跳至主要内容
临床试验/NCT05586451
NCT05586451已完成不适用

Muscle Activation With Acute Bouts of Blood Flow Restricted Resistance Exercise Compared to High Load Resistance Exercise in Trained Versus Untrained Adults

Louisiana State University and A&M College2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2022年7月5日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
30
试验地点
2
主要终点
Muscle Activation Measured During Traditional High Load Resistance Exercise (HLRE)

研究概览

简要总结

Blood flow restricted (BFR) resistance exercise has been shown to improve skeletal muscle adaptations to low load resistance exercise. One of many adaptations with resistance training is neural adaptations that occur within the first few weeks of resistance training. It has been hypothesized that these neural adaptations are blunted when using blood flow restricted exercise. Therefore, the investigators propose to examine the muscle activation created by resistance exercise with different intensities with blood flow restriction and without blood flow restriction in sedentary compared to resistance-trained individuals. The investigators will recruit and completely study up to 30, previously untrained and resistance-trained, healthy, college-aged (18-40 years) males. Participants will come in the laboratory for 5 total visits. These visits will consist of a screening/familiarization visit, a strength testing visit, and 3 acute exercise visits. The acute exercise visits will consist of 2 blood flow restricted resistance sessions at different intensities and a traditional high load resistance exercise session. The 3 acute exercise visits will be randomized. The investigators will measure muscle mass (appendicular lean mass) using Dual Energy X-Ray Absorptiometry, muscle strength and endurance using isotonic and isokinetic testing, and muscle activation using surface electromyography. The investigators will also use near infrared spectroscopy (NIRS) to measure the muscle tissue (oxygen) saturation index (TSI) in the vastus lateralis during exercise. Finally, the investigators will also draw blood before and after each exercise session to measure hormones, metabolites, and markers of inflammation using commercially available assays (e.g., ELISAs).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
None

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
Male
接受健康志愿者

入选标准

  • Capable and willing to give written informed consent
  • Capable of understanding inclusion and exclusion criteria
  • 18-40 years of age
  • A waist circumference < 40 inches.
  • No medical condition that would limit their participation in supervised exercise sessions based on the Physical Activity Readiness Questionnaire for Everyone (PARQ+)
  • No current prescription medications
  • Willing to allow researchers to use data and images (e.g., Dual Energy X-Ray Absorptiometry) for research purposes after study participation is completed
  • Either untrained or resistance-trained by the following definitions: Untrained individuals are considered those that report less than two days per week of structured (> 30 minutes) moderate to vigorous-intensity aerobic exercise and less than two days per week of structured resistance training for the 3 months prior to study start. Resistance-trained individuals are considered those who report performing structured moderate to intense resistance exercise for at least three days per week for at least 2 years prior to study start.

排除标准

  • Self-report history of diabetes mellitus
  • Self-report history of cardiovascular, peripheral vascular, cerebral vascular, pulmonary, or renal disease
  • Self-report or evidence of uncontrolled hypertension > 150/85 (or measured)
  • Self-report history of blood clotting disorders
  • Self-report history of deep vein thrombosis or pulmonary embolism
  • Self-report history of sickle cell trait
  • Self-report history of varicose veins
  • Self-report history of a myopathy leading to muscle loss, weakness, severe cramps or myalgia
  • Self-report history of orthopedic limitations that would preclude them from participation in a dynamic exercise program
  • Self-report history of musculoskeletal disorders (e.g., severe osteoarthritis, rheumatoid arthritis, avascular necrosis or osteonecrosis)
  • Self-report history of neurological disorders (e.g., peripheral neuropathy, amyotrophic lateral sclerosis, multiple sclerosis, fibromyalgia, Parkinson's disease)
  • Weight loss of > 10% in the last 3 months prior to screening
  • Active tobacco use including smoking, vaping, or smokeless tobacco use
  • Current consumption of > 14 alcoholic drinks per week based on self-report
  • Any other condition that, in the judgement of the Principal Investigator and/or the Medical Director of this protocol, may interfere with study participation and adherence to the protocol

结局指标

主要结局

Muscle Activation Measured During Traditional High Load Resistance Exercise (HLRE)

时间窗: Measurement will occur during the acute bout HLRE, which will occur during the HLRE study visit.

Muscle (vastus lateralis) activation will be measured using surface EMG, during the knee extension exercises conducted during the acute HLRE bout.

Low Load Resistance Exercise with Blood Flow Restriction (LLBFR)

时间窗: Measurement will occur during the acute bout LLBFR, which will occur during the LLBFR study visit.

Muscle (vastus lateralis) activation will be measured using surface EMG, during the knee extension exercises conducted during the acute LLBFR bout.

Moderate Load Resistance Exercise with Blood Flow Restriction (MLBFR)

时间窗: Measurement will occur during the acute bout MLBFR, which will occur during the MLBFR study visit.

Muscle activation (vastus lateralis) will be measured using surface EMG, during the knee extension exercises conducted during the acute MLBFR bout.

次要结局

  • Change in Maximal Voluntary Contraction following LLBFR(Measurements will be conducted before and immediately following the completion of the LLBFR bout.)
  • Change in Maximal Voluntary Contraction following HLRE(Measurements will be conducted before and immediately following the completion of the HLRE bout.)
  • Change in Maximal Voluntary Contraction following MLBFR(Measurements will be conducted before and immediately following the completion of the MLBFR bout.)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Brian Irving

Associate Professor

Louisiana State University and A&M College

研究点 (2)

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