Completed
CHESSPhase I Study About Effects of Caffeine, Methylphenidate, Modafinil and Placebo on Cognitive Performance of Chess Players.
What is being tested
Drugs use: methylphenidate
+ Drug use: modafinil
+ caffeine
Drug
Who is being recruted
From 18 to 60 Years
+9 Eligibility Criteria
How is the trial designed
Services Research Study
Placebo-ControlledPhase 1
Interventional
Study Start: May 2011
Summary
Principal SponsorK. Lieb
Last updated: April 18, 2013
Sourced from a government-validated database.Claim as a partner
Study start date: May 1, 2011
Actual date on which the first participant was enrolled.Effects of caffeine, methylphenidate, modafinil and placebo on cognitive performance of chess players in chess games and neuropsychiatric standardized tests. We hypothesize that substances will change cognitive performance in chess players leading to changed results in chess games and neuropsychiatric tests.
Principal SponsorK. Lieb
Last updated: April 18, 2013
Sourced from a government-validated database.Claim as a partner
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.Design Details
40 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Services Research Study
These studies look at how healthcare is delivered, managed, and organized. They aim to improve care quality, patient experience, and access to treatment.
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Criteria
Male
Biological sex of participants that are eligible to enroll.From 18 to 60 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Criteria
3 inclusion criteria required to participate
18-60 years old
existence of ELO-number
male
6 exclusion criteria prevent from participating
addiction of psychoactive substances
irregular day-night-rhythm (e.g. shift workers)
physical diseases (e.g. diabetes mellitus, etc.) with necessity of using prescription drugs
psychiatric diseases (e.g. psychosis, bipolar disorders, etc.) with necessity of using prescription drugs
Show More Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Treatment Groups
Study Objectives
4 intervention groups are designated in this study
25% chance of being blinded to the placebo group
Treatment Groups
Group I
ExperimentalMethylphenidate
Group II
Experimentalmodafinil
Group III
Experimentalcaffeine
Group IV
Placeboplacebo
Study Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Department of Psychiatry and Psychotherapy
Mainz, GermanyOpen Department of Psychiatry and Psychotherapy in Google MapsCompletedOne Study Center