Caffeinated Gum Use and Volleyball Performance
15 мая 2026 г. обновлено: Gülbin Rudarlı, Ege University
Acute Effects of Caffeinated Gum Use on Volleyball Performance: A Randomized, Placebo-Controlled Crossover Trial
This study examined the acute effects of caffeinated chewing gum on volleyball performance in trained female volleyball players. Caffeine is commonly used by athletes to improve performance, but less is known about whether caffeinated gum is useful during volleyball-specific activity.
Participants completed three testing sessions in a randomized crossover design. In one session, they chewed placebo gum. In another session, they chewed caffeinated gum containing a single 300 mg dose of caffeine. In the third session, they received the same total amount of caffeine as three separate 100 mg doses given at 30-minute intervals.
The study assessed volleyball-specific skill performance, including attack, block, and defense efficiency, during a volleyball-specific skill game. Vertical jump height, heart rate, perceived exertion, side effects, and condition guessing were also recorded.
Обзор исследования
Статус
Завершенный
Условия
Подробное описание
This randomized, placebo-controlled, crossover study investigated whether the pattern of caffeinated gum administration affects volleyball-specific performance in trained female volleyball players. Participants completed one familiarization session and three experimental sessions separated by one week. The experimental conditions were placebo gum, single-dose caffeinated gum, and partial-dose caffeinated gum.
In the single-dose condition, participants chewed three pieces of caffeinated gum containing a total of 300 mg caffeine for 5 minutes. In the partial-dose condition, participants chewed one piece of caffeinated gum containing 100 mg caffeine at three different time points, with 30-minute intervals between doses. In the placebo condition, participants chewed caffeine-free gum for 5 minutes.
Each testing session included volleyball-specific activities and a 30-minute volleyball-specific skill game. Attack, block, and defense efficiency were assessed using video recordings and Data Volley software. Vertical jump height was measured before and after the volleyball-specific activity. Heart rate was recorded during the session, and rating of perceived exertion was assessed before and after the session. Participants were also asked to report side effects and to guess which condition they had received after each session.
Тип исследования
Интервенционный
Регистрация (Действительный)
11
Фаза
- Непригодный
Контакты и местонахождение
В этом разделе приведены контактные данные лиц, проводящих исследование, и информация о том, где проводится это исследование.
Места учебы
-
-
Bornova
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Izmir, Bornova, Турция (Туркие), 35040
- Ege University, Faculty of Sport Sciences
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Критерии участия
Исследователи ищут людей, которые соответствуют определенному описанию, называемому критериям приемлемости. Некоторыми примерами этих критериев являются общее состояние здоровья человека или предшествующее лечение.
Критерии приемлемости
Возраст, подходящий для обучения
- Взрослый
Принимает здоровых добровольцев
Да
Описание
Inclusion Criteria:
- Female volleyball players aged 18 to 35 years.
- Apparently healthy.
- Daily caffeine intake ≤300 mg.
- Minimum of 5 years of regular volleyball training experience.
- Training for at least 120 minutes at least 3 days per week.
- Competing in national or international volleyball matches.
- Provided written informed consent before participation.
Exclusion Criteria:
- Serious injury or trauma within the past 6 months that could affect volleyball performance.
- Illness or inability to continue the study protocol during the research period.
- Development of side effects during caffeinated gum administration that prevented continuation.
- Regular alcohol or drug use that could affect the study outcomes.
Учебный план
В этом разделе представлена подробная информация о плане исследования, в том числе о том, как планируется исследование и что оно измеряет.
Как устроено исследование?
Детали дизайна
- Основная цель: Другой
- Распределение: Рандомизированный
- Интервенционная модель: Назначение кроссовера
- Маскировка: Двойной
Оружие и интервенции
Группа участников / Армия |
Вмешательство/лечение |
|---|---|
|
Экспериментальный: Placebo, Single-Dose Caffeine, Partial-Dose Caffeine Arm Type: Experimental
Participants received placebo gum in the first session, single-dose caffeinated gum in the second session, and partial-dose caffeinated gum in the third session.
Sessions were separated by one week.
|
Participants chewed three pieces of caffeinated gum containing 100 mg caffeine per piece, providing a total dose of 300 mg caffeine.
The gum was chewed for 5 minutes and then discarded.
Другие имена:
Participants received three separate pieces of caffeinated gum containing 100 mg caffeine per piece.
