- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07056231
- Original Trial
Effect of Low-Dose Caffeine on Performance in Elite Sitting Volleyball Players
June 28, 2025 updated by: Ulaç Can YILDIRIM
The Effect of Low Dose Caffeine on Serve Speed, Spike Speed, and Speed-Endurance in Elite Sitting Volleyball Players: A Randomized Double-Blind Crossover Study
Background: Sitting volleyball is a sport that relies primarily on upper body strength and anaerobic capacity.
In critical in-game skills such as serve and spike, factors such as speed-endurance time and impact power play a decisive role in performance.
There are limited studies in the literature examining the effects of low-dose caffeine consumption on these skills.
The effects of ergogenic supplements in Paralympic sports have not been sufficiently investigated, and the potential benefits of caffeine on serve and spike performance in sitting volleyball players remain unclear.
Purpose: The main purpose of this research was to determine the effects of low-dose caffeine (3 mg/kg) consumption on the serve speed, spike speed and Speed-Endurance performances of elite-level sitting volleyball players.
Method: The study was designed using a randomized, double-blind, balanced, and crossover experimental design.
13 elite male athletes from the 2024 Paravolley European Champion Sitting Volleyball Men's National Team participated in the study.
Participants were evaluated for serve speed, spike speed, and speed-endurance performances in both 3 mg/kg caffeine (CAF) and placebo (PLA) conditions.
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
This study aimed to investigate the effects of low-dose caffeine ingestion on key performance parameters in elite-level sitting volleyball athletes.
Sitting volleyball is a Paralympic sport that relies heavily on upper body explosive strength and short-term anaerobic power.
While caffeine is a well-known ergogenic aid in able-bodied sports, its role in Paralympic contexts remains underexplored.
Using a randomized, double-blind, placebo-controlled crossover design, the effects of 3 mg/kg caffeine consumption were assessed in 13 elite male sitting volleyball players.
Each participant completed performance assessments under both caffeine and placebo conditions.
The primary goal was to examine whether caffeine intake would enhance serve speed, spike speed, and repeated sprint ability.
The study provides new insights into the acute ergogenic effects of caffeine in Paralympic team sport athletes, highlighting its selective benefit on explosive upper-body tasks such as serving.
Study Type
Interventional
Enrollment (Actual)
13
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Central
-
Karaman, Central, Turkey, 695002
- Karamanoğlu Mehmetbey University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Male sitting volleyball players aged between 18 and 40
- Member of the 2024 National Sitting Volleyball Team
- At least 3 years of competitive playing experience
- No caffeine consumption 48 hours prior to testing
- Provided informed consent to participate
Exclusion Criteria:
- Known cardiovascular, neurological, or metabolic disorders
- Current use of medications that may affect caffeine metabolism
- Allergy or sensitivity to caffeine
- Use of performance-enhancing substances within the last month
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Quadruple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Low-Dose Caffeine Arm
Participants receive a single oral dose of caffeine (3 mg/kg) during the first session and a placebo in the second session.
There is a washout period of at least 48 hours between sessions.
|
A single oral dose of 3 mg of caffeine per kilogram of body weight form approximately 60 minutes before performance testing.
Supplied by Oxford Vitality, ISO-certified.
polydextrose used as Placebo
|
|
Experimental: Placebo Arm
Participants receive a placebo during the first session and a single oral dose of caffeine (3 mg/kg) in the second session.
There is a washout period of at least 48 hours between sessions.
|
A single oral dose of 3 mg of caffeine per kilogram of body weight form approximately 60 minutes before performance testing.
Supplied by Oxford Vitality, ISO-certified.
polydextrose used as Placebo
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Serve Speed
Time Frame: After 60 minutes ingestion of the supplement on test day (CAF and PLA)
|
Serve speed will be assessed using a calibrated radar device to record peak velocity of each participant's volleyball serve.
|
After 60 minutes ingestion of the supplement on test day (CAF and PLA)
|
|
Spike Speed
Time Frame: After 60 minutes ingestion of the supplement on test day (CAF and PLA)
|
Maximum spike speed will be measured in kilometers per hour (km/h) using a radar gun during a standardized spike task conducted after supplementation in each condition.
|
After 60 minutes ingestion of the supplement on test day (CAF and PLA)
|
|
Speed-Endurance
Time Frame: After 60 minutes ingestion of the supplement on test day (CAF and PLA)
|
The number of maximal shuttle runs completed in a repeated sprint ability (RSA) test protocol will be recorded to assess speed-endurance capacity.
|
After 60 minutes ingestion of the supplement on test day (CAF and PLA)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Ulas C Yildirim, sinop university faculty of sport sciences
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 5, 2025
Primary Completion (Actual)
March 11, 2025
Study Completion (Actual)
March 12, 2025
Study Registration Dates
First Submitted
June 21, 2025
First Submitted That Met QC Criteria
June 28, 2025
First Posted (Actual)
July 9, 2025
Study Record Updates
Last Update Posted (Actual)
July 9, 2025
Last Update Submitted That Met QC Criteria
June 28, 2025
Last Verified
June 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2025/91
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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