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临床试验/NCT03848741
NCT03848741Unknown不适用

Independent and Combined Effects of Resistance Exercise Training and β-hydroxy β-methylbutyrate Plus Vitamin D on Body Composition and Skeletal Muscle Health

University of Illinois at Urbana-Champaign1 个研究点 分布在 1 个国家目标入组 48 人开始时间: 2019年4月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
48
试验地点
1
主要终点
Skeletal Muscle Function - Knee extensor isokinetic performance

研究概览

简要总结

During middle-age, humans begin to lose muscle mass and strength. With increasing age the deterioration of muscle health is associated with a decline in quality of life and the loss of independence. β-hydroxy β-methylbutyrate (HMB) plus Vitamin D (VitD) have been proposed to increase skeletal muscle mass, contractile function and improve body composition but has yet to be evaluated in middle-aged women. The overall goal of this study is to determine the effects of HMB +VitD supplementation during 12 weeks of resistance exercise training or a non-exercise control on body composition, skeletal muscle size, and skeletal muscle function in middle-aged women.

详细描述

To determine if HMB+VitD supplementation is an effective strategy to help prevent the loss of skeletal muscle size, skeletal muscle function and body composition in middle-aged women, forty eight women (45-60 yrs old) will be recruited to complete a 12-week intervention (n=12 per group; 4 groups). Participants will be randomized to complete a non-exercise control period or a resistance exercise training program. In a double-blinded fashion, participants in the non-exercise or resistance exercise groups will be randomized to consume either placebo or HMB+VitD. Before and after each intervention the investigators will evaluate skeletal muscle size, skeletal muscle function, and body composition.

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
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
45 Years 至 60 Years(Adult)
性别
Female
接受健康志愿者
是

入选标准

  • •Women between 45 and 60 years old
  • •Women with a BMI < 35 kg/m2
  • •Sedentary (< 30 minutes of structured physical activity 3 times per week)
  • •Weight stable for 3 months prior (+/- 5kg)

排除标准

  • •Body mass index > 35 kg/m2
  • •Type 1 or Type 2 diabetes
  • •Uncontrolled hypertension
  • •Active cancer, cancer in remission, or having received treatment for any form of cancer in the previous 5 years
  • •Cardiovascular disease (e.g., peripheral artery disease and peripheral vascular disease)
  • •Uncontrolled thyroid function
  • •Chronic and/or regular consumption of medication known to influence skeletal muscle metabolism
  • •Use of Vitamin D (>2000 IU) or β-hydroxy β-methylbutyrate
  • •Tobacco use
  • •Any condition that limits exercise training (e.g., chronic obstructive pulmonary disease, neuromuscular disorder, moderate or severe cognitive impairment, Alzheimer's disease, vertigo, dizziness)
  • •High alcohol consumption defined as more than 8 drinks per week for women
  • •Unwilling to undergo any study-related procedures
  • •Pregnancy
  • •Abnormal liver or kidney enzymes determined in blood chemistry panel
  • •Bleeding/clotting disorders or blood thinning medications (e.g., warfarin, heparin)

研究组 & 干预措施

Non-exercise control with placebo

Placebo Comparator

Participants will be asked to maintain their normal physical activity and dietary habits during the 12-week intervention. Physical activity, diet, urine and blood samples will be collected every 4 weeks. Each participant will consume 3 placebo capsules (calcium lactate), twice a day with a meal or snack for a total of 6 capsules per day. Placebo capsules match the size, color, weight, and number of capsules per dose compared to the β-hydroxy β-methylbutyrate (HMB) Plus Vitamin D (VitD) capsules.

干预措施: Non-Exercise Control (Behavioral)

Non-exercise control with placebo

Placebo Comparator

Participants will be asked to maintain their normal physical activity and dietary habits during the 12-week intervention. Physical activity, diet, urine and blood samples will be collected every 4 weeks. Each participant will consume 3 placebo capsules (calcium lactate), twice a day with a meal or snack for a total of 6 capsules per day. Placebo capsules match the size, color, weight, and number of capsules per dose compared to the β-hydroxy β-methylbutyrate (HMB) Plus Vitamin D (VitD) capsules.

干预措施: Placebo (Dietary Supplement)

Non-exercise control with HMB+VitD

Experimental

Participants will be asked to maintain their normal physical activity and dietary habits during the 12-week intervention. Physical activity, diet, urine and blood samples will be collected every 4 weeks. Each participant will consume 3 HMB+VitD capsules, twice a day with a meal or snack for a total of 6 capsules per day. Each capsule contains 500 mg calcium HMB and 333.33 IU Vitamin D for a total of 3.0 g HMB and 2000 IU Vitamin D per day.

