ClinicalTrials.gg
RecruitingNCT07641335GRANDMASTERUpdated Sep 30, 2026

Effects of Caffeine on Chess Performance and Cognitive Function in Professional Chess Players

An interventional study of Caffeinated Coffee and Decaffeinated Coffee Placebo in Cognitive Performance, Attention and Reaction Time, sponsored by St. Louis University. Recruiting at 1 site in United States. Open to participants aged 18 Years to 50 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-30.

Sponsored by St. Louis University · Not applicable, Interventional, and Basic science

From the registry’s dates

  • Started Aug 2026; still recruiting 2 months later.
Updated Sep 30, 2026Now RecruitingSite recruiting status changed+2 moreGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
12
Allocation
Randomized
Ages
18 Years to 50 Years
Sex
All
01

Study summary

This study will examine whether caffeine improves cognitive and competitive performance in professional chess players during tournament-style games. In a randomized double-blind crossover design, participants will complete two experimental sessions in which they consume either caffeinated coffee or decaffeinated coffee before playing a standardized chess match. Cognitive performance will be assessed using attention and reaction-time tests, including the Stroop Test, Trail Making Test, and Puzzle Rush task. Chess performance outcomes such as move accuracy, time management, and error rates will also be evaluated. The study aims to determine whether moderate caffeine intake enhances focus, alertness, and decision-making during prolonged competitive chess play.

Read the detailed description

This randomized double-blind crossover trial will evaluate the effects of moderate caffeine intake on cognitive and competitive performance in professional chess players. Twelve FIDE-rated chess players will complete two experimental conditions in randomized order: caffeinated coffee and decaffeinated coffee placebo. During each visit, participants will complete standardized cognitive assessments and a tournament-style chess game under controlled laboratory conditions.

Primary outcomes will include objective chess performance metrics derived from chess engine analysis, including move accuracy, centipawn loss, error rates, and time management. Secondary outcomes will include cognitive test performance, tactical reaction time, and self-reported alertness and fatigue. Chess games will be analyzed using standardized software-based evaluation methods.

The crossover design allows each participant to serve as their own control, minimizing variability related to individual differences in skill level, caffeine tolerance, and playing style. The study aims to determine whether caffeine enhances sustained attention, decision-making, and competitive chess performance during prolonged gameplay. Findings may provide insight into nutritional strategies for cognitive performance optimization in mentally demanding competitive environments.

02

Conditions studied

  • Cognitive Performance
  • Attention
  • Reaction Time
  • Caffeine

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Keywords

  • Caffeine
  • Chess Performance
  • Cognitive Performance
  • Attention
  • Mental Fatigue
  • Professional Chess Players
  • Decision Making
  • Neurocognitive Performance
  • Randomized Crossover Trial
  • Coffee
  • Alertness
  • Executive Function
  • Cognitive Fatigue
03

In context

Mental Fatigue

175 studies on the registry are indexed under Mental Fatigue; 54 are open to participants now.

This study's planned enrollment of 12 is below the median of 45 across 143 interventional studies indexed under Mental Fatigue.

Browse Mental Fatigue studies →

Lead sponsor

St. Louis University is the lead sponsor of 156 studies on the registry; 17 are open to participants now.

Of its 19 completed or terminated interventional studies of FDA-regulated products, 15 (79%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 50 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Male and female professional chess players aged 18-50 years
  • Current Fédération Internationale des Échecs (FIDE) standard rating between 2300 and 2600 Elo, or achievement of a standard FIDE rating within this range during the previous 12 months
  • Habitual caffeine consumers consuming ≤2 cups of coffee per day
  • Willingness to comply with all study procedures and study visits
  • Ability to provide written

Exclusion criteria

Exclusion Criteria:

  • Non-caffeine users
  • Habitual caffeine intake exceeding 2 cups of coffee per day
  • Cardiovascular disorders
  • Metabolic disorders
  • Psychiatric disorders
  • Pregnancy or breastfeeding
  • Current smoking
  • Shift workers
  • Use of psychoactive medications
  • Participation in another clinical trial within the previous 3 months
  • Known allergy or intolerance to milk proteins, dairy products, or soy
  • Known red-green color blindness or other color vision deficiencies that may interfere with Stroop Test performance
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Triple (Participant, Investigator, Outcomes assessor)
Enrollment
12 participants (estimated)

Study arms

  • Active comparator
    Caffeinated Coffee

    Participants will consume one serving of black caffeinated coffee prepared from 15 g of ground coffee brewed in 200 g of water, providing approximately 100 mg of caffeine. The beverage will be consumed approximately 30 minutes before completion of cognitive testing and a standardized tournament-style chess game during the experimental visit.

