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临床试验/NCT01164670
NCT01164670已完成不适用

Evaluation of the Reproducibility of Jumping Mechanography in Older Adults and Comparison With Current Functional Assessment Tools

University of Wisconsin, Madison1 个研究点 分布在 1 个国家目标入组 96 人开始时间: 2010年5月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
96
试验地点
1

研究概览

简要总结

Sarcopenia, the age-related decline in muscle mass and function (widely recognized as "frailty"), is increasingly being appreciated, primarily in the research environment. Interventions to prevent or treat sarcopenia can be anticipated to reduce falls, fractures and thereby to facilitate independence and improve quality of life for older adults. Unfortunately, there is no current consensus definition of sarcopenia, thereby impeding clinical recognition and treatment. It has been advocated that low appendicular (arm and leg) lean mass, as measured by DXA, be utilized as a clinical diagnostic tool to define sarcopenia. While such an approach is possible, however, muscle strength loss is more rapid than mass loss, indicating deterioration of muscle "quality." Muscle quality may be affected by changes at the neuromuscular, cellular or subcellular levels; parameters not detected by measuring mass alone. Clearly, tools evaluating muscle performance, not simply mass, are needed to optimally identify, and subsequently monitor, treatment of older adults with sarcopenia. While current tests of muscle power/function (e.g., chair-rising, self-selected gait velocity, etc.) do correlate with functional limitation in older adults, these existing tests have limitations in that they cannot be performed in all people, may have "yes/no" results rather than a continuous scale and may not be highly precise. Thus, improved muscle function assessment tools are needed, both clinically and in research venues. Jumping mechanography is very likely one such methodology.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • •Ambulatory, community dwelling men and women age ≥ 70 years
  • •Able and willing to sign informed consent
  • •Able to stand without assistance

排除标准

  • •Abnormalities on screening laboratory assessment deemed to be clinically significant by the study investigators
  • •History of myocardial infarction within the prior six months or ongoing angina
  • •History of injury or surgery within the prior six months which limits the ability to ambulate
  • •History of severe end-organ disease, e.g., cardiovascular, hepatic, hematologic, pulmonary, etc., which might limit the ability to complete this study
  • •History of malignancy with metastasis to the musculoskeletal system
  • •Neuromuscular disease impairing balance to the degree of not being able to stand without assistance
  • •BMD T-score of less than -3.5 at any measured site and a prior hip or vertebral fracture

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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