Progressive Resistance Exercise in Rheumatoid Arthritis
Progressive Resistance Exercise in Rheumatoid Arthritis Patients: a Randomized Controlled Trial
研究概览
研究类型
注册 (实际的)
阶段
- 第四阶段
联系人和位置
学习地点
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SP
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Sao Paulo、SP、巴西、04023-900
- Universidade Federal de Sao Paulo
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参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- Rheumatoid arthritis according to American College of Rheumatology 2010
- Both genders
- Age between 18 and 65 years
- Functional class I, II and III
- Stable medication within the three months preceding the study
- Haven't done any kind of regular exercise (two or more times per Week) for at least three months before study start
- Have agreed to participate in the study and signed an informed consent form.
Exclusion Criteria:
- Participating in another type of study
- Have difficulty understanding the evaluation tools with fibromyalgia
- Joint deformities that make impossible do the exercises
- Other musculoskeletal diseases
- Other diseases that contraindicate exercises.
学习计划
研究是如何设计的？
设计细节
- 主要用途：治疗
- 分配：随机化
- 介入模型：并行分配
- 屏蔽：单身的
武器和干预
参与者组/臂 |
干预/治疗 |
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有源比较器：Control group
Patient remain with their usual clinical treatment.
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其他名称：
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实验性的：Experimental group
Patients in experimental group participated in a 12-week progressive resistance training using a maximum repetition exercise in which patients performed 1 Maximum Repetition with the maximum bearable weight. Once the 1 Maximum Repetitionwas determined, training was divided into the following regimen: 2 series of 8 repetitions, the first with 50% and the second with 70% of 1 Maximum Repetition. The exercises were knee extension and flexion and hip abduction and adduction, elbow extension and flexion, wrist extension and flexion and shoulder abduction and adduction and spine extension and flexion all performed in machines. The 1 Maximum Repetition load was reevaluated every 6 weeks. Patient remain with their usual clinical treatment. |
其他名称：
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研究衡量的是什么？
主要结果指标
结果测量 |
大体时间 |
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Change in pain - Visual analogue scale
大体时间：baseline, 6, 12 and 24 weeks
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baseline, 6, 12 and 24 weeks
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次要结果测量
结果测量 |
大体时间 |
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Change in function capacity - Health Assessment questionaire
大体时间：Baseline, after 6, 12 and 24 weeks
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Baseline, after 6, 12 and 24 weeks
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Change in quality of life - Short form 36
大体时间：baseline, after 6, 12 and 24 weeks
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baseline, after 6, 12 and 24 weeks
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Change in strength - 1 maximum repetition
大体时间：baseline, after 6, 12 and 24 weeks
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baseline, after 6, 12 and 24 weeks
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合作者和调查者
研究记录日期
研究主要日期
学习开始
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (估计)
上次提交的符合 QC 标准的更新
最后验证
更多信息
此信息直接从 clinicaltrials.gov 网站检索，没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求，请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改，我们的网站上也会自动更新.
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