An Initial Investigation Into the Effects of β-Alanine on Performance and Physiological Responses During Simulated Wrestling Matches
8 de junho de 2026 atualizado por: China Medical University Hospital
This research aims to investigate the effects of beta-alanine (BA) supplementation on simulated 2-day freestyle wrestling performance, as well as on exercise-induced muscle fatigue and oxidative stress in wrestlers.
In addition to the common issue of long-term insufficient energy intake due to weight control, high-intensity training can further exacerbate exercise-induced oxidative stress and muscle fatigue, thereby impairing athletic performance.
Therefore, finding effective ergogenic aids to reduce these negative physiological responses is crucial for optimizing athletes' competitive condition.
Based on a literature review, this study will implement the Specific Wrestling Performance Test (SWPT) to simulate two consecutive days of freestyle wrestling competitions according to Kraemer's model.
Multiple performance assessments will be used to evaluate the impact of BA supplementation on athletes' physiological indicators and performance.
It is expected that BA supplementation will enhance systemic antioxidant capacity, reduce muscle fatigue and oxidative stress induced by simulated wrestling matches, and improve wrestling-specific physical performance.
Visão geral do estudo
Status
Ativo, não recrutando
Intervenção / Tratamento
Descrição detalhada
This experiment will employ the Specific Wrestling Performance Test (SWPT) to conduct the two-day simulated freestyle wrestling competition protocol developed by Kraemer (Kraemer et al., 2001), in order to evaluate the physiological responses of athletes during competition.
A total of 20 wrestlers will participate in this study using a randomized single-blind crossover design.
Participants will receive either beta-alanine (BA) supplementation or a placebo for four weeks (4.8 g/day), followed by a four-week washout period.
On the official testing day, body composition measurements and records will be taken 12 hours before the first SWPT session.
After the measurements, participants will be provided with a 300 kcal light meal.
Following the completion of the third SWPT session, participants will perform approximately 20-30 minutes of cycling exercise to help maintain body weight for the following morning.
Two hours before the fourth SWPT session, body weight will be measured again to ensure that weight variation does not exceed 2%, after which another 300 kcal light meal will be provided.
The simulated two-day freestyle wrestling competition protocol will consist of five SWPT sessions: on Day 1, SWPT sessions will be conducted at 10:00 AM, 2:00 PM, and 6:00 PM; on Day 2, sessions will take place at 10:00 AM and 7:00 PM.
In this crossover trial, all pre-competition assessments will be conducted before the matches.
Pre-test assessments must be completed 10 minutes before the start of the first SWPT session, while post-test assessments will be conducted immediately after each SWPT session.
The assessment items include the number of throws completed during the simulated SWPT match, reaction tests, grip strength tests, back strength tests, and sport-specific fitness tests.
In addition, ratings of perceived exertion (RPE), heart rate, and blood samples will be recorded and collected.
The sport-specific fitness tests include the Overhead Medicine Ball Throw (OMBT) and the Medicine Ball Chest Throw (MBCT).
Tipo de estudo
Intervencional
Inscrição (Real)
16
Estágio
- Não aplicável
Contactos e Locais
Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.
Locais de estudo
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Taichung, Taiwan
- China Medical University
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Critérios de participação
Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.
Critérios de elegibilidade
Idades elegíveis para estudo
- Filho
- Adulto
Aceita Voluntários Saudáveis
Sim
Descrição
Inclusion Criteria:
- Wrestle athletes aged 12 to 25 years with at least 3 years of wrestle training experience.
Exclusion Criteria:
- All participants must be free from chronic conditions such as heart disease and hypertension, and must not have experienced any serious lower limb musculoskeletal injuries within the past six months.
Plano de estudo
Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Outro
- Alocação: Randomizado
- Modelo Intervencional: Atribuição cruzada
- Mascaramento: Quadruplicar
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
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Comparador de Placebo: Placebo
Contendo amarelo comestível nº 4, amarelo comestível nº 5, sacarose, sílica, talco, amido oxidado, gelatina, estearato de magnésio e cera de palma.
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The Placebo capsule supplement was taken for 4 weeks (6 capsules per day).
The Beta-Alanine capsule supplement was taken for 4 weeks, with a daily dosage of 4.8 g of Beta-Alanine (equivalent to 6 capsules per day, each containing 800 mg of Beta-Alanine).
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Experimental: Beta-Alanine
Each capsule containing 800 mg of Beta-Alanine.
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The Placebo capsule supplement was taken for 4 weeks (6 capsules per day).
The Beta-Alanine capsule supplement was taken for 4 weeks, with a daily dosage of 4.8 g of Beta-Alanine (equivalent to 6 capsules per day, each containing 800 mg of Beta-Alanine).
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O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
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Specific Wrestling Performance Test (SWPT)
Prazo: Including for 4 days in both beta-alanine and placebo trials
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The test consists of two rounds with identical procedures.
Each round lasts for 3 minutes, with a 30-second rest interval between rounds.
During the first minute, participants perform one throw every 10 seconds for a total of 3 throws.
This is followed by maximal repeated throws performed between 30 and 50 seconds, and then a rest period from 50 to 60 seconds.
The second minute follows the same procedure as the first minute.
In the third minute, participants again perform one throw every 10 seconds for a total of 3 throws, followed by 30 seconds of maximal repeated throws, during which the total number of throws is recorded.
According to the experimental design of Marković, the dummy weight is adjusted based on the athlete's body weight: participants weighing less than 75 kg throw a 22 kg dummy, those weighing between 75-90 kg throw a 27 kg dummy, and those weighing more than 90 kg throw a 32 kg dummy (Marković et al., 2022).