One piece was chewed for 5 minutes at each administration time point, with doses given at 30-minute intervals, providing a total dose of 300 mg caffeine.
Другие имена:
Participants chewed caffeine-free placebo gum for 5 minutes.
The placebo gum was selected to be similar in shape and color to the caffeinated gum.
Другие имена:
|
|
Экспериментальный: Placebo, Partial-Dose Caffeine, Single-Dose Caffeine
Participants received placebo gum in the first session, partial-dose caffeinated gum in the second session, and single-dose caffeinated gum in the third session.
Sessions were separated by one week.
|
Participants chewed three pieces of caffeinated gum containing 100 mg caffeine per piece, providing a total dose of 300 mg caffeine.
The gum was chewed for 5 minutes and then discarded.
Другие имена:
Participants received three separate pieces of caffeinated gum containing 100 mg caffeine per piece.
One piece was chewed for 5 minutes at each administration time point, with doses given at 30-minute intervals, providing a total dose of 300 mg caffeine.
Другие имена:
Participants chewed caffeine-free placebo gum for 5 minutes.
The placebo gum was selected to be similar in shape and color to the caffeinated gum.
Другие имена:
|
|
Экспериментальный: Single-Dose Caffeine, Placebo, Partial-Dose Caffeine
Participants received single-dose caffeinated gum in the first session, placebo gum in the second session, and partial-dose caffeinated gum in the third session.
Sessions were separated by one week.
|
Participants chewed three pieces of caffeinated gum containing 100 mg caffeine per piece, providing a total dose of 300 mg caffeine.
The gum was chewed for 5 minutes and then discarded.
Другие имена:
Participants received three separate pieces of caffeinated gum containing 100 mg caffeine per piece.
One piece was chewed for 5 minutes at each administration time point, with doses given at 30-minute intervals, providing a total dose of 300 mg caffeine.
Другие имена:
Participants chewed caffeine-free placebo gum for 5 minutes.
The placebo gum was selected to be similar in shape and color to the caffeinated gum.
Другие имена:
|
|
Экспериментальный: Single-Dose Caffeine, Partial-Dose Caffeine, Placebo
Participants received single-dose caffeinated gum in the first session, partial-dose caffeinated gum in the second session, and placebo gum in the third session.
Sessions were separated by one week.
|
Participants chewed three pieces of caffeinated gum containing 100 mg caffeine per piece, providing a total dose of 300 mg caffeine.
The gum was chewed for 5 minutes and then discarded.
Другие имена:
Participants received three separate pieces of caffeinated gum containing 100 mg caffeine per piece.
One piece was chewed for 5 minutes at each administration time point, with doses given at 30-minute intervals, providing a total dose of 300 mg caffeine.
Другие имена:
Participants chewed caffeine-free placebo gum for 5 minutes.
The placebo gum was selected to be similar in shape and color to the caffeinated gum.
Другие имена:
|
|
Экспериментальный: Partial-Dose Caffeine, Placebo, Single-Dose Caffeine
Participants received partial-dose caffeinated gum in the first session, placebo gum in the second session, and single-dose caffeinated gum in the third session.
Sessions were separated by one week.
|
Participants chewed three pieces of caffeinated gum containing 100 mg caffeine per piece, providing a total dose of 300 mg caffeine.
The gum was chewed for 5 minutes and then discarded.
Другие имена:
Participants received three separate pieces of caffeinated gum containing 100 mg caffeine per piece.
One piece was chewed for 5 minutes at each administration time point, with doses given at 30-minute intervals, providing a total dose of 300 mg caffeine.
Другие имена:
Participants chewed caffeine-free placebo gum for 5 minutes.
The placebo gum was selected to be similar in shape and color to the caffeinated gum.
Другие имена:
|
|
Экспериментальный: Partial-Dose Caffeine, Single-Dose Caffeine, Placebo
Participants received partial-dose caffeinated gum in the first session, single-dose caffeinated gum in the second session, and placebo gum in the third session.
Sessions were separated by one week.
|
Participants chewed three pieces of caffeinated gum containing 100 mg caffeine per piece, providing a total dose of 300 mg caffeine.
The gum was chewed for 5 minutes and then discarded.
Другие имена:
Participants received three separate pieces of caffeinated gum containing 100 mg caffeine per piece.
One piece was chewed for 5 minutes at each administration time point, with doses given at 30-minute intervals, providing a total dose of 300 mg caffeine.
