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临床试验/NCT00421408
NCT00421408已完成1 期

Impact of a Protein Supplement on Bone Mass in Older Men and Women

Yale University2 个研究点 分布在 1 个国家目标入组 208 人开始时间: 2007年2月1日最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
已完成
入组人数
208
试验地点
2
主要终点
Change in Spine Bone Mineral Density Measured by Quantitative Computed Tomography (QCT) Compared to Baseline

研究概览

简要总结

Women and men consuming a low protein diet may be at risk for bone loss. The purpose of this study is to determine whether a daily protein supplement will improve bone health among healthy older adults.

详细描述

Dietary protein plays an important role in maintaining balanced calcium levels in the body. Protein's impact on skeletal health remains unclear. It is well accepted that increasing dietary protein results in greater excretion of calcium through urine. The excreted calcium is thought to come in part from bone, which would suggest a negative effect on bone health. However, recent studies have found that higher protein intake is, in fact, associated with higher bone mineral density and lower rates of bone loss. The purpose of this study is to determine if a daily protein supplement will improve bone health and hormonal measures of bone metabolism among healthy older men and women who consume low-to-normal levels of dietary protein.

This study will last 18 months. For the duration of the study, participants will be randomly assigned to receive either a 40-gram protein supplement or placebo daily. There will be a total of nine study visits that will occur at screening, study entry, Month 1.5, and every three months thereafter. Dietary records, nutritional counseling, glucose finger stick tests, and questionnaires related to falls, physical activity, habits, and study satisfaction will occur at all study visits. Blood and urine collection, functional testing, and bone mineral density (BMD) testing will occur at selected visits. At Months 0 and 18, half of the participants will undergo a quantitative computed tomography (CT) scan to determine bone mineral density.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

年龄范围
60 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Willing to travel to one of the study sites
  • •Women age 60 years or greater, men age 70 years or greater
  • •Dietary protein intake level between 0.6 g/kg and 1.0 g/kg at baseline

排除标准

  • •Active Paget's disease
  • •Primary hyperparathyroidism or unexplained hypercalcemia
  • •Untreated hyperthyroidism or hyperthyroidism that has resulted from medical treatment
  • •Diabetes mellitus type 1
  • •Cancer diagnosis for solid malignancies (e.g., cancer of the colon, breast,prostate, lungs, lymphocytes) within the 18 months prior to study entry
  • •Long-term use of chemotherapeutic drugs, aromatase inhibitors, or tamoxifen
  • •Active treatment for leukemia or multiple myeloma
  • •Active inflammatory bowel disease
  • •Life expectancy of less than 2 years
  • •Current and ongoing use of methotrexate, phenytoin, phenobarbital, or inhaled corticosteroids at a dose of greater than 800 mcg/day
  • •Use of raloxifene, estrogen, androgen, progesterone, soy isoflavones, oral glucocorticoids, or herbal supplements with estrogenic activity OR a change in dosage of thyroid medications within the 1 year prior to study entry if unwilling to avoid such agents during the duration of the study
  • •Current use of antiresorptive agents (e.g., calcitonin or bisphosphonates). More information about this criterion can be found in the protocol.
  • •serum creatinine greater than 1.2 mg/dl
  • •History of chronic liver disease or evidence of liver disease at screening
  • •Bilateral hip replacement
  • •women who have a bone mineral density T-score < -2.5 at either the hip or spine unless they have decided to decline treatment with conventional anti-osteoporotic medications
  • •Body mass index (BMI) greater than 32 or less than 19
  • •Use of proton-pump inhibitors taken twice daily
  • •Fasting glucose level greater than 110 mg/dl
  • •Serum albumin level less than 3.0 mg/dl
  • •Kidney stones or history of kidney stones within the 3 years prior to study entry

研究组 & 干预措施

Protein powder

Experimental

Participants will receive a protein supplement daily (40 g whey protein supplement).

干预措施: Whey protein supplement (Dietary Supplement)

Placebo carbohydrate

Placebo Comparator

Participants will receive a placebo supplement daily (40 g maltodextrin).

干预措施: Placebo (Dietary Supplement)

结局指标

主要结局

Change in Spine Bone Mineral Density Measured by Quantitative Computed Tomography (QCT) Compared to Baseline

时间窗: Measured at baseline and 18 months

There is no normative data for quantitative computed tomography it is based on local experience.

Spine Bone Mineral Density Measured by Quantitative Computed Tomography (QCT) at Baseline

时间窗: Measured at 0 months

There is no normative data for quantitative computed tomography it is based on local experience.

Anterior-posterior Spine Bone Mineral Density Measured by Dual Energy X-ray Absorptiometry (DXA) at 18 Months

时间窗: Measured at 18 months

There is no absolute normative range for bone mineral density. Population norms have been established for specific races and men and women for the hip based on data collected by National Health Examination Nutrition Surveys (NHANES) and for the spine based largely on data collected by individual manufacturers. Values within 1 standard deviation of the population mean are generally considered normal. Values below 1 standard deviation from the population mean are generally considered to reflect reduced bone mass.

Change in Anterior-posterior Spine Bone Mass Density Measured by Dual Energy X-ray Absorptiometry (DXA) Compared to Baseline

时间窗: Measured at baseline and 18 months

There is no absolute normative range for bone mineral density. Population norms have been established for specific races and men and women for the hip based on data collected by National Health Examination Nutrition Surveys (NHANES) and for the spine based largely on data collected by individual manufacturers. Values within 1 standard deviation of the population mean are generally considered normal. Values below 1 standard deviation from the population mean are generally considered to reflect reduced bone mass.

Anterior-posterior Spine Bone Mineral Density Measured by Dual Energy X-ray Absorptiometry (DXA) at Baseline

时间窗: Measured at 0 months

There is no absolute normative range for bone mineral density. Population norms have been established for specific races and men and women for the hip based on data collected by National Health Examination Nutrition Surveys (NHANES) and for the spine based largely on data collected by individual manufacturers. Values within 1 standard deviation of the population mean are generally considered normal. Values below 1 standard deviation from the population mean are generally considered to reflect reduced bone mass.

Anterior-posterior Spine Bone Mineral Density Measured by Dual Energy X-ray Absorptiometry (DXA) at 9 Months

时间窗: Measured at 9 months

There is no absolute normative range for bone mineral density. Population norms have been established for specific races and men and women for the hip based on data collected by National Health Examination Nutrition Surveys (NHANES) and for the spine based largely on data collected by individual manufacturers. Values within 1 standard deviation of the population mean are generally considered normal. Values below 1 standard deviation from the population mean are generally considered to reflect reduced bone mass.

Spine Bone Mineral Density Measured by Quantitative Computed Tomography (QCT) at 18 Months

时间窗: Measured at 18 months

There is no normative data for quantitative computed tomography it is based on local experience.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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