跳至主要内容
临床试验/NCT02485197
NCT02485197已完成不适用

A Pilot Study Investigating Differences in Muscle Metabolic Function in Individuals Aged 65-75 Years With Different Vitamin D Status Before and After 7-days of Aerobic Training

David Travis Thomas1 个研究点 分布在 1 个国家目标入组 7 人开始时间: 2013年3月1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
发起方
入组人数
7
试验地点
1
主要终点
Muscle VO2 consumption

研究概览

简要总结

This is a small pilot aerobic training trial designed to examine differences between normal-high and low vitamin D levels and 7-days of aerobic training on local VO2 measured by non-invasive Hybrid Diffuse Optical Spectroscopy.

研究设计

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

入排标准

年龄范围
65 Years 至 75 Years(Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •65-75 years of age

排除标准

  • •Currently have or have a history of cardiovascular or pulmonary disease that would preclude the involvement in the performance of exercise.
  • •Uncontrolled diabetes or hypertension.
  • •History of neurological conditions related to spinal derangement, disk disease, peripheral neuropathies, tremor and rigidity
  • •History of leg/hip trauma, inflammation, infection rhabdomyolysis, or leg surgery in the past 3 months
  • •Have a diagnosis of osteoporosis (as determined by DXA)
  • •Participated in a resistance or aerobic training program in the last 3 months
  • •Engage in more than 1 hr/week of vigorous activity
  • •Body mass index >29
  • •On hormone replacement therapy

研究组 & 干预措施

Low 25(OH)D

Other

We will recruit individuals with low 25(OH)D (<30ng/mL).

干预措施: 7 continuous days of aerobic training (Other)

High 25(OH)D

Other

We will recruit individuals with higher 25(OH)D (at least 20ng/mL units higher then that of the "low 25(OH)D group).

干预措施: 7 continuous days of aerobic training (Other)

结局指标

主要结局

Muscle VO2 consumption

时间窗: Up to 3 months

The objective is to examine the difference in gastrocnemius VO2 consumption in individuals that either have normal-high or low 25(OH)D and are undergoing 7-days of a treadmill training program.

次要结局

未报告次要终点

研究者

发起方
David Travis Thomas
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

David Travis Thomas

Ph.D., RD, CSSD, CSCS

University of Kentucky

研究点 (1)

Loading locations...

相似试验