Другие имена:
Participants chewed caffeine-free placebo gum for 5 minutes.
The placebo gum was selected to be similar in shape and color to the caffeinated gum.
Другие имена:
|
Что измеряет исследование?
Первичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
Attack efficiency
Временное ограничение: During the 30-minute volleyball-specific skill game in each experimental trial
|
Attack efficiency was assessed during a 30-minute volleyball-specific skill game using video recordings and Data Volley software.
Values were expressed as percentages.
|
During the 30-minute volleyball-specific skill game in each experimental trial
|
|
Block efficiency
Временное ограничение: During the 30-minute volleyball-specific skill game in each experimental trial
|
Block efficiency was assessed during a 30-minute volleyball-specific skill game using video recordings and Data Volley software.
Values were expressed as percentages.
|
During the 30-minute volleyball-specific skill game in each experimental trial
|
|
Defense efficiency
Временное ограничение: During the 30-minute volleyball-specific skill game in each experimental trial
|
Defense efficiency was assessed during a 30-minute volleyball-specific skill game using video recordings and Data Volley software.
Values were expressed as percentages.
|
During the 30-minute volleyball-specific skill game in each experimental trial
|
Вторичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
Change in vertical jump height
Временное ограничение: From immediately before to immediately after each experimental trial
|
Vertical jump height was measured before and after each experimental testing session using a photoelectric cell system.
Values were expressed in centimeters.
|
From immediately before to immediately after each experimental trial
|
|
Heart rate
Временное ограничение: Continuously during each experimental trial
|
Heart rate was recorded during each experimental testing session using a telemetric heart rate monitoring system.
Values were expressed as beats per minute.
|
Continuously during each experimental trial
|
|
Change in rating of perceived exertion
Временное ограничение: From immediately before to immediately after each experimental trial
|
Rating of perceived exertion was assessed before and after each experimental testing session using a 0-10 Borg scale.
|
From immediately before to immediately after each experimental trial
|
Другие показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
Side effects
Временное ограничение: Immediately after each experimental trial
|
Participants were asked after each experimental testing session whether they experienced any side effects or discomfort related to the gum intervention.
Reported responses were recorded descriptively.
|
Immediately after each experimental trial
|
Соавторы и исследователи
Здесь вы найдете людей и организации, участвующие в этом исследовании.
Спонсор
Даты записи исследования
Эти даты отслеживают ход отправки отчетов об исследованиях и сводных результатов на сайт ClinicalTrials.gov. Записи исследований и сообщаемые результаты проверяются Национальной медицинской библиотекой (NLM), чтобы убедиться, что они соответствуют определенным стандартам контроля качества, прежде чем публиковать их на общедоступном веб-сайте.
Изучение основных дат
Начало исследования (Действительный)
5 августа 2025 г.
Первичное завершение (Действительный)
23 апреля 2026 г.
Завершение исследования (Действительный)
23 апреля 2026 г.
Даты регистрации исследования
Первый отправленный
11 мая 2026 г.
Впервые представлено, что соответствует критериям контроля качества
15 мая 2026 г.
Первый опубликованный (Действительный)
19 мая 2026 г.
Обновления учебных записей
Последнее опубликованное обновление (Действительный)
19 мая 2026 г.
Последнее отправленное обновление, отвечающее критериям контроля качества
15 мая 2026 г.
Последняя проверка
1 мая 2026 г.
Дополнительная информация
Термины, связанные с этим исследованием
Ключевые слова
Другие идентификационные номера исследования
- EGE-25-9.1T-28
Планирование данных отдельных участников (IPD)
Планируете делиться данными об отдельных участниках (IPD)?
НЕТ
Описание плана IPD
Individual participant data will not be shared because the dataset contains participant-level performance and physiological data from a small group of elite female volleyball players, which may increase the risk of participant identification.
Информация о лекарствах и устройствах, исследовательские документы
Изучает лекарственный продукт, регулируемый FDA США.
Нет
Изучает продукт устройства, регулируемый Управлением по санитарному надзору за качеством пищевых продуктов и медикаментов США.
Нет
Эта информация была получена непосредственно с веб-сайта clinicaltrials.gov без каких-либо изменений. Если у вас есть запросы на изменение, удаление или обновление сведений об исследовании, обращайтесь по адресу register@clinicaltrials.gov. Как только изменение будет реализовано на clinicaltrials.gov, оно будет автоматически обновлено и на нашем веб-сайте. .