NCT07474753

Brief Summary

The impact of caffeine habituation on acute responses to different doses of caffeinated coffee has received minimal attention. This study aimed to investigate the effects of different doses of coffee on physical and cognitive performance in men and women with different levels of daily caffeine consumption. Sixty-nine (35 women) athletes participated in this study, attending 4 experimental visits in a double-blind, randomized, crossover fashion: decaffeinated coffee (PLA), 1.5 mg·kg-1 (LCOF), 3 mg·kg-1 (MCOF) and 6 mg·kg-1 of caffeine (HCOF) from coffee ingestion. Sixty min after coffee consumption, participants performed squat and bench press exercises (1 repetition maximum, 1RM), 60% of 1RM muscular endurance (ME), maximal sprinting, and cognitive performance (CP) was assessed. Participants were allocated into low (LGROUP), moderate (MGROUP), and high (HGROUP) caffeine consumption groups.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
69

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Dec 2020

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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 Start

First participant enrolled

December 4, 2020

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 20, 2021

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 20, 2021

Completed
4.9 years until next milestone

First Submitted

Initial submission to the registry

February 6, 2026

Completed
1 month until next milestone

First Posted

Study publicly available on registry

March 16, 2026

Completed
Last Updated

March 16, 2026

Status Verified

March 1, 2026

Enrollment Period

4 months

First QC Date

February 6, 2026

Last Update Submit

March 11, 2026

Conditions

Outcome Measures

Primary Outcomes (2)

  • Upper- and Lower-boy muscular endurance

    Muscular endurance assessed during bench press and squat exercises using 60% of one-repetition maximum (1RM). Performance expressed as total weight lifted (kg).

    60 minutes after caffeine or placebo ingestion (during each experimental trial)

  • Upper- and lower-body strenght

    Maximal dynamic strength assessed using one-repetition maximum (1RM) tests in the squat and bench press exercises (kg).

    60 minutes after caffeine or placebo ingestion (during each experimental trial)

Secondary Outcomes (2)

  • Sprint Performance

    60 minutes after caffeine or placebo ingestion (during each experimental trial)

  • Cognitive performance

    Baseline (before caffeine ingestion) and 60 minutes after caffeine or placebo ingestion.

Study Arms (4)

Low dose caffeine supplementation

EXPERIMENTAL

consuming 0.12 g·kg-1 of decaffeinated coffee + 0.04 g·kg-1 of caffeinated coffee to achieve 1.5 mg·kg-1 of caffeine intake 60-min before the experimental trial.

Dietary Supplement: Low Dose Caffeine (LCOF)

Moderate dose caffeine supplementation

EXPERIMENTAL

Consuming 0.08 g·kg-1 of decaffeinated coffee + 0.08 g·kg-1 of caffeinated coffee to achieve 3 mg·kg-1 of caffeine intake 60-min before the experimental trial.

Dietary Supplement: Moderate Dose Caffeine (MCOF)

High dose caffeine supplementation

EXPERIMENTAL

Consuming 0.16 g·kg-1 of caffeinated coffee to achieve 6 mg·kg-1 of caffeine intake 60-min before the experimental trial.

Dietary Supplement: High Dose Caffeine (HCOF)

Placebo

EXPERIMENTAL

Consuming 0.16 g·kg-1 of decaffeinated coffee 60-min before the experimental trial.

Dietary Supplement: Placebo (PLA)

Interventions

Low Dose Caffeine (LCOF)DIETARY_SUPPLEMENT

Caffeinated versions of instant coffee were prepared in 600 ml hot water (approximately 65°C) and served in a mug. Participants ingested 0.12 g·kg-1 of decaffeinated coffee + 0.04 g·kg-1 of caffeinated coffee to achieve 1.5 mg·kg-1 of caffeine intake in LCOF 60-min before the experimental trial.

Low dose caffeine supplementation

Caffeinated versions of instant coffee were prepared in 600 ml hot water (approximately 65°C) and served in a mug. Participants ingested 0.08 g·kg-1 of decaffeinated coffee + 0.08 g·kg-1 of caffeinated coffee to achieve 3 mg·kg-1 of caffeine intake in MCOF 60-min before the experimental trial.

Moderate dose caffeine supplementation
High Dose Caffeine (HCOF)DIETARY_SUPPLEMENT

Caffeinated versions of instant coffee were prepared in 600 ml hot water (approximately 65°C) and served in a mug. Participants ingested 0.16 g·kg-1 of caffeinated coffee to achieve 6 mg·kg-1 of caffeine intake in HCOF 60-min before the experimental trial.

High dose caffeine supplementation
Placebo (PLA)DIETARY_SUPPLEMENT

Decaffeinated versions of instant coffee were prepared in 600 ml hot water (approximately 65°C) and served in a mug. Participants ingested 0.16 g·kg-1 of decaffeinated coffee in PLA 60-min before the experimental trial.

Placebo

Eligibility Criteria

Age18 Years - 30 Years
Sexall(Gender-based eligibility)
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Healthy individuals
  • Physically active individuals
  • Non-smokers
  • Age between 18 and 30 years
  • Free from respiratory insufficiency
  • Free from cardiovascular disease
  • Free from neuromuscular disorders
  • Free from musculoskeletal injury within the previous 6 months

You may not qualify if:

  • Diagnosed cardiovascular disease
  • Neuromuscular disease
  • Current limb injury
  • History of limb injury requiring treatment within the previous 6 months
  • Chronic respiratory disease or treatment for chronic respiratory conditions

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ankara University's Department of Sports Science

Ankara, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Motor Activity

Interventions

Caffeine

Condition Hierarchy (Ancestors)

Behavior

Intervention Hierarchy (Ancestors)

XanthinesAlkaloidsHeterocyclic CompoundsPurinonesPurinesHeterocyclic Compounds, 2-RingHeterocyclic Compounds, Fused-Ring

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, INVESTIGATOR
Masking Details
Supplements were allocated in a randomised order and double-blinding design was implemented by an independent technician who did not take part in the study. The randomisation and blinding were held until the end of the study.
Purpose
OTHER
Intervention Model
CROSSOVER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

February 6, 2026

First Posted

March 16, 2026

Study Start

December 4, 2020

Primary Completion

March 20, 2021

Study Completion

March 20, 2021

Last Updated

March 16, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will not share

Locations