Treatment for Osgood Schlatter Patients With a Physiotherapy Program "TrOPhy-Study"
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 36
- 试验地点
- 2
- 主要终点
- change in Knee and Osteoarthritis Outcome Score for Children (KOOS-Child-Questionnaire Score)
研究概览
简要总结
This study is to compare the effect of a physiotherapy program to usual care treatment in patients with Osgood Schlatter disease (OSD). Patients will be randomly assigned into two groups. Group 1 will receive the physiotherapy program with myofascial massage, while group 2 (usual care group USC) will receive usual care treatment.
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
- Single (Outcomes Assessor)
入排标准
- 年龄范围
- 10 Years 至 17 Years（Child）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Uni- or bilateral OSD
- •ability to follow instructions
- •sufficient knowledge of German
- •availability: can participate in two exercise sessions per week for a period of 8 weeks
排除标准
- •any history of knee surgery
- •medication intake affecting the knee
- •unstable fractures
- •neurological disorders
- •systematic diseases
- •already in physiotherapeutic treatment because of the knee
- •not possible to do any physiotherapy sessions at the Universitäts-Kinderspital Basel (UKBB)
结局指标
主要结局
change in Knee and Osteoarthritis Outcome Score for Children (KOOS-Child-Questionnaire Score)
时间窗: at baseline and 8 weeks after baseline
KOOS-Child is a patient-reported outcome measure employing five-item Likert scales. KOOS-Child covers 5 dimensions (subscales): Pain, Symptoms (titled "Knee problems" in the KOOS-Child), Difficulty during daily activities (ADL), Function in sport and play (Sports/Play) and knee-related Quality of Life (QOL). 0-100 scale, with zero representing extreme knee problems and 100 representing no knee problems
次要结局
- Change in Y Balance Test (Lower Quarter)(at baseline and 8 weeks after baseline)
- Change in Range of motion (ROM) of knee(at baseline and 8 weeks after baseline)
- Time of return to sport activity (in days)(within 8 weeks after baseline)
- Change in Knee pain assessed by Visual Analogue Scale (VAS)(at baseline and 8 weeks after baseline)