- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06468449
Strength Training on Muscle Power Output and Neuromuscular Adaptation Among China University Long Jump Athletes
Effects of Optimal Load Strength Training on Muscle Power Output and Neuromuscular Adaptation During Takeoff Among China University Long Jump Athletes
The purpose of this study is to investigate the effects of optimal load strength training on the lower limb neuromuscular adaptation of athletes. An anatomical analysis of the vertical jump reveals three phases: the propulsion phase, the flight phase, and the landing phase.
This study is an 8-week randomized controlled trial. After selecting the participants, basic information such as height, weight, age, and years of training experience is collected. Subsequently, a maximal output power test for lower limb squatting is conducted. Participants are then randomly assigned to the speed group, power group, and strength group. The optimal power load for the power group is determined based on the participant maximal output power. Training plans are developed for the traditional group, power group, and strength group. Each training session is organized and supervised by a designated person. Surface electromyography, three-dimensional motion capture systems, and force platforms are used to collect electromyographic and kinetic data of participants during pre-test and post-test vertical jump actions. Electromyography evoked potential instruments and myotonometer are used to collect nerve signals of the tibial nerve (posterior calf) and muscle fiber dimension data of the rectus femoris before and after the experiment. Additionally, static full-range-of-motion vertical jump kinematics and kinetics data are collected before and after the experiment. To ensure the quality and validity of the intervention, the following controls are implemented during the experiment: first, communication with the participants to inform them of the purpose of the study and ensure adherence to the correct movement standards during testing; second, having a designated person responsible for resistance training during the experiment; third, using the same equipment and team for testing to maximize the controllability of the experiment process; fourth, providing verbal encouragement to participants during testing to maximize effort and minimize experimental errors. The aim is to determine the effects of optimal load strength training on improving the lower limb output power during the propulsion phase of the take-off stage in long jump athletes and the underlying neuromuscular adaptation mechanisms.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
HeiBei
-
QinHuangdao, HeiBei, China, 066004
- YanShan university
-
Qinhuangdao, HeiBei, China, 066400
- Rong Wenchao
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Aim for uniformity in various indicators to minimize errors caused by height, weight, and training experience differences.
- Aim for a 1RM/body weight ratio of around 2.
- Maintain normal diet and sleep patterns during the training period, and refrain from using supplements such as creatine and protein powder.
- Male university long jump athletes should be aged ≥18, and they should not have engaged in strength training 48 hours before the baseline testing.
Exclusion Criteria:
- Participants with various visceral diseases and abnormal liver or kidney function are excluded.
- Those with unhealthy habits are excluded.
- Participants with caffeine intake within 3 hours before testing are excluded.
- Individuals who have engaged in high-intensity resistance exercises within the past 24 hours are excluded.
- Those with lower limb joint injuries (open and closed) in the last 3 months are excluded.
- Participants with contraindications such as cardiovascular diseases, skin allergies, and hernia are excluded.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Sequential Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental Group:power output
by identifying the optimal load at which the athlete achieves the highest power output.
The training program is then tailored based on these measurements, ensuring that the athlete trains at the load that maximizes their power output.
This approach allows for more efficient and effective strength training, potentially leading to improved athletic performance.
Throughout the training period, the VBT equipment continuously monitors the athlete's performance, providing real-time feedback and allowing for adjustments to the load as the athlete's strength and power improve.
The goal is to enhance neuromuscular adaptations and optimize the athlete's power development, particularly during explosive movements like the vertical jump and long jump.
|
Lower limb power output training content: Half squat up squat: 70%1R (6 repetitions × 5sets) + 5 knees jumps × 5 sets with an interval of 90 seconds; |
|
Experimental: Control Group:speed combined force
Speed combined with strength training is designed to enhance the explosive power of long jumpers' lower limbs.
This involves using maximum strength barbell squats and knee jumps to develop athletes' maximum strength and improve the speed of their neural contractions.
Additionally, plyometric exercises and sprint drills are incorporated to further boost explosive power and coordination.
