Effectiveness of Telerehabilitation in Patients With Osteoarthritis. A Randomized Controlled
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 50
- 试验地点
- 1
- 主要终点
- Rating of Pain
研究概览
简要总结
Randomized controlled study on the effectiveness of Telerehabilitation intervention on subjects with knee osteoarthritis. Subjects will be randomized into two groups. The experimental group perform 3 sessions a week for 4 weeks of TR, the control group 3 sessions a week for 4 weeks of conventional rehabilitation c/o IOR rehabilitation gym. Follow-up at 3 months.
Inclusion criteria
- Subjects must have a diagnosis of rheumatologic disease, osteoarthritis of one or more indications, OARSI criteria.
- Male or Female, aged > 18 years
- Participant is willing and able to provide informed consent for participation in the study.
- Subjects must be able to use an electronic device (pc, tablet, smartphone). Exclusion criteria
1. Participation in another clinical study with any investigational agent within 30 days prior of the study screening.
2. Inability to use an electronic device (pc, tablet, smartphone) 4. Diagnosed with dementia or neurological disease that impairs speech comprehension e Not verbal.
5. Uncontrolled intercurrent illnesses including, without limitation, current infection or active, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia or psychiatric illnesses/social situations that would limit compliance with study requirements, illnesses neurological.
6. Children under the age of 18 8. NPRS value <3 7. BMI >25
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
- 18 Years 至 90 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Subjects must have a diagnosis of rheumatologic disease, osteoarthritis of one or more articulations, OARSI criteria.
- •Male or Female, aged > 18 years
- •Participant is willing and able to provide informed consent for participation in the
- •Subjects must be able to use
排除标准
- •Participation in another clinical study with any investigational agent within 30 days prior
- •of the study screening.
- •Inability to use an electronic device (pc, tablet, smartphone)
- •Diagnosed with dementia or neurological disease that impairs speech comprehension e Not verbal.
- •Uncontrolled intercurrent illnesses including, without limitation, current infection or active, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia or psychiatric illnesses/social situations that would limit compliance with study requirements, illnesses neurological.
- •hildren under the age of 18
- •Numeric Pain Rating Scale(NPRS) value <3
研究组 & 干预措施
Experimental Group
Tele-rehabilitation exercises for the knee joint to reduce pain
干预措施: Exercises for Knee (Other)
Control Group
Exercises in presence for the knee joint to decrease pain
干预措施: Exercises for Knee (Other)
结局指标
主要结局
Rating of Pain
时间窗: one Month
rating of pain in the knee joint with osteoarthritis measured with the nprs pain scale
次要结局
- Quality of life improvement(one month, three month)
- Assessment of knee joint function(one month, three month)