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CompletedNCT07889661CAFF-WRESTUpdated Oct 22, 2026

Caffeine and Wrestling Performance in Male Wrestlers of Different Weight Classes: A Randomized Crossover Trial

An interventional study of Caffeine in Athletic Performance, Caffeine and Wrestling, sponsored by Islamic Azad University, Abadan Branch. Completed at 1 site in Iran. Open to male participants aged 15 Years to 40 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-22.

Sponsored by Islamic Azad University, Abadan Branch · Not applicable, Interventional, and Other

From the registry’s dates

  • Registered 6 months after the study started (first participant enrolled Mar 2026, registered Oct 2026).
Updated Oct 22, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
95
Allocation
Randomized
Ages
15 Years to 40 Years
Sex
Male
01

Study summary

Caffeine is commonly used by athletes to improve performance, but not everyone responds to it in the same way. In weight-class sports like wrestling, athletes are grouped by body weight. When caffeine is dosed based on body weight (4 mg per kg), heavier athletes receive a larger total amount of caffeine than lighter athletes. This study asked whether the effects of caffeine on wrestling performance and side effects differ across wrestling weight classes.

Ninety-five male wrestlers (30 lightweight, 36 middleweight, and 29 heavyweight) completed two testing sessions: one after taking caffeine (4 mg/kg) and one after taking a placebo (an inactive capsule). Neither the wrestlers nor the researchers knew which capsule was given in each session. Each session included a countermovement jump test and a wrestling-specific fitness test that involved throwing a wrestling dummy. Heart rate, perceived exertion, and self-reported symptoms were also recorded.

The study found that lightweight and middleweight wrestlers generally performed better after caffeine, while heavyweight wrestlers showed no performance improvement and reported more side effects, such as anxiety, rapid heartbeat, stomach discomfort, and insomnia. These differences occurred even though all wrestlers received the same caffeine dose relative to their body weight.

The results suggest that a standard body-weight-based caffeine dose may not work equally well for all wrestlers. Lighter wrestlers may benefit more, while heavier wrestlers may experience more side effects without performance gains. These findings support the need for individualized caffeine dosing strategies in wrestling and similar weight-class sports. However, because body weight, total caffeine dose, and other weight-class-related factors were not separated in this study, the results should be considered exploratory and do not establish weight-specific recommendations.

02

Conditions studied

  • Athletic Performance
  • Caffeine
  • Wrestling
03

In context

Lead sponsor

This is the only study on the registry with Islamic Azad University, Abadan Branch as lead sponsor.

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

04

Who can participate

Ages eligible
15 Years to 40 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Male wrestlers aged 15 to 35 years.
  • Competing in Greco-Roman or freestyle wrestling.
  • At least four years of systematic wrestling training experience (for the parent trial) or at least three years of continuous wrestling training (for the secondary analysis).
  • Competing consistently in a fixed Olympic weight category for at least the previous two years.
  • Maintaining current body weight within 3 kg of competition weight.
  • No competition or tournament participation within the last month before the study.
  • Regular participation in organized training (at least 3 sessions per week).
  • Current involvement in freestyle or Greco-Roman wrestling at amateur, semi-professional, or professional level.
  • Willing to provide written informed consent.
  • Willing to abstain from caffeine-containing foods, beverages, and supplements for 24 hours before each testing session.
  • Willing to avoid strenuous exercise for 24 hours before each testing session.

Exclusion criteria

Exclusion Criteria:

  • History of cardiovascular, metabolic, or neurological disorders.
  • History of respiratory or gastrointestinal disease.
  • Regular use of medication that could interfere with study outcomes.
  • Current smoking or substance abuse.
  • Injury or illness within the two weeks before the study.
  • Injury limiting maximal exercise performance.
  • Rapid weight reduction within the month before the study.
  • Unwillingness to comply with study procedures or follow-up.
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Triple (Participant, Investigator, Outcomes assessor)
Enrollment
95 participants (actual)

Study arms

  • Experimental
    Caffeine then Placebo

    Participants in this arm received a caffeine capsule (4 mg/kg body mass) in the first experimental session and a placebo capsule (dextrose) in the second experimental session, with a 1-week washout period between sessions. Capsules were administered 60 minutes before performance testing. Participants completed countermovement jump testing and the Special Wrestling Fitness Test (SWFT) in each session.