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Including for 4 days in both beta-alanine and placebo trials
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Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
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Reaction test
Prazo: Including for 4 days in both beta-alanine and placebo trials
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Reaction time is a key factor influencing wrestling performance, as shorter reaction times enable athletes to execute more effective technical and tactical actions.
In this study, the BlazePod reaction light system will be used to conduct the reaction test.
After hearing the command "Ready," participants will assume a position with both hands and knees on the ground.
Once the light is activated, participants must stand up as quickly as possible and tap the reaction light.
The time interval between the "Ready" command and the light activation will vary randomly in order to prevent participants from anticipating the timing of the stimulus.
The test will be performed three times with a 1-minute rest interval between trials, and the best performance result will be recorded.
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Including for 4 days in both beta-alanine and placebo trials
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Grip strength test
Prazo: Including for 4 days in both beta-alanine and placebo trials
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Grip strength will be assessed using an electronic handgrip dynamometer.
Participants will stand in a natural upright position with their arms hanging naturally at their sides.
The elbows and wrists will be maintained at 0° extension, and the grip width will be adjusted to fit the position of the second finger joint.
During the test, participants will be instructed to squeeze the dynamometer handle as forcefully as possible for 5 seconds.
Grip strength measurements will be performed three times for each hand, with a 1-minute rest interval between trials.
The highest value obtained will be recorded as the test result.
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Including for 4 days in both beta-alanine and placebo trials
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The Borg Rating of Perceived Exertion (RPE) Scale
Prazo: Including for 4 days in both beta-alanine and placebo trials
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The Borg Rating of Perceived Exertion Scale measures how hard exercise feels.
Participants rate effort from 6 (no exertion) to 20 (maximal exertion).
A higher score means greater effort (worse fatigue).
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Including for 4 days in both beta-alanine and placebo trials
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Medicine Ball Chest Throw (MBCT) test
Prazo: Including for 4 days in both beta-alanine and placebo trials
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The sport-specific wrestling fitness test protocol developed by Dehnou in 2020 will be used in this study.
Participants will sit on a chair with their feet shoulder-width apart and firmly placed on the floor, with the toes aligned with the starting line.
The knees will be maintained at a 90° flexion angle while the upper body remains upright.
Participants will hold a 5 kg medicine ball in front of the chest with both hands.
During the test, participants will forcefully push the ball forward using a chest-pass motion similar to a basketball chest pass.
Throughout the movement, the ischial tuberosities must remain in contact with the seat, and trunk rotation is not permitted.
The throwing distance will be measured and recorded.
The test will be performed three times with a 1-minute rest interval between trials, and the greatest distance achieved will be recorded as the final result.
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Including for 4 days in both beta-alanine and placebo trials
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Overhead Medicine Ball Throw (OMBT) test
Prazo: Including for 4 days in both beta-alanine and placebo trials
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The sport-specific wrestling fitness test protocol developed by Dehnou in 2020 will be adopted in this study.
Participants will stand with their feet shoulder-width apart and their heels aligned with the starting line, while holding a 5 kg medicine ball naturally in front of the body with both hands.
Participants will then squat down until the medicine ball reaches knee level, after which they will rapidly extend the body and forcefully throw the ball backward over the head.
The throwing distance will be measured and recorded.
The test will be performed three times with a 1-minute rest interval between trials, and the greatest distance achieved will be recorded as the final result.
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Including for 4 days in both beta-alanine and placebo trials
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Back strength test
Prazo: Including for 4 days in both beta-alanine and placebo trials
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Back strength will be measured using a back strength dynamometer.
Participants will stand on the testing platform while gripping the handle with both hands using an overhand grip.
The knees will remain fully extended, and the upper body will lean forward at approximately 30°.
The length of the chain attached to the handle may be adjusted according to each participant's body size to ensure an appropriate testing position.
During the test, participants will pull the handle upward with maximal effort using the strength of the back and upper body muscles, while avoiding excessive use of the arms and legs.
The dynamometer pointer will display the measured back strength value.
The test will be performed three times with a 1-minute rest interval between trials, and the highest value obtained will be recorded.
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Including for 4 days in both beta-alanine and placebo trials
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Colaboradores e Investigadores
É aqui que você encontrará pessoas e organizações envolvidas com este estudo.
Patrocinador
Colaboradores
Investigadores
- Cadeira de estudo: Jung-Piao Tsao, China Medical University, China
Datas de registro do estudo
Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.
Datas Principais do Estudo
Início do estudo (Real)
11 de abril de 2026
Conclusão Primária (Real)
24 de maio de 2026
Conclusão do estudo (Estimado)
1 de outubro de 2026
Datas de inscrição no estudo
Enviado pela primeira vez
8 de junho de 2026
Enviado pela primeira vez que atendeu aos critérios de CQ
8 de junho de 2026
Primeira postagem (Real)
11 de junho de 2026
Atualizações de registro de estudo
Última Atualização Postada (Real)
11 de junho de 2026
Última atualização enviada que atendeu aos critérios de controle de qualidade
8 de junho de 2026
Última verificação
1 de junho de 2026
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- CMUH114-REC3-170
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
NÃO
Informações sobre medicamentos e dispositivos, documentos de estudo
Estuda um medicamento regulamentado pela FDA dos EUA
Não
Estuda um produto de dispositivo regulamentado pela FDA dos EUA
Não
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