Zentralinstitut für Seelische Gesundheit
-
-
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
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
The survey is aimed at people who are at least 18 years old.
There is no upper age limit.
There is a division into two groups.
Firstly, people who play chess in a club and have a DWZ (German rating).
Secondly, there is a comparison group of people who do not play chess or only play chess as a hobby and therefore do not have a DWZ.
Description
Inclusion Criteria:
- all persons from the age of 18 years
- Inclusion in the group of chess players is based on the existence of a DWZ.
- Sufficient ability to answer the questionnaires
Exclusion Criteria:
- None
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 |
|---|
|
Chess players
Chess players who play tournament chess and have a DWZ (deutsche Wertungszahl) and/or ELO rating
|
|
Non-chess players
Non-chess players or hobby chess players who do not have a DWZ or ELO rating
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Substance Craving
Time Frame: baseline
|
Mannheimer Craving Scale (MACS), Nakovics, Diehl, Geiselhart, & Mann, 2009
|
baseline
|
|
Alcohol Use
Time Frame: baseline
|
Alcohol Use Disorders Indentification Scale (AUDIT-C), Bohn, Babor, & Kranzler, 1995
|
baseline
|
|
Automatic Alcohol Craving
Time Frame: baseline
|
Craving Automated Scale - Alcohol (CAS-A), Vollstädt-Klein, Leménager, Jorde, Kiefer, & Nakovics, 2015
|
baseline
|
|
Severity of Nicotine Dependence
Time Frame: baseline
|
Fagerstrom Test of Nicotine Dependence (FTND), Heatherton, Kozlowski, Frecker, & Fagerström, 1991
|
baseline
|
|
Automatic Cigarette Craving
Time Frame: baseline
|
Craving Automated Scale - Cigarette Smoking (CAS-CS), Tan et al., 2022
|
baseline
|
|
Smoking Consequences
Time Frame: baseline
|
Smoking Consequences Questionnaire (SCQ), Lewis-Esquerre, Rodrigue, & Kahler, 2005
|
baseline
|
|
Drug Abuse
Time Frame: baseline
|
Drug Abuse Screening Test (DAST-10), Lam et al., 2015
|
baseline
|
|
Personality
Time Frame: baseline
|
NEO five factor inventory (NEO-FFI), Körner et al., 2008
|
baseline
|
|
Depression
Time Frame: baseline
|
Beck Depressions Inventar - II (BDI-II) Kühner, Bürger, Keller, & Hautzinger, 2007
|
baseline
|
|
Anxiety
Time Frame: baseline
|
State Trait Anxiety Inventory (STAI - trait Version), Spielberger, 1983
|
baseline
|
|
self-efficacy
Time Frame: baseline
|
Self-efficacy expectancy (SWE) Jerusalem & Schwarzer, 1999
|
baseline
|
|
coping with stress
Time Frame: baseline
|
Brief COPE, Carver, Scheier, & Weintraub, 1989
|
baseline
|
|
Inhibition capacity
Time Frame: baseline
|
Stop Signal Task (Sebastian et al., 2013)
|
baseline
|
|
Working Memory capacity
Time Frame: baseline
|
N-back Task (Charlet et al., 2014)
|
baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Sabine Vollstädt-Klein, Prof. Dr., Central Institute of Mental Health, Mannheim
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 (Actual)
January 31, 2024
Primary Completion (Actual)
May 31, 2024
Study Completion (Actual)
May 31, 2024
Study Registration Dates
First Submitted
February 2, 2023
First Submitted That Met QC Criteria
March 28, 2024
First Posted (Actual)
April 4, 2024
Study Record Updates
Last Update Posted (Actual)
May 1, 2025
Last Update Submitted That Met QC Criteria
April 28, 2025
Last Verified
April 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Chess Cognition SUD
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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