- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07240506
Effect of Caffeinated Chewing Gum on Vertical Jump Performance in Female Volleyball Players (CAF-GUM)
Effect of Acute Caffeine Intake Via Caffeinated Gum on Vertical Jump Performance in Female Volleyball Players: A Single-Blind Placebo-Controlled Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Caffeine is a well-established ergogenic aid known to improve endurance, strength, and cognitive performance. However, limited evidence exists on its acute effects in female team-sport athletes. This study was designed to evaluate the impact of acute caffeine intake via caffeinated chewing gum on vertical jump performance among professional female volleyball players. The research employed a randomized, single-blind, placebo-controlled crossover design.
Ten professional athletes aged 18-33 years from the Yeşilyurt Sports Club Women's A Team, competing in the Turkish Volleyball Federation Women's 1st League, were included. Participants underwent two experimental sessions: one involving caffeinated gum (CAF, 200 mg total caffeine from two 100 mg pieces) and one involving placebo gum (PLA, identical but caffeine-free), separated by a six-day washout period. The gums were chewed for 5 minutes, and jump performance tests were conducted 15 minutes later.
Vertical jump performance was evaluated using a Chronojump jump mat for three jump types: squat jump (SJ), countermovement jump (CMJ), and block jump (BJ). Each test included three attempts, with the highest score recorded for analysis. Data were analyzed with paired-sample t-tests using SPSS 27.0, with significance set at p<0.05.
The results showed that caffeine gum significantly increased CMJ height compared with the placebo (p<0.05), but no significant effects were observed for SJ or BJ performance. The findings indicate that caffeine in gum form may acutely improve explosive performance involving stretch-shortening cycle movements.
The study was approved by the Non-Interventional Clinical Research Ethics Committee of Istanbul Medipol University (Approval No: E-10840098-202.3.02-735). All participants provided informed consent prior to data collection.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Bakırköy
-
Istanbul, Bakırköy, Turkey (Türkiye), 34149
- Yeşilyurt Sports Club - Women's Volleyball Team Training Facility
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
Self-identified female athletes aged 18-33 years Professional volleyball players actively competing in the Turkish Women's Volleyball First League Minimum of 3 years of competitive volleyball experience Healthy individuals without any diagnosed medical conditions Willing to abstain from caffeine-containing products for at least 24 hours before each testing session Voluntarily agreed to participate and provided written informed consent
Exclusion Criteria:
Known cardiovascular, metabolic, or neurological disorders Current use of medications or supplements affecting physical performance or caffeine metabolism Pregnancy or breastfeeding History of caffeine sensitivity, intolerance, or allergy Failure to comply with pre-test instructions (e.g., caffeine restriction, rest period) Musculoskeletal injuries preventing full jump performance
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Caffeinated Gum (CAF)
Participants chewed two pieces of caffeinated chewing gum containing a total of 200 mg caffeine (2 × 100 mg).
After chewing for 5 minutes, they performed squat jump, countermovement jump, and block jump tests.
|
Two pieces of caffeinated chewing gum providing 200 mg total caffeine; administered 15 minutes before performance testing.
|
|
Placebo Comparator: Placebo Gum (PLA)
Participants chewed two pieces of placebo chewing gum identical in appearance and flavor but containing no caffeine.
After chewing for 5 minutes, they performed the same vertical jump tests as in the caffeinated condition.
|
Two pieces of placebo chewing gum identical in appearance and flavor to the caffeinated gum but containing no caffeine; administered 15 minutes before performance testing.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Countermovement Jump Height
Time Frame: Within 15 minutes after gum administration.
|
Change in countermovement jump (CMJ) height measured using a Chronojump contact mat following caffeine or placebo gum ingestion.
|
Within 15 minutes after gum administration.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Squat Jump Height
Time Frame: Within 15 minutes after gum administration.
|
Change in squat jump (SJ) height measured using a Chronojump contact mat after caffeine or placebo gum ingestion.
|
Within 15 minutes after gum administration.
|
|
Block Jump Height
Time Frame: Within 15 minutes after gum administration.
|
Change in block jump (BJ) height measured using a Chronojump contact mat after caffeine or placebo gum ingestion.
|
Within 15 minutes after gum administration.
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- E-10840098-202.3.02-735
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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