Investigation of the Effects of Physiotherapy on Pain, Physical Function and Quality of Life in Patients With PRP Applied Knee Osteoarthritis
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 26
- 试验地点
- 1
- 主要终点
- Change from Baseline Pain Level at Six Week
研究概览
简要总结
This study evaluates effects of PRP and physiotherapy on pain, physical function and quality of life in patients with knee osteoarthritis.
详细描述
PRP has been reported to have a low to moderate level of evidence in patients with knee osteoarthritis (OA) in reducing pain and improving function. Similarly, in individuals with knee osteoarthritis, exercise has been reported to be effective in reducing the pain and improving physical function of the knee OA patient in the short term, and may be even more effective with individual exercise programs. However, there is no study examining the effect of PRP and exercise together. PRP and exercise can be more effective together. The aim of our study was to investigate the effects of physiotherapy on pain, physical function and quality of life in patients with knee OA who underwent PRP injection.
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
- 45 Years 至 65 Years（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Grade 2-3 according to Kellgren Lawrence osteoarthritis classification,
- •Patients with knee osteoarthritis who underwent PRP injection at least three days ago,
- •Being volunteer
排除标准
- •Any intra-articular application and / or physiotherapy and rehabilitation in the last 6 months,
- •Have any other orthopedic problems involving the lower extremities
- •Having cognitive problems,
- •Having additional neurological, rheumatologic and / or oncological problems
研究组 & 干预措施
Physiotherapy
Exercise intervention will be applied to this arm.
干预措施: Exercise (Other)
Control
No intervention will be made to this arm, only evaluations will be made.
结局指标
主要结局
Change from Baseline Pain Level at Six Week
时间窗: At baseline, six week
Pain change will be measured throughout Study and Follow-up with Visual Analog Scale. This scale is a 100 millimeter line drawn horizontally on an A4 sheet of paper. The left end of the line shows "no pain at all", the right end shows "my pain is as bad as it could be", while the remaining part shows the intermediate values. So minimum score was 0, and maximum score was 100. The patient is asked to mark the severity of the pain on the chart. Validity and reliability were made. The minimal clinical significance difference in chronic low back pain was 20 millimeters.
次要结局
未报告次要终点
研究者
Sibel Bozgeyik
PT, PhD(c)
Hacettepe University