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临床试验/NCT03723226
NCT03723226已完成不适用

Impact of Low-Intensity Resistance Exercise With and Without Blood Flow Redistricted (BFR) on Muscle Mitochondrial Oxidative Capacity

Louisiana State University and A&M College1 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2019年1月28日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
24
试验地点
1
主要终点
Changes in Mitochondrial Oxidative Capacity

研究概览

简要总结

Blood flow restricted (BFR) exercise has been shown to improve skeletal muscle adaptations to resistance exercise. BFR uses blood pressure cuffs (i.e., tourniquets) to reduce skeletal muscle blood flow during resistance exercise. One benefit of BFR is that skeletal muscle adaptations to resistance exercise training including muscle hypertrophy and increases in strength can be achieved at lower-loads (e.g., 25-30% 1RM), that are often comparable to more traditional resistance training loads (70-85% 1RM). However, the impact that low-load BFR resistance exercise has on muscle quality and bioenergetics is unknown. The present study will examine the impact of 6 weeks of low-load, single-leg resistance exercise training with or without personalized BFR on measures of muscle mass, strength, quality, and mitochondrial bioenergetics. The investigators will recruit and study up to 30, previously sedentary, healthy, college-aged adults (18-40 years). The investigators will measure muscle mass using Dual Energy X-Ray Absorptiometry and muscle strength and endurance using isokinetic testing. The investigators will normalize knee extensor strength to lower limb lean mass to quantify muscle quality. The investigators will also use near infrared spectroscopy (NIRS) to measure mitochondrial oxidative capacity in the vastus lateralis. Finally, the investigators will measure markers of systemic inflammation and markers of muscle damage using commercially available ELISA assays.

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
All
接受健康志愿者
是

入选标准

  • •Capable and willing to give written informed consent
  • •Capable of understanding inclusion and

排除标准

  • •18-40 years of age inclusive
  • •Body Mass Index (BMI) between 18.5-30 kg/m2 inclusive
  • •No medical condition that would limit their participation in supervised exercise training based on the Physical Activity Readiness Questionnaire for Everyone (PARQ+)
  • •No current prescription medications, with the exception of birth control
  • •Willing to allow researchers to use data, biospecimens (e.g., blood) and images (e.g., Dual Energy x-Ray Absorptiometry) for research purposes after study participation is completed
  • •Exclusion Criteria.
  • •Evidence or self-report being pregnant, lactating, or anticipating becoming pregnant in the next year
  • •Participation in resistance or aerobic exercise training > 2 days per week within the 3 months prior to screening
  • •Self-report of history of type 1 or 2 diabetes mellitus
  • •Self-report history of cardiovascular, peripheral vascular, cerebral vascular, pulmonary, or renal disease
  • •Self-report or evidence of uncontrolled hypertension
  • •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 smoking
  • •Current consumption of > 14 alcoholic drinks per week based on self-report
  • •Absolute Contraindication to Exercise as Defined by the American College of Sports Medicine,1 including:
  • •Resting diastolic blood pressure > 100 mm Hg
  • •Resting systolic blood pressure > 180 mm Hg
  • •Resting heart rate > 100 beats per min
  • •Self-report acute viral or bacterial upper or lower respiratory infection at screening
  • •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

研究组 & 干预措施

Low Load Resistance Exercise

Active Comparator

Subjects allocated to Low Load Resistance Exercise will undergo 6 weeks of single-legged low load (25%) resistance exercise. Their contralateral leg will serve as within subject control.

干预措施: Low Load Resistance Exercise (Behavioral)

Low Load Resistance Exercise + BFR

Experimental

Subjects allocated to Low Load Resistance Exercise + BFR will undergo 6 weeks of single-legged low load (25%) resistance exercise plus blood flow restriction. Their contralateral leg will serve as within subject control.

干预措施: Low Load Resistance Exercise + BFR (Behavioral)

结局指标

主要结局

Changes in Mitochondrial Oxidative Capacity

时间窗: Changes from baseline (pre-training) to follow-up (about 48-72 hours post-training).

Changes in mitochondrial oxidative capacity will be measured using near infrared spectroscopy (NIRS).

次要结局

  • Changes in Muscle Strength measured using Isokinetic Dynamometry(Changes from baseline (pre-training) to follow-up (about 48-72 hours post-training))
  • Changes in Muscle Endurance measured using Isokinetic Dynamometry(Changes from baseline (pre-training) to follow-up (about 48-72 hours post-training))
  • Changes in Muscle Mass measured by Dual Energy X-ray Absorptiometry(Changes from baseline (pre-training) to follow-up (about 48-72 hours post-training))

研究者

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

Brian Irving

Assistant Professor

Louisiana State University and A&M College

研究点 (1)

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