Effects of Caffeine and L-Theanine on Physical and Cognitive Performance in Trained Athletes
Acute Effects of Combined and Isolated Caffeine and Theanine Supplementation on Physical and Cognitive Performance in Competitive Athletes: A Randomized, Double-Blind, Placebo-Controlled Crossover Study
1 other identifier
interventional
20
1 country
1
Brief Summary
The aim of this clinical trial is to examine how caffeine and L-theanine, taken alone or together, affect both physical and cognitive performance in healthy, trained athletes. The study aims to answer whether these commonly consumed dietary ingredients can enhance strength, endurance, and hand-eye coordination under controlled laboratory conditions. Researchers will compare four supplementation conditions: Caffeine (CAF) - 3 mg per kilogram of body weight L-Theanine (THE) - 200 mg Combined Caffeine and L-Theanine (COM) - same doses together Placebo (CON) - mannitol (inactive substance) Each participant will complete all four test sessions in a randomized, double-blind, crossover design, with at least 72 hours between sessions. Capsules will be taken 60 minutes before testing to allow time for absorption. During each session, participants will perform a series of physical and cognitive tasks, including maximal isometric strength tests, an intermittent endurance test, and a computerized eye-hand coordination task. The main hypothesis is that caffeine and L-theanine, alone or in combination, will improve strength and cognitive coordination compared with placebo. All participants are healthy competitive athletes between 18 and 30 years old. The study is conducted under standardized laboratory and indoor sports-hall conditions, with ethics approval obtained from the Sinop University Human Research Ethics Committee (Approval No. 2025/337).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Aug 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
August 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 14, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
August 14, 2025
CompletedFirst Submitted
Initial submission to the registry
November 18, 2025
CompletedFirst Posted
Study publicly available on registry
December 8, 2025
CompletedDecember 8, 2025
November 1, 2025
13 days
November 18, 2025
November 25, 2025
Conditions
Outcome Measures
Primary Outcomes (8)
Total Distance Covered in the Yo-Yo Intermittent Endurance Test Level 1 (meters)
Distance (m) completed during the Yo-Yo Intermittent Endurance Test Level 1 following standard protocol.
60 minutes post-supplement ingestion.
Peak Handgrip Force (kgf)
Highest handgrip force obtained from three maximal voluntary contractions using a calibrated digital dynamometer.
60 minutes post-supplement ingestion.
Peak Back Extension Force (kgf)
Highest value from three maximal voluntary contractions measured with a back strength dynamometer.
60 minutes post-supplement ingestion.
Peak Leg Extension Force (kgf)
Highest value from three maximal voluntary contractions measured using a leg dynamometer.
60 minutes post-supplement ingestion.
Eye-Hand Coordination Accuracy (EHC-A)
Accuracy percentage (%) obtained from the computerized eye-hand coordination test battery.
60 minutes post-supplement ingestion.
Eye-Hand Coordination Fast Speed Reaction Time (EHC-FS)
Reaction time (milliseconds) during the fast-speed EHC trial.
60 minutes post-supplement ingestion.
Eye-Hand Coordination Slow Speed Reaction Time (EHC-SS)
Reaction time (milliseconds) during the slow-speed EHC trial.
60 minutes post-supplement ingestion.
Eye-Hand Coordination Distance From Ball Center (EHC-DFBC)
Mean deviation from target center measured during coordination task.
60 minutes post-supplement ingestion.
Study Arms (4)
Caffeine Supplementation (CAF)
EXPERIMENTALParticipants receive 3 mg of anhydrous caffeine per kilogram of body weight, encapsulated in gelatin capsules identical in appearance to other conditions. Capsules are ingested with water 60 minutes before testing.
L-Theanine Supplementation (THE)
EXPERIMENTALParticipants receive 200 mg of L-theanine (pure L-theanine powder, Orzax Pharmaceuticals, Istanbul, Turkey), encapsulated in gelatin capsules identical in appearance to other conditions. Capsules are ingested with water 60 minutes before testing.
Combined Caffeine and L-Theanine (COM)
EXPERIMENTALParticipants receive a combination of 3 mg/kg anhydrous caffeine and 200 mg L-theanine, encapsulated together in identical gelatin capsules. Capsules are taken 60 minutes before testing to assess potential synergistic effects on physical and cognitive performance.
Placebo (CON)
PLACEBO COMPARATORParticipants receive placebo capsules filled with mannitol, a non-nutritive sugar alcohol with no known ergogenic properties. Capsules are identical in size, color, texture, and weight to the active supplement conditions and are ingested 60 minutes before testing.
Interventions
Participants receive 3 mg of anhydrous caffeine per kilogram of body weight, encapsulated in identical gelatin capsules (five in total). Capsules are taken orally with water 60 minutes before testing. The caffeine powder (98.5% purity, Oxford Vitality Health Co., UK) is administered once per experimental session, with at least 72 hours between conditions.
Participants receive a single 200 mg dose of L-theanine (Orzax Pharmaceuticals, Istanbul, Turkey; active ingredient manufactured in Germany) encapsulated in identical gelatin capsules. The supplement is ingested orally with water 60 minutes before testing. All testing sessions are separated by at least 72 hours.
Participants receive a combination of 3 mg/kg anhydrous caffeine and 200 mg L-theanine, encapsulated together in visually identical gelatin capsules. The mixture is taken orally with water 60 minutes before testing to assess potential synergistic effects on performance. Each participant completes all four supplementation conditions in randomized order, separated by ≥72 hours.
Participants receive placebo capsules filled with mannitol, a non-nutritive sugar alcohol with no known ergogenic or ergolytic effects. Capsules are identical in appearance, weight, and texture to the active supplement capsules and are taken orally with water 60 minutes before testing.
Eligibility Criteria
You may qualify if:
- Active participation in individual or team sports at a competitive level
- Age between \[insert range, e.g., 18-30\] years
- Absence of any known medical or metabolic disorder
You may not qualify if:
- History of cardiovascular, neurological, or musculoskeletal disorders within the past 12 months
- Known intolerance or hypersensitivity to caffeine or theanine
- Allergy to mannitol or other excipients used in capsule formulation
- Current use of prescription medications
- Physician-directed restriction of caffeine or theanine consumption.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Sinop University Facility
Sinop, Centarl, 57100, Turkey (Türkiye)
Related Publications (1)
Tuncer SY, Ozdenk S, Yildirim UC, Erkan D, Sari C, Gundem MC, Sar H, Yilmaz B, Karakulak I, Akca F. Acute effects of combined and isolated caffeine and theanine supplementation on physical and cognitive performance in competitive athletes: a randomized, double-blind, placebo-controlled crossover study. Front Nutr. 2026 Jan 26;12:1751673. doi: 10.3389/fnut.2025.1751673. eCollection 2025.
PMID: 41668720DERIVED
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- QUADRUPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- BASIC SCIENCE
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Assoc. Prof.
Study Record Dates
First Submitted
November 18, 2025
First Posted
December 8, 2025
Study Start
August 1, 2025
Primary Completion
August 14, 2025
Study Completion
August 14, 2025
Last Updated
December 8, 2025
Record last verified: 2025-11
Data Sharing
- IPD Sharing
- Will not share