NCT00327275已完成不适用
The Strength Training and Remicade Study
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 35
- 试验地点
- 2
- 主要终点
- Strength
研究概览
简要总结
To assess the effects of a 16-week individualized, intensive strength training program in patients with rheumatoid arthritis. Primary and secondary outcomes include: strength and body composition, function, disease activity, pain, quality of life.
We hypothesized that improvements would be seen in all of the above outcomes.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Single Group
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Males and females with RA
- •Over 18 years of age
- •ACR Functional Class I and II
- •Taking Remicade >4 months
排除标准
- •Presence of comorbid conditions contraindicated to exercise, including, but not limited to:
- •heart disease
- •severe osteoporosis: (if >50 years): T score < -3.0 for hip or spine excluded; T score <-2.5 for hip or spine w/o current treatment)
- •(all potential subjects) previous non-traumatic fractures
- •uncontrolled BP
- •Regular use of assistive walking device which would interfere with ability to lift weights
- •Currently or within the last 3 months participating in aerobic exercise > 150 minutes a week
- •Currently or within the last 3 months participating in any regular strength training activities
- •Presence of neurological impairment that directly limits ability to perform exercise
- •Participation in concurrent exercise study
- •Any reason for which the investigator deems it would not be in the patient's best interest to continue in the study
- •Plans to move away from site within next 1 year
结局指标
主要结局
Strength
Body Composition
Function
Pain
次要结局
- Disease Activity
- Fatigue
- Quality of Life
研究者
研究点 (2)
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