干预措施: Non-Exercise Control (Behavioral)

Non-exercise control with HMB+VitD

Experimental

Participants will be asked to maintain their normal physical activity and dietary habits during the 12-week intervention. Physical activity, diet, urine and blood samples will be collected every 4 weeks. Each participant will consume 3 HMB+VitD capsules, twice a day with a meal or snack for a total of 6 capsules per day. Each capsule contains 500 mg calcium HMB and 333.33 IU Vitamin D for a total of 3.0 g HMB and 2000 IU Vitamin D per day.

干预措施: HMB+VitD (Dietary Supplement)

Resistance exercise training with placebo

Active Comparator

Participants will complete 12-weeks (3 days per week) of a whole-body progressive resistance exercise training program. Physical activity, diet, urine and blood samples will be collected every 4 weeks. Each participant will consume 3 placebo capsules (calcium lactate), twice a day with a meal or snack for a total of 6 capsules per day. Participants will be asked to take capsules ~30-60 minutes before resistance exercise. Placebo capsules match the size, color, weight, and number of capsules per dose compared to the HMB + VitD capsules.

干预措施: Resistance Exercise Training (Behavioral)

Resistance exercise training with placebo

Active Comparator

Participants will complete 12-weeks (3 days per week) of a whole-body progressive resistance exercise training program. Physical activity, diet, urine and blood samples will be collected every 4 weeks. Each participant will consume 3 placebo capsules (calcium lactate), twice a day with a meal or snack for a total of 6 capsules per day. Participants will be asked to take capsules ~30-60 minutes before resistance exercise. Placebo capsules match the size, color, weight, and number of capsules per dose compared to the HMB + VitD capsules.

干预措施: Placebo (Dietary Supplement)

Resistance exercise training with HMB+VitD

Experimental

Participants will complete 12-weeks (3 days per week) of a whole-body progressive resistance exercise training program. Physical activity, diet, urine and blood samples will be collected every 4 weeks. Each participant will consume 3 HMB+VitD capsules, twice a day with a meal or snack for a total of 6 capsules per day. Participants will be asked to take capsules ~30-60 minutes before resistance exercise. Each capsule contains 500 mg calcium HMB and 333.33 IU Vitamin D for a total of 3.0 g HMB and 2000 IU Vitamin D per day.

干预措施: Resistance Exercise Training (Behavioral)

Resistance exercise training with HMB+VitD

Experimental

Participants will complete 12-weeks (3 days per week) of a whole-body progressive resistance exercise training program. Physical activity, diet, urine and blood samples will be collected every 4 weeks. Each participant will consume 3 HMB+VitD capsules, twice a day with a meal or snack for a total of 6 capsules per day. Participants will be asked to take capsules ~30-60 minutes before resistance exercise. Each capsule contains 500 mg calcium HMB and 333.33 IU Vitamin D for a total of 3.0 g HMB and 2000 IU Vitamin D per day.

干预措施: HMB+VitD (Dietary Supplement)

结局指标

主要结局

Skeletal Muscle Function - Knee extensor isokinetic performance

时间窗: Change from baseline to after the 12 week intervention

Knee extensor isokinetic performance will be assessed by a dynamometer.

Skeletal Muscle Function - Fatigue

时间窗: Change from baseline to after the 12 week intervention

Knee extensor fatigue will be assessed by a dynamometer.

Skeletal Muscle Function - Knee extensor isometric performance

时间窗: Change from baseline to after the 12 week intervention

Knee extensor isometric performance will be assessed by a dynamometer. Muscle strength will also be determined by 1 repetition maximum for leg extension, leg curl and leg press exercises.

Skeletal Muscle Cross Sectional Area

时间窗: Change from baseline to after the 12 week intervention

Skeletal muscle cross sectional area will be assessed via magnetic resonance imaging (MRI).

Body Composition - Percentage

时间窗: Change from baseline to after the 12 week intervention

Fat and fat free percent will be measured using by a dual x-ray absorptiometry (DEXA) scan.

Skeletal Muscle Mitochondrial Respiration

时间窗: Change from baseline to after the 12 week intervention

Mitochondrial respiration will be assessed using high-resolution respirometry in permeabilized muscle fibers.

Body Composition - Mass

时间窗: Change from baseline to after the 12 week intervention

Fat and fat free mass will be measured using by a dual x-ray absorptiometry (DEXA) scan.

Skeletal Muscle Volume

时间窗: Change from baseline to after the 12 week intervention

Skeletal muscle volume will be assessed via magnetic resonance imaging (MRI).

Myofiber Size

时间窗: Change from baseline to after the 12 week intervention

Cross sectional area of muscle fibers will be evaluated with immunohistochemistry.

Skeletal Muscle Mitochondrial Hydrogen Peroxide Emissions

时间窗: Change from baseline to after the 12 week intervention

Mitochondrial hydrogen peroxide emissions will be assessed using high-resolution fluorometry in permeabilized muscle fibers.

次要结局

  • Bone Density(Change from baseline to after the 12 week intervention)

研究者

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

Adam Konopka

Assistant Professor

University of Illinois at Urbana-Champaign

研究点 (1)

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