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Not yet recruitingNCT07530185TYCAF-BOXUpdated Jul 8, 2026

Effects of L-Tyrosine and Caffeine on Performance in Elite Boxers

An interventional study of Placebo and L-Tyrosine in Sports Performance, sponsored by Inonu University. Not yet recruiting at 1 site in Turkey (Türkiye). Open to male participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-07-08.

Sponsored by Inonu University · Not applicable, Interventional, and Basic science

Phase
Not applicable
Study type
Interventional
Enrollment
18
Allocation
Randomized
Ages
18 Years and older
Sex
Male
01

Study summary

Participants will complete six sessions, including one familiarization and baseline session followed by five experimental conditions: control (no supplementation), placebo, L-tyrosine, caffeine, and combined L-tyrosine plus caffeine. The experimental conditions will be performed in a randomized, counterbalanced crossover design with a washout period of at least 72 hours between sessions. Resting physiological and cognitive assessments will be performed during the familiarization session, while biochemical, cognitive, and boxing-specific performance assessments will be conducted before and after each experimental session.

Read the detailed description

Participants will attend six sessions in total. The first session will be used for familiarization and baseline assessments, including anthropometric measurements, resting physiological measurements, and cognitive performance testing. The remaining five sessions will consist of one control condition (no supplementation) and four randomized experimental conditions (placebo, L-tyrosine, caffeine, and combined L-tyrosine plus caffeine) administered in a randomized, counterbalanced crossover design.

Each experimental session will be separated by a washout period of at least 72 hours. During the placebo, L-tyrosine, caffeine, and combined supplementation conditions, the assigned intervention will be administered 60 minutes before exercise. No supplement will be administered during the control condition.

Before and immediately after each experimental session, venous blood samples will be collected to assess brain-derived neurotrophic factor (BDNF) and oxidative stress biomarkers, including total antioxidant status (TAS), total oxidant status (TOS), malondialdehyde (MDA), superoxide dismutase (SOD), and glutathione peroxidase (GPx). Cognitive performance will be evaluated using the computerized Stroop test, and boxing-specific physical performance will be assessed using a standardized boxing simulation protocol. Heart rate and rating of perceived exertion (RPE) will also be recorded during the exercise protocol.

02

Conditions studied

  • Sports Performance

Keywords

  • L-tyrosine
  • Caffeine
  • Boxing
  • BDNF
  • Cognitive performance
  • Anaerobic performance
03

In context

Lead sponsor

Inonu University is the lead sponsor of 375 studies on the registry; 86 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Male
Accepts healthy volunteers
Yes

Inclusion criteria

Male elite boxers aged ≥18 years At least 8 years of boxing training experience Active participation in national or international competitions Regular training schedule No injury or illness affecting performance

Exclusion criteria

Exclusion Criteria:

Use of nutritional supplements or stimulants within the last 4 weeks Any cardiovascular, metabolic, or neurological disorder Current injury or musculoskeletal limitation Smoking or excessive caffeine intake Failure to comply with study procedures

05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Double (Participant, Investigator)
Enrollment
18 participants (estimated)

Study arms

  • Placebo comparator
    Placebo

    Participants receive placebo condition.

    Dietary Supplement: Placebo

  • Experimental
    L-tyrosine

    Participants receive L-tyrosine condition.

    Dietary Supplement: L-Tyrosine

  • Experimental
    Caffeine

    Participants receive caffeine condition.

    Dietary Supplement: Caffeine

  • Experimental
    Combined

    Participants receive combined supplementation condition.

    Dietary Supplement: L-tyrosine + Caffeine

  • No intervention
    Control

    Participants complete the experimental protocol without receiving placebo or active supplementation. Baseline cognitive, physiological, and physical performance assessments are performed under the control condition.

Interventions

  • Dietary supplementPlacebo

    Placebo solution matched in taste and volume to active supplements.

  • Dietary supplementL-Tyrosine

    L-tyrosine at 150 mg/kg body weight administered 60 minutes before exercise.

  • Dietary supplementCaffeine

    Caffeine at 5 mg/kg body weight administered 60 minutes before exercise.

  • Dietary supplementL-tyrosine + Caffeine

    Combined L-tyrosine (150 mg/kg) and caffeine (5 mg/kg) administered 60 minutes before exercise.

06

What researchers measure

Primary outcomes

  1. Stroop Test Performance

    Cognitive performance assessed using the Stroop test, including reaction time and accuracy.

    Time frame: up to 12 weeks

Secondary outcomes

  1. BDNF Levels

    Serum brain-derived neurotrophic factor levels measured before and after exercise.

    Time frame: up to 12 weeks

  2. Oxidative Stress Markers

    Serum levels of total antioxidant status (TAS), total oxidant status (TOS), malondialdehyde (MDA), superoxide dismutase (SOD) activity, and glutathione peroxidase (GPx) activity will be measured.

    Time frame: up to 12 weeks

07

Study locations

1 site
  • Ataturk University Faculty of Sport Sciences
    Erzurum, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 8, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07530185
Lead sponsor
Inonu University
Collaborators
Ataturk University
Responsible party
Halil UÇAR (Research Assistant and PhD Student, Inonu University) — Principal investigator
First posted
Apr 15, 2026
Start date
Sep 2026 (estimated)
Primary completion
Dec 2026 (estimated)
Completion
Mar 2027 (estimated)
Last update
Jul 8, 2026

Study contacts

Halil UÇAR
Contact
halil.ucar@inonu.edu.tr
+90 5462921133

Oversight

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

Not currently enrolling

This study is not yet recruiting, as verified in Jul 2026. You cannot join it, but the record below documents what was studied.

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