    Drug: Caffeine

  • Experimental
    Placebo then Caffeine

    Participants in this arm received a placebo capsule (dextrose) in the first experimental session and a caffeine capsule (4 mg/kg body mass) in the second experimental session, with a 1-week washout period between sessions. Capsules were administered 60 minutes before performance testing. Participants completed countermovement jump testing and the Special Wrestling Fitness Test (SWFT) in each session.

    Drug: Caffeine

Interventions

  • Anhydrous caffeine powder (Sigma-Aldrich, Steinheim, Germany) encapsulated in identical opaque gelatin capsules. Administered orally at a dose of 4 mg/kg body mass with approximately 200 mL of water, 60 minutes before performance testing.

06

What researchers measure

Primary outcomes

  1. Total number of throws (Tn)

    Total number of successful throws completed across the three active periods of the Special Wrestling Fitness Test (SWFT). A throw was considered correct only when it satisfied the technical scoring criteria of United World Wrestling. Three independent assessors counted the throws, with discrepancies resolved through discussion.

    Time frame: Measured during each experimental session, 60 minutes after supplementation.

  2. Performance Index (PI)

    A wrestling-specific performance index calculated as (HR0 + HR1) / Tn, where HR0 is heart rate immediately after the SWFT and HR1 is heart rate 1 minute after the SWFT. A lower performance-index value indicates a greater number of throws relative to the recorded cardiac response.

    Time frame: Measured during each experimental session, 60 minutes after supplementation.

Secondary outcomes

  1. Body-mass-normalized throws (TnW)

    Total number of throws normalized to body weight, calculated as Tn divided by body weight in kilograms (TnW = Tn / body weight). This outcome reflects wrestling-specific work relative to body weight and has shown strong predictive validity for wrestling performance.

    Time frame: Measured during each experimental session, 60 minutes after supplementation.

  2. Countermovement jump performance

    Lower-body explosive power assessed using the Sargent vertical jump test (wall-mounted reach method). Participants performed three maximal countermovement jumps with 60 s passive recovery between attempts. Jump height (cm) was calculated as the difference between standing reach and maximal jump reach. The highest value was retained for analysis.

    Time frame: 60 minutes after supplementation, before the Special Wrestling Fitness Test (SWFT).

  3. Rating of perceived exertion (RPE)

    Overall perceived exertion during the SWFT, assessed using the 10-point Borg scale immediately after the test.

    Time frame: Immediately after the SWFT.

  4. Self-reported symptoms on the test day

    Presence or absence of negative symptoms assessed using an adapted QUEST checklist: anxiety, headache, dizziness, nervousness, irritability, tachycardia, abdominal discomfort, increased urine output, muscle soreness, and fatigue. Each item recorded dichotomously (yes/no). Vigor/activeness was treated separately as a positive self-reported effect and excluded from the adverse-symptom composite.

    Time frame: Immediately after each testing session (test day).

  5. Self-reported symptoms on the following day

    Presence or absence of negative symptoms including insomnia, assessed 24 hours after each testing session using the same adapted QUEST checklist.

    Time frame: 24 hours after each testing session.

07

Study locations

1 site
  • Islamic Azad University, Arvand Branch, Abadan
    Ābādān, Khuzestan, Iran
08

References and documents

Study documents

  • Study protocol · Mar 3, 2026
  • Informed consent form · Feb 1, 2026

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: Yes

Supporting information: Study protocol, Statistical analysis plan, Informed consent form, Analytic code

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 22, 2026
Show all 1 update
  1. Oct 22, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07889661
Lead sponsor
Islamic Azad University, Abadan Branch
Responsible party
Raoof Negaresh (Assistant Professor and Principal Investigator, Islamic Azad University, Arvand Branch, Science & Research Islamic Azad University Branch Khozestan) — Principal investigator
First posted
Oct 22, 2026
Start date
Mar 30, 2026
Primary completion
Jun 4, 2026
Completion
Jun 6, 2026
Last update
Oct 22, 2026

Study contacts

Raoof Negaresh, PhD
principal investigator · Farhangian University

Oversight

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

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Studies of the drug tested here: Caffeine

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