NCT07830459

Brief Summary

This study compares the effects of acute (single-session) and short-term (7-day) consumption of different doses of caffeine (3 and 6 mg/kg) on maximal strength, strength endurance, vertical jump, and medicine ball throw performance in habitual caffeine-consuming women (daily intake of 5 mg/kg). Thirty-six resistance-trained women were randomly assigned to three groups: 3 mg/kg caffeine, 6 mg/kg caffeine, or placebo in a double-blind crossover design. Participants completed both acute (60 min pre-exercise) and short-term (7 consecutive days) protocols. The main findings showed that acute ingestion of 6 mg/kg caffeine impaired peak power in the maximal strength test, while short-term consumption of the same dose improved peak power in the strength-endurance test. The 3 mg/kg dose was ineffective in all conditions. Caffeine did not affect jump or throw performance. The study highlights the need for individualized caffeine guidelines based on timing, dosage, and habituation status.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
36

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Feb 2023

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

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 12, 2023

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 20, 2023

Completed
10 days until next milestone

Study Completion

Last participant's last visit for all outcomes

March 30, 2023

Completed
3.5 years until next milestone

First Submitted

Initial submission to the registry

September 15, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

September 21, 2026

Completed
Last Updated

September 21, 2026

Status Verified

September 1, 2026

Enrollment Period

1 month

First QC Date

September 15, 2026

Last Update Submit

September 15, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Change in Peak Power (PP) During Maximal Strength Test

    Peak concentric power (Watts) during 1-RM bench press test, measured using a validated Kinect camera

    Baseline, 60 minutes post-ingestion (acute), and after 7 days of supplementation (short-term)

Secondary Outcomes (4)

  • Change in Peak Power During Strength-Endurance Test

    Baseline, 60 minutes post-ingestion (acute), and after 7 days of supplementation (short-term)

  • Change in Medicine Ball Throw Distance

    Baseline, 60 minutes post-ingestion (acute), and after 7 days of supplementation (short-term)

  • Change in Vertical Jump Height

    Baseline, 60 minutes post-ingestion (acute), and after 7 days of supplementation (short-term)

  • Change in Number of Repetitions (Strength-Endurance)

    Baseline, 60 minutes post-ingestion (acute), and after 7 days of supplementation (short-term)

Study Arms (3)

Caffeine 3 mg/kg

EXPERIMENTAL

Participants received 3 mg/kg body weight of caffeine powder in gelatin capsules daily for 7 days. Acute consumption: 60 minutes before testing. Short-term consumption: 7 consecutive days

Dietary Supplement: Caffeine 3 mg/kg

Caffeine 6 mg/kg

EXPERIMENTAL

Participants received 6 mg/kg body weight of caffeine powder in gelatin capsules daily for 7 days. Acute consumption: 60 minutes before testing. Short-term consumption: 7 consecutive days

Dietary Supplement: Caffeine 6 mg/kg

Placebo

PLACEBO COMPARATOR

Participants received identical capsules containing flour, consumed daily for 7 days

Dietary Supplement: Placebo

Interventions

Caffeine 3 mg/kgDIETARY_SUPPLEMENT

Caffeine powder (99% purity) encapsulated in gelatin capsules at a dose of 3 mg per kilogram of body weight. The capsules are identical in appearance, odor, and taste to the placebo. Participants consume the capsules daily for 7 consecutive days. On the testing day, the capsules are ingested 60 minutes prior to the exercise tests.

Caffeine 3 mg/kg
Caffeine 6 mg/kgDIETARY_SUPPLEMENT

Caffeine powder (99% purity) encapsulated in gelatin capsules at a dose of 6 mg per kilogram of body weight. The capsules are identical in appearance, odor, and taste to the placebo. Participants consume the capsules daily for 7 consecutive days. On the testing day, the capsules are ingested 60 minutes prior to the exercise tests.

Caffeine 6 mg/kg
PlaceboDIETARY_SUPPLEMENT

Placebo capsules containing inert flour (or microcrystalline cellulose), identical in appearance, odor, and taste to the caffeine capsules. Participants consume the capsules daily for 7 consecutive days. On the testing day, the capsules are ingested 60 minutes prior to the exercise tests.

Placebo

Eligibility Criteria

Age20 Years - 30 Years
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Absence of neuromuscular and musculoskeletal disorders
  • At least 2 years of regular resistance training experience (minimum 3 sessions per week)
  • At least 6 months of resistance training prior to enrollment
  • Absence of renal and hepatic disorders
  • Daily caffeine consumption of 5 mg/kg body weight (based on questionnaire)
  • No use of specific medications or supplements that could affect study outcomes (e.g., beta-alanine, creatine, pre-workout supplements) -

You may not qualify if:

  • Occurrence of any injury during the study
  • Failure to adhere to the supplement consumption protocol
  • Withdrawal from the study-

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Faculty of Sport Sciences, University of Birjand

Birjand, South Khorasan Province, 9717434765, Iran

Location

MeSH Terms

Interventions

Caffeine

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
Double Blind
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor of Exercise Physiology

Study Record Dates

First Submitted

September 15, 2026

First Posted

September 21, 2026

Study Start

February 12, 2023

Primary Completion

March 20, 2023

Study Completion

March 30, 2023

Last Updated

September 21, 2026

Record last verified: 2026-09

Data Sharing

IPD Sharing
Will not share

Locations