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Combined Caffeine and Rhodiola Rosea on Aerial Duel Performance in Soccer

Effects of Combined Caffeine and Rhodiola Rosea Supplementation on Aerial Duel Performance Under Fatigue in Soccer Players

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07458594
Acronym
CCRP-AD
Enrollment
96
Registered
2026-03-09
Start date
2025-10-30
Completion date
2026-01-03
Last updated
2026-03-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aerial Duel Performance in Soccer Players

Keywords

Caffeine, Rhodiola rosea, Combined Supplementation, Soccer Performance, Neuromuscular Fatigue, Countermovement Jump (CMJ), Early Impulse (Impulse₀-₂₀₀), Aerial Duel

Brief summary

This study will examine whether caffeine (CAF) and Rhodiola rosea (RHO) supplementation, taken alone or in combination, can improve explosive performance and soccer-specific aerial duel performance in trained male soccer players. In a randomized, double-blind, placebo-controlled, parallel design, participants will be assigned to placebo, RHO, CAF, or RHO+CAF for 4 weeks. Performance outcomes will be assessed before and after the intervention using countermovement jump measures (including early take-off impulse) and standardized heading tests (heading reach height, ball exit velocity, and heading duel success rate), with additional measures of neck isometric strength and perceived exertion.

Interventions

DIETARY_SUPPLEMENTCaffeine

Anhydrous caffeine capsules administered at a dose of 3 mg/kg body weight. Taken as a single dose 30 minutes prior to the physical performance tests.

DIETARY_SUPPLEMENTRhodiola rosea extract

Standardized Rhodiola rosea extract capsules. Daily total dosage of 2.4 g (containing approx. 12 mg salidroside), taken twice daily (before breakfast and lunch) for 30 days.

DIETARY_SUPPLEMENTPlacebo

Appearance-matched capsules containing inert ingredients (starch or rice flour).

Sponsors

Beijing Sport University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Masking description

Participants, outcome assessors, and data analysts are blinded to group allocation. Supplement distribution and group coding are managed by an independent researcher not involved in data collection or statistical analysis. All capsules are identical in appearance to maintain blinding throughout the study period.

Intervention model description

This is a 4-week, randomized, double-blind, placebo-controlled, parallel-group trial with four arms (placebo, Rhodiola rosea, caffeine, and Rhodiola rosea plus caffeine; n=24 per arm). Participants complete identical pre- and post-intervention testing sessions. Rhodiola rosea is administered daily throughout the intervention period, while caffeine is administered acutely prior to the test sessions; matching placebo capsules are used to maintain blinding across all groups.

Eligibility

Sex/Gender
MALE
Age
18 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy male soccer players from the Beijing Sport University team. Systematic soccer-specific training background and stable competitive level. Suitable for high-intensity physical testing based on the Physical Activity Readiness Questionnaire (PAR-Q).

Exclusion criteria

* History of neuromuscular or musculoskeletal system diseases. Intake of caffeine (coffee/tea), other supplements, ergogenic aids, or alcohol within the last 3 months. Current use of antidepressants or central nervous system stimulants. Smokers.

Design outcomes

Primary

MeasureTime frameDescription
Early takeoff impulse (Impulse₀-₂₀₀)Baseline (Day 0) and Post-intervention (Day 30), measured under both non-fatigued and fatigued conditions.Calculated as the integration of vertical force over the first 200 ms of the countermovement jump (CMJ) takeoff phase, relative to body mass (N·s·kg-¹). This measures the capacity for rapid force production.

Secondary

MeasureTime frameDescription
Heading contact heightBaseline (Pre-test) and 4 weeks (Post-test), including measurements under both non-fatigued and fatigued conditions at each time point.Participants perform a header and touch a football suspended on a vertical jump tester with their forehead. The highest touch height from three trials is recorded to reflect aerial reach capacity.
Heading Ball VelocityBaseline (Pre-test) and 4 weeks (Post-test), including measurements under both non-fatigued and fatigued conditions at each time point.The maximum velocity of the ball after heading is measured using a speed device. A ball machine is used to ensure consistent delivery direction and speed. This measures momentum transfer efficiency and technical execution.
Aerial Duel Success RateBaseline (Pre-test) and 4 weeks (Post-test), including measurements under both non-fatigued and fatigued conditions at each time point.Calculated as the percentage of successful duels out of a fixed number of trials in a standardized head-to-head setting. Success is defined as effectively contacting the ball first and directing it toward a target area.
Neck Isometric StrengthBaseline (Pre-test) and 4 weeks (Post-test).Maximum isometric force measured in neck flexion and extension using a handheld dynamometer. Values are normalized to body mass ($N \\cdot kg\^{-1}$) to assess the stability of the head-trunk system.
Rate of Perceived Exertion (RPE)Immediately after the fatigue-induction protocol and post-fatigue testing at Baseline and 4 weeks.Subjective effort level reported by participants on a scale of 1 to 10 (1 = nearly no effort, 10 = extreme effort) immediately following the fatigue protocol and post-fatigue tests.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 10, 2026