跳至主要内容
临床试验/NCT02608749
NCT02608749已完成不适用

Osteoporosis and Fall Prevention High Risk Population Intervention and Follow up in the Metropolitan Area

National Taiwan University Hospital2 个研究点 分布在 1 个国家目标入组 151 人开始时间: 2014年5月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
151
试验地点
2
主要终点
Lower extremity extensor power measured by isokinetic resistance equipment

研究概览

简要总结

BACKGROUND: The deterioration of musculoskeletal system imposes significant impact on physical activity in older adults.

METHODS: This was a randomized, parallel-group, prospective study. All participants received education program including home-based exercise. The IC group consisted of different modalities of exercise while the LEE group performed machine-based exercise. Body composition, muscle strength, and physical performance were measured at their baseline and 3 months follow-up.

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
None

入排标准

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

入选标准

  • older than 50 years of age
  • high risk as defined from one of the following criteria
  • score>=1 on one minute osteoporosis risk questionnaire
  • 10 year predicted fracture risk >=20% for major osteoporosis fracture or >=3% for hip fracture from FRAX
  • fall>=2 times in pass 1 year
  • having a bone mineral density test within one year period
  • having the capability to understand the study and complete the study interventions
  • willing to participate for the intervention and study follow ups

排除标准

  • If patients were unable to meet at least the above inclusion criteria.

研究组 & 干预措施

HC

Experimental

Home care (HC)

干预措施: Home care (HC) (Behavioral)

IC

Experimental

Integrated care (IC)

干预措施: Integrated care (IC) (Behavioral)

LEE

Experimental

Lower extremity exercise (LEE)

干预措施: Lower extremity exercise (LEE) (Behavioral)

结局指标

主要结局

Lower extremity extensor power measured by isokinetic resistance equipment

时间窗: 12 weeks

Lower extremity extensor power is measured by isokinetic resistance equipment by a trained research assistant with standardized protocol

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)

Loading locations...

相似试验