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临床试验/NCT00434915
NCT00434915已完成不适用

Does DHEA Enhance the Effects of Exercise in Postmenopausal Women?

Mayo Clinic2 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2003年4月最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
Mayo Clinic
入组人数
32
试验地点
2
主要终点
quality of life

研究概览

简要总结

Dehydroepiandrostrone (DHEA) and its sulfated ester (DHEAS) are high circulating weak androgens which have been associated with conditions that accompany age-related decline such as sarcopenia, hyperinsulinemia, osteopenia, and cardiovascular disease. The decline in DHEA with age is particularly marked in postmenopausal women. Exercise has always been advocated in women; benefit has been demonstrated inmuscle, bone and lipid physiology, as well as perception of energy and sense of well-being. This study aims to explore the combined effect of both DHEA and exercise in postmenopausal women, age range 55-75 years old. Subjects will receive DHEA (50mg/day) or placebo for a 12-week period. At the beginning and conclusion of the study patients will undergo testing for muscle strength, body composition, VO2 max, insulin sensitivity, muscle biopsy with mitochondria enzyme measurements, and psychological analysis. Blood samples pre and post intervention will also be obtained and the level of selected anabolic markers, lipids, and androgenic and sex steroid levels will be assessed. For the twelve-week period, both placebo and DHEA treated participants will be involved in a resistance and aerobic exercise program coordinated through the GCRC and the Dan Abraham Healthy Living Center. Several correlations have been established with respect to exogenous DHEA administration in postmenopausal women. None have evaluated oral DHEA therapy in the setting resistance and aerobic exercise, key therapies advocated in postmenopausal women. As a plausible anabolic hormone DHEA is hypothesized to accentuate the effects of exercise as has been shown for testosterone. This study, as a randomized double-blind placebo controlled trial, will investigate the effects, if any, of a regimented exercise program and DHEA supplementation in postmenopausal women, specifically for evidence of enhancement of exercise effect by oral supplementation with DHEA in attenuating age-related decline

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Double

入排标准

年龄范围
55 Years 至 75 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Subjects will be postmenopausal women between the ages of 60 and 75 years old.
  • Women with levels of DHEA less than 110 mg will be selected.

排除标准

  • Individuals with history or biochemical evidence of liver disease, cardiovascular disease (other than controlled hypertension); polycythemia, cerebrovascular disorders, or disorder of glucose metabolism with fasting hyperglycemia or hypoglycemia will be excluded.
  • Use of psycotropic drugs within six months prior to enrollment
  • History of severe depression or psychotic disorder
  • Professional athletes or BMI greater than 30kg/m2
  • Anyone who has been in a regular (greater than twice/weekly) exercise program for more than 2 months prior to the study
  • Severe rheumatologic condition with chronic pain not well controlled.
  • Use of DHEA, estrogen, progesterone, testosterone, corticosteroid products up to six months prior to study

结局指标

主要结局

quality of life

glucose and insulin metabolism

body composition

physical performance (VO2 peak, muscle strength as measured by chest press, double knee extension, and isokinetic knee extension

muscle protein synthesis

次要结局

未报告次要终点

研究者

发起方
Mayo Clinic
申办方类型
Other

研究点 (2)

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