    Dietary Supplement: Caffeinated Coffee

  • Placebo comparator
    Decaffeinated Coffee Placebo

    Participants will consume one serving of black decaffeinated coffee prepared to match the caffeinated coffee in taste and appearance. The beverage will be consumed approximately 30 minutes before completion of cognitive testing and a standardized tournament-style chess game during the experimental visit.

    Dietary Supplement: Decaffeinated Coffee Placebo

Interventions

  • Dietary supplementCaffeinated Coffee

    Black caffeinated coffee prepared from 15 g of ground coffee brewed in 200 g of water, providing approximately 100 mg of caffeine. The beverage will be consumed approximately 30 minutes before cognitive testing and tournament-style chess gameplay.

  • Dietary supplementDecaffeinated Coffee Placebo

    Black decaffeinated coffee prepared from the same batch of coffee beans and matched for taste and appearance to the caffeinated condition. The beverage will be consumed approximately 30 minutes before cognitive testing and tournament-style chess gameplay.

06

What researchers measure

Primary outcomes

  1. Chess Performance Accuracy

    Chess performance accuracy will be assessed using engine-based analysis of tournament-style chess games. The primary reported metric will be average centipawn loss per move, with lower values indicating better chess performance accuracy.

    Time frame: 30 minutes after beverage consumption through completion of the tournament-style chess game at each experimental visit.

Secondary outcomes

  1. Puzzle Rush Correct Responses

    Tactical accuracy will be assessed using the 3-minute Puzzle Rush task on Chess.com. The outcome will be the total number of correctly solved tactical puzzles, with higher scores indicating better tactical accuracy.

    Time frame: Approximately 30 minutes after beverage consumption at each experimental visit.

  2. Puzzle Rush Response Speed

    Response speed will be assessed using the 3-minute Puzzle Rush task on Chess.com. The outcome will be average response time per puzzle, with lower values indicating faster response speed.

    Time frame: Approximately 30 minutes after beverage consumption at each experimental visit.

  3. Stroop Test Performance

    Selective attention will be assessed using the Stroop Test. The outcome will be the change in Stroop Test completion time from before gameplay to immediately after gameplay, with lower completion time indicating better performance.

    Time frame: Before gameplay and immediately after gameplay at each experimental visit.

  4. Trail Making Test Performance

    Cognitive flexibility and processing speed will be assessed using the Trail Making Test. The outcome will be the change in Trail Making Test completion time from before gameplay to immediately after gameplay, with lower completion time indicating better performance.

    Time frame: Before gameplay and immediately after gameplay at each experimental visit.

  5. Self-Reported Alertness

    Self-reported alertness will be assessed using a study-specific visual analog questionnaire. Higher scores will indicate greater perceived alertness.

    Time frame: Pre-game and immediately post-game at each experimental visit.

  6. Self-Reported Mental Fatigue

    Self-reported mental fatigue will be assessed using a study-specific visual analog questionnaire. Higher scores will indicate greater perceived mental fatigue.

    Time frame: Pre-game and immediately post-game at each experimental visit.

  7. Average Time Per Move

    Chess time management will be assessed as the average time used per move during each tournament-style chess game. This value will be calculated from the total game time divided by the number of moves completed by the participant.

    Time frame: From the start of the tournament-style chess game until game completion, assessed over approximately 3 to 4 hours at each experimental visit.

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: No — Individual participant data (IPD) will not be publicly shared because this is a small pilot study involving highly specialized professional chess players, and there is potential risk of participant identification despite de-identification procedures.

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Status
Not yet recruiting→Recruiting
changed Sep 30, 2026
Sites
Saint Louis University is now Recruiting
Sep 30, 2026
Start date
Jun 15, 2026→Aug 25, 2026 (actual)
Sep 30, 2026
Primary completion
Jun 2027→Jul 30, 2027
Sep 30, 2026
Site contacts
Changed at 1 site. See the sites
Show the site
  • Saint Louis University · St Louis, United StatesContact •••8675→•••8675
Sep 30, 2026
Show all 1 update
  1. Sep 30, 2026
    Not yet recruiting→Recruiting
    Saint Louis University is now Recruiting
    Start date Jun 15, 2026→Aug 25, 2026 (now actual)
    Primary completion Jun 2027→Jul 30, 2027
    Site contacts Changed at 1 site. See the sites
    Show the site
    • Saint Louis University · St Louis, United StatesContact •••8675→•••8675

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07641335
Responsible party
Hossein Rafiei (Assistant Professor, St. Louis University) — Principal investigator
First posted
Jun 11, 2026
Start date
Aug 25, 2026
Primary completion
Jul 30, 2027 (estimated)
Completion
Aug 30, 2027 (estimated)
Last update
Sep 30, 2026

Study contacts

Hossein Rafiei, PhD
Contact
hossein.rafiei@health.slu.edu
13149778675
Hossein Rafiei, PhD
principal investigator · St. Louis University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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