NCT07530185

Brief Summary

Participants will complete five sessions, including one familiarization and baseline session and four experimental conditions (placebo, L-tyrosine, caffeine, and combined supplementation). The baseline session will include resting measurements. The experimental conditions will be performed in a randomized, counterbalanced crossover design with a washout period of at least 72 hours between sessions.

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
18

participants targeted

Target at below P25 for not_applicable

Timeline
10mo left

Started Apr 2026

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress5%
Apr 2026Mar 2027

First Submitted

Initial submission to the registry

April 1, 2026

Completed
Same day until next milestone

Study Start

First participant enrolled

April 1, 2026

Completed
14 days until next milestone

First Posted

Study publicly available on registry

April 15, 2026

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2026

Expected
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2027

Last Updated

April 15, 2026

Status Verified

April 1, 2026

Enrollment Period

8 months

First QC Date

April 1, 2026

Last Update Submit

April 8, 2026

Conditions

Keywords

L-tyrosineCaffeineBoxingBDNFCognitive performanceAnaerobic performance

Outcome Measures

Primary Outcomes (1)

  • Stroop Test Performance

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

    up to 12 weeks

Secondary Outcomes (2)

  • BDNF Levels

    up to 12 weeks

  • Oxidative Stress Markers

    up to 12 weeks

Study Arms (4)

Placebo

PLACEBO COMPARATOR

Participants receive placebo condition.

Dietary Supplement: Placebo

L-tyrosine

EXPERIMENTAL

Participants receive L-tyrosine condition.

Dietary Supplement: L-Tyrosine

Caffeine

EXPERIMENTAL

Participants receive caffeine condition.

Dietary Supplement: Caffeine

Combined

EXPERIMENTAL

Participants receive combined supplementation condition.

Dietary Supplement: L-tyrosine + Caffeine

Interventions

PlaceboDIETARY_SUPPLEMENT

Placebo solution matched in taste and volume to active supplements.

Placebo
L-TyrosineDIETARY_SUPPLEMENT

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

L-tyrosine
CaffeineDIETARY_SUPPLEMENT

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

Caffeine
L-tyrosine + CaffeineDIETARY_SUPPLEMENT

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

Combined

Eligibility Criteria

Age18 Years+
Sexmale(Gender-based eligibility)
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ataturk University Faculty of Sport Sciences

Erzurum, Turkey (Türkiye)

Location

MeSH Terms

Interventions

TyrosineCaffeine

Intervention Hierarchy (Ancestors)

Amino Acids, AromaticAmino Acids, CyclicAmino AcidsAmino Acids, Peptides, and ProteinsXanthinesAlkaloidsHeterocyclic CompoundsPurinonesPurinesHeterocyclic Compounds, 2-RingHeterocyclic Compounds, Fused-Ring

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, INVESTIGATOR
Masking Details
Both participants and investigators are blinded to the supplementation conditions. Supplements are prepared and coded by an independent researcher to ensure double-blind conditions.
Purpose
BASIC SCIENCE
Intervention Model
CROSSOVER
Model Details: Participants will complete four experimental conditions (placebo, L-tyrosine, caffeine, and combined supplementation) in a randomized, counterbalanced crossover design with a washout period of at least 72 hours between sessions.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Research Assistant and PhD Student

Study Record Dates

First Submitted

April 1, 2026

First Posted

April 15, 2026

Study Start

April 1, 2026

Primary Completion (Estimated)

December 1, 2026

Study Completion (Estimated)

March 1, 2027

Last Updated

April 15, 2026

Record last verified: 2026-04

Data Sharing

IPD Sharing
Will not share

Locations