Traditional Versus Cluster Resistance Training in Striking Combat Sport Athletes (TRG-CLG)
2026年6月11日 更新者:Amador García Ramos、Universidad de Granada
Effects of Traditional and Cluster Resistance Training Using Four Multi-Joint Exercises on Neuromuscular Performance in Striking Combat Sport Athletes
This randomized controlled trial compared the effects of traditional and cluster resistance training on neuromuscular performance in amateur striking combat sport athletes.
Twenty-eight athletes completed a 6-week full-body resistance training program including squat, bench press, deadlift, and bench pull exercises.
Participants were assigned to either a traditional training group, which performed repetitions continuously, or a cluster training group, which incorporated short intra-set rest periods.
Neuromuscular performance was assessed before and after the intervention through countermovement jump height, medicine-ball throw distance, and load-velocity relationship variables obtained from the four resistance exercises.
The study aimed to determine whether cluster resistance training provides superior neuromuscular adaptations compared with traditional resistance training when training volume and relative intensity are matched.
研究概览
研究类型
介入性
注册 (实际的)
32
阶段
- 不适用
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习地点
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Concepción、智利
- Universidad Católica de la Santísima Concepción
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参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
- 孩子
- 成人
接受健康志愿者
是的
描述
Inclusion Criteria:
- Healthy men and women aged 18 years or older. Active participation in striking combat sports (boxing, kickboxing, or karate) for at least 3 years.
- Minimum of 1 year of experience with the resistance exercises included in the study (squat, bench press, deadlift, and bench pull).
- Willingness to refrain from participating in additional strength training programs during the study period.
- Provision of written informed consent.
Exclusion Criteria:
- Presence of any musculoskeletal injury during the 6 months preceding data collection.
- Any medical condition that could contraindicate participation in resistance training.
- Failure to complete the training intervention or testing procedures.
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 主要用途:基础科学
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:单身的
武器和干预
参与者组/臂 |
干预/治疗 |
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有源比较器:Traditional
Participants performed a 6-week full-body resistance training program consisting of squat, bench press, deadlift, and bench pull exercises.
Training was conducted twice per week and included 3 sets of 8 repetitions at 75% of the individual one-repetition maximum (1RM) for each exercise.
Participants completed all repetitions consecutively within each set without intra-set rest periods.
Inter-set rest intervals were 3 minutes and inter-exercise rest intervals were 5 minutes.
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Participants completed a 6-week full-body resistance training program consisting of squat, bench press, deadlift, and bench pull exercises.
Training was performed twice weekly and included 3 sets of 8 repetitions at 75% of the individual one-repetition maximum (1RM) for each exercise.
All repetitions within a set were performed consecutively without intra-set rest periods.
Participants were instructed to execute the concentric phase of each repetition with maximal intended velocity.
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实验性的:Cluster
Participants performed the same 6-week full-body resistance training program as the traditional training group, consisting of squat, bench press, deadlift, and bench pull exercises performed twice per week.
Training included 3 sets of 8 repetitions at 75% of the individual one-repetition maximum (1RM) for each exercise.
The repetitions were organized into clusters of two repetitions separated by 15-second intra-set rest intervals (2 + 2 + 2 + 2 repetitions).
Inter-set rest intervals were 3 minutes and inter-exercise rest intervals were 5 minutes.
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Participants completed a 6-week full-body resistance training program consisting of squat, bench press, deadlift, and bench pull exercises.
Training was performed twice weekly and included 3 sets of 8 repetitions at 75% of the individual one-repetition maximum (1RM) for each exercise.
Repetitions were organized into clusters of two repetitions separated by 15-second intra-set rest intervals (2 + 2 + 2 + 2 repetitions).
Participants were instructed to execute the concentric phase of each repetition with maximal intended velocity.
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
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Load-velocity relationship (LVR).
大体时间:Baseline and after 6 weeks of resistance training
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Individual LVR were determined for the squat, bench press, and bench pull exercises using a Smith machine (FFittech, Taiwan, China), whereas the deadlift exercise was performed with a hexagonal barbell.
Each test started with an initial external load of 20 kg, which was progressively increased until the mean velocity (MV) of the fastest repetition differed by less than 0.30 m·s-1 from the theoretical MV associated with the 1RM of each exercise (0.30 m/s for squat, 0.15 m/s for deadlift, 0.17 m/s for bench press, and 0.50 m/s for bench pull) (Weakley et al., 2021).
The load increments were adjusted according to the exercise and movement velocity to ensure an appropriate distribution of loads across the individual force-velocity spectrum.
Three repetitions were performed at lighter loads, whereas only two repetitions were completed at heavier loads.
A standardized rest interval of 10 seconds was provided between repetitions at the same load.
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Baseline and after 6 weeks of resistance training
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
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Countermovement jump
大体时间:Baseline and after 6 weeks of resistance training
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Participants completed three CMJ attempts with a 1-minute recovery period between trials.
From a standing position with feet approximately shoulder-width apart and hands placed on the hips, participants performed a rapid countermovement to a self-selected depth and immediately executed a maximal vertical jump.
Jump height was estimated from flight time using the equation: height = (flight time2 × 9.81 m·s-2) / 8, where 9.81 m·s-2 corresponds to gravitational acceleration.
Flight time was recorded using an infrared optical measurement system (OptoJump, Microgate, Bolzano, Italy).
Participants were instructed to maintain their hands on the hips during the entire movement and to land with the lower limbs fully extended.
Trials not complying with these technical requirements were discarded and repeated after 1 minute of rest under the supervision of the same experienced evaluator.
The best performance obtained across the three trials was retained for subsequent analyses.
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Baseline and after 6 weeks of resistance training
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Medicine ball throw (MBT).
大体时间:Baseline and after 6 weeks of resistance training
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Upper-body explosive performance was evaluated using a seated MBT test performed with a 3-kg medicine ball.
Testing was conducted indoors on a hardwood surface.
Participants sat behind a marked line with both feet in contact with the floor and executed a single-arm forward chest-pass action from a stable seated position.
Throws were performed separately with the dominant and non-dominant arms, using a coordinated movement involving the trunk and upper-limb musculature.
Throwing distance was determined as the linear distance between the starting line and the first point of ball contact with the floor, measured with a tape measure.
Three maximal attempts were completed with each arm, with 1 minute of recovery between trials.
The greatest distance achieved with each arm was retained for subsequent statistical analyses.
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Baseline and after 6 weeks of resistance training
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合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (实际的)
2024年9月4日
初级完成 (实际的)
2025年3月6日
研究完成 (实际的)
2025年3月6日
研究注册日期
首次提交
2026年6月11日
首先提交符合 QC 标准的
2026年6月11日
首次发布 (实际的)
2026年6月17日
研究记录更新
最后更新发布 (实际的)
2026年6月17日
上次提交的符合 QC 标准的更新
2026年6月11日
最后验证
2026年6月1日
更多信息
与本研究相关的术语
其他研究编号
- UGR-TRG-CLG-2024
- 25KJA180002 (其他赠款/资助编号:Major Project of Basic Science (Natural Science) Research in Jiangsu Higher Education Institutions)
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
不
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研究美国 FDA 监管的药品
不
研究美国 FDA 监管的设备产品
不
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