This comprehensive training approach aims to optimize both the force and velocity aspects of power, leading to better overall performance in explosive movements critical for long jump success.
Regular assessments and adjustments ensure that training loads are appropriate and effective for each athlete's progress.
|
Lower limb Force Combined Speed training content: Rapid half squat : Optimal load (6 sets × 7 repetitions). Rest intervals between sets range from 2 to 5 minutes. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Indicators of Neurological Adaptation(Number of nerve impulses)
Time Frame: From enrollment to the end of treatment at 8 weeks
|
This includes the number of nerve impulses.
Using wireless electromyography signal collection system
|
From enrollment to the end of treatment at 8 weeks
|
|
Muscle adaptation indicators (Muscle cross-sectional area)
Time Frame: From enrollment to the end of treatment at 8 weeks
|
Muscle cross-sectional area assessment uses ultrasound to measure the cross-sectional area of the rectus femoris muscle fibers to assess muscle adaptation
|
From enrollment to the end of treatment at 8 weeks
|
|
Sports performance indicators (Vertical jump speed )
Time Frame: From enrollment to the end of treatment at 8 weeks
|
This study used three-dimensional motion capture equipment and a test bench to test the vertical jump speed of athletes.
|
From enrollment to the end of treatment at 8 weeks
|
|
Sports performance indicators (Power output)
Time Frame: From enrollment to the end of treatment at 8 weeks
|
This study used three-dimensional motion capture equipment and a test bench to test the power output of athletes' lower limbs.
|
From enrollment to the end of treatment at 8 weeks
|
|
Sports performance indicators (Take-off height)
Time Frame: From enrollment to the end of treatment at 8 weeks
|
This study used three-dimensional motion capture equipment and a test bench to test the athletes' take-off height before and after the experiment.
|
From enrollment to the end of treatment at 8 weeks
|
|
Indicators of Neurological Adaptation ( Nerve impulse frequency)
Time Frame: From enrollment to the end of treatment at 8 weeks
|
This includes nerve impulse frequency,Using wireless electromyography signal collection system
|
From enrollment to the end of treatment at 8 weeks
|
|
Indicators of Neurological Adaptation (M wave amplitude)
Time Frame: From enrollment to the end of treatment at 8 weeks
|
This includes the M wave amplitude,The test was performed using a potential evoked instrument.
|
From enrollment to the end of treatment at 8 weeks
|
|
Indicators of Neurological Adaptation (H-max/ M-max)
Time Frame: From enrollment to the end of treatment at 8 weeks
|
This includes the H-max/ M-max.
The test was performed using a potential evoked instrument.
Among them, M-max refers to the average value of the first ten M-wave amplitude peaks.
H-max refers to the maximum value of the H wave observed when the sensory nerve is stimulated at a frequency of 1Hz.
|
From enrollment to the end of treatment at 8 weeks
|
|
Indicators of Neurological Adaptation (Nerve conduction velocity)
Time Frame: From enrollment to the end of treatment at 8 weeks
|
Nerve conduction velocity.
The test was performed using a potential evoked instrument.
|
From enrollment to the end of treatment at 8 weeks
|
|
Indicators of Neurological Adaptation (Latency of the H reflex)
Time Frame: From enrollment to the end of treatment at 8 weeks
|
Latency of the H reflex.
The test was performed using a potential evoked instrument.
|
From enrollment to the end of treatment at 8 weeks
|
|
Indicators of Neurological Adaptation (presynaptic inhibition)
Time Frame: From enrollment to the end of treatment at 8 weeks
|
This includes presynaptic inhibition.
This value can only be obtained by processing the H reflex amplitude and the M wave amplitude.
The presynaptic inhibition calculation formula is: Hmax1Hz = (Ave.
H1:H10) / H1 PSI = Hmax1Hz / Mmax.
|
From enrollment to the end of treatment at 8 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: wenchao rong, Ph.D, University Putra Malaysia
Publications and helpful links
Helpful Links
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 (Actual)
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
- 2024Y004
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
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