Effects of Blood Flow Restriction Training on Neuromuscular Function and Performance in Artistic Jump Rope Athletes

Официальное название

Effects of Blood Flow Restriction Training on Upper and Lower Limb Neuromuscular Function, Body Composition, Physiological Responses, and Sport Performance in Artistic Jump Rope Athletes: A Randomized Controlled Trial

Обзор

The goal of this randomized controlled trial is to investigate whether blood flow restriction training can improve physical function and sports performance in artistic jump rope athletes. The study will include 30 healthy artistic jump rope athletes aged 18 to 25 years. The main questions this study aims to answer are: 1. Does blood flow restriction training improve neuromuscular function compared with conventional training? 2. Does blood flow restriction training improve muscle strength, power, body composition, physiological responses, and artistic jump rope performance? Researchers will compare participants receiving blood flow restriction training with participants performing conventional training to determine whether blood flow restriction training provides additional benefits. Participants will complete an 8-week training program and undergo assessments before and after the intervention, including muscle function tests, physical performance tests, body composition measurements, and physiological response evaluations.

Подробное описание

Blood flow restriction (BFR) training is an exercise method that uses external pressure to partially restrict blood flow during exercise. This method may allow individuals to achieve improvements in muscle function and physical performance while using lower exercise loads. However, the effects of BFR training in artistic jump rope athletes are not fully understood.

The purpose of this study is to examine the effects of an 8-week blood flow restriction training program on neuromuscular function, body composition, physiological responses, and sport-specific performance in artistic jump rope athletes.

Approximately 30 healthy artistic jump rope athletes aged 18 to 25 years will participate in this study. Participants will be randomly assigned to either a blood flow restriction training group or a conventional training group. Both groups will continue their regular artistic jump rope training during the intervention period. The blood flow restriction training group will complete selected training sessions with individualized blood flow restriction pressure.

Before and after the 8-week intervention, researchers will assess changes in neuromuscular function, upper and lower limb muscle strength, explosive power, jump rope-specific performance, body composition, heart rate responses, and blood lactate responses.

This study may provide information about whether blood flow restriction training can be used as an effective training strategy to improve physical function and performance characteristics in artistic jump rope athletes.

Вмешательства

• Поведенческое Blood Flow Restriction Training
  An 8-week blood flow restriction training program combined with regular artistic jump rope training. External pressure will be applied using a blood flow restriction device during selected training sessions.
• Поведенческое Conventional Artistic Jump Rope Training
  An 8-week conventional artistic jump rope training program without blood flow restriction.

Первичные конечные точки

• Change in Neuromuscular Function Assessed by Surface Electromyography and Maximal Voluntary Contraction [Срок оценки: Baseline and after 8 weeks of intervention]

Вторичные конечные точки (9)

• Change in Upper Limb Muscle Strength Assessed by Hand Grip Strength Test [Срок оценки: Baseline and after 8 weeks of intervention]
• Change in One-Repetition Maximum Strength [Срок оценки: Baseline and after 8 weeks of intervention]
• Change in Lower Limb Explosive Power Assessed by Three-Dimensional Force Platform [Срок оценки: Baseline and after 8 weeks of intervention]
• Change in Upper Limb Anaerobic Power During Wingate Test [Срок оценки: Baseline and after 8 weeks of intervention]
• Change in Lower Limb Anaerobic Power During Wingate Test [Срок оценки: Baseline and after 8 weeks of intervention]
• Change in Body Composition Assessed by Dual-Energy X-ray Absorptiometry [Срок оценки: Baseline and after 8 weeks of intervention]
• Change in Physiological Responses During Exercise [Срок оценки: Baseline and 8 weeks after intervention]
• Change in Dynamic Balance Performance [Срок оценки: Baseline and 8 weeks after intervention]
• Change in Short-Duration Rope Turning Performance [Срок оценки: Baseline and after 8 weeks of intervention]

Критерии участия

Критерии включения

• Adults aged 18 to 25 years.
• Current artistic jump rope athletes with at least 2 years of regular artistic jump rope training experience.
• Participants who are able to perform artistic jump rope skills and complete all study-related assessments and training procedures.
• Participants who are physically healthy and have no medical conditions that may interfere with exercise testing or blood flow restriction training.
• Participants who have no acute or chronic musculoskeletal injuries affecting the upper limbs, lower limbs, or trunk.
• Participants who voluntarily agree to participate and provide written informed consent before enrollment.

Критерии исключения

• Participants younger than 18 years or older than 25 years.
• Presence of cardiovascular disease, peripheral vascular disease, respiratory disease, neurological disease, metabolic disease, coagulation disorders, history of thrombosis, severe varicose veins, severe hypertension, or other conditions that may affect exercise safety.
• Presence of acute or chronic musculoskeletal injuries, including injuries involving muscles, joints, ligaments, tendons, or bones, that prevent safe completion of study procedures.
• Significant pain, severe fatigue, insufficient recovery, poor sleep condition, or other health conditions that may affect exercise performance or participant safety.
• Use of medications, nutritional supplements, or sports supplements within the previous week that may influence cardiovascular function, muscle metabolism, blood lactate response, heart rate variability, neuromuscular activation, fatigue response, or exercise performance.
• Skin damage, infection, dermatological disorders, severe allergy history, or other conditions affecting blood flow restriction cuff application or surface electromyography electrode placement.
• Inability to understand the study procedures or inability to complete required assessments, including physical performance tests, blood flow restriction training, or blood lactate testing.
• Refusal to participate in blood flow restriction training or withdrawal of informed consent during the study.

Критерии исключения

• 1\. Age younger than 18 years or older than 25 years. 2. Presence of cardiovascular disease, peripheral vascular disease, respiratory disease, neurological disease, metabolic disease, coagulation abnormalities, history of thrombosis, severe varicose veins, severe hypertension, or other conditions that may affect exercise testing or blood flow restriction training safety.

3\. Current acute or chronic injuries involving muscles, joints, ligaments, tendons, or bones that prevent safe completion of study procedures.

4\. Severe fatigue, poor recovery status, significant pain, insufficient sleep, or other conditions that may influence exercise performance or participant safety.

5\. Use of medications, nutritional supplements, or sports supplements that may affect cardiovascular function, muscle metabolism, blood lactate response, heart rate variability, neuromuscular activation, fatigue response, or exercise performance within the previous week.

6\. Skin damage, infection, dermatological disorders, severe allergy history, or other conditions affecting blood flow restriction cuff application or surface electromyography electrode placement.

7\. Inability or unwillingness to complete study assessments, blood flow restriction training, blood lactate testing, or other required procedures.

8\. Withdrawal of consent or inability to comply with the study protocol during the intervention period.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Да

Дизайн исследования

Распределение

Рандомизированное

Модель

Параллельные группы

Маскирование

Открытое

Основная цель

Другое

Центры проведения

Китай · 1 центр

• Shanghai University of Sport, School of Physical EducationKun — Шанхай

Идентификаторы

NCT: NCT07750977 · 102772026RT119

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

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