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Clinical Trials in China / NCT07740096
Active, not recruiting Not applicable

Effects of Microdosed Plyometric Training on Lower-Limb Neuromuscular Function and Sport-Specific Performance in Rope-Skipping Athletes

NCT07740096 · tracked via the Priya Life Science China tracker
Sponsor
Chongqing Normal University
Phase
Not applicable
Started
2026-06-01
Last updated
2026-07-31

Condition(s) studied

Athletic Performance Enhancement

Investigational drug(s) / intervention(s)

Microdosed Plyometric TrainingTraditional Concentrated Plyometric Training

Microdosed Plyometric Training: Participants assigned to this intervention will continue their regular rope-skipping-specific training and complete an 8-week microdosed plyometric training program. Plyometric training will be distributed across five sessions per week using a high-frequency, short-duration format. The exercise content, total weekly training duration, total weekly jump contacts, and progression principles will be matched as closely as possible to the traditional concentrated plyometric training intervention. The primary difference between the interventions will be training frequency and the amount of training completed in each session.

Traditional Concentrated Plyometric Training: Participants assigned to this intervention will continue their regular rope-skipping-specific training and complete an 8-week traditional concentrated plyometric training program. Plyometric training will be performed in two concentrated sessions per week. The exercise content, total weekly training duration, total weekly jump contacts, and progression principles will be matched as closely as possible to the microdosed plyometric training intervention. The primary difference between the interventions will be training frequency and the amount of training completed in each session.

Study summary

The goal of this clinical trial is to compare two ways of scheduling plyometric training in rope-skipping athletes. The study will examine whether short and frequent training sessions have different effects on lower-limb muscle function, rope-skipping performance, and perceived fatigue compared with longer training sessions performed less often.

Approximately 60 rope-skipping athletes will be randomly assigned to one of two groups. Both groups will continue their regular rope-skipping training and complete an additional 8-week plyometric training program. One group will perform short plyometric training sessions five days per week. The other group will perform concentrated plyometric training sessions twice per week. The exercise content, weekly training volume, and training progression will be kept as similar as possible between the two groups.

Researchers will assess lower-limb muscle function and rope-skipping-specific performance before and after the intervention. Training attendance, completion, perceived exertion, muscle soreness, and adverse events will also be recorded. The study aims to determine whether distributing plyometric training across more frequent and shorter sessions produces different training effects from concentrating the training into fewer sessions.

Eligibility

Sex
ALL
Min age
18 Years
Max age
25 Years
Healthy volunteers
Accepted
Inclusion Criteria: * \* Rope-skipping athletes with at least 1 year of rope-skipping training experience * Able to complete regular rope-skipping training and all study-related testing procedures * No severe lower-limb sports injury within the previous 3 months * No cardiovascular disease, neurological disease, or other contraindication to exercise * Willing to participate voluntarily and provide written informed consent * For participants who are minors, written informed consent must also be obtained from a parent or legal Exclusion Criteria: * \* Participation in additional systematic strength training or plyometric training during the intervention period * Insufficient adherence to the prescribed training program * Injury, physical discomfort, or another condition occurring during testing or intervention that prevents continued participation in the study

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Chengdu College of Arts and Sciences Chongqing Chongqing Municipality

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07740096 on ClinicalTrials.gov ↗ ← All trials in China