NL-OMON33836
招募中
不适用
STABILO: a randomised controlled trial of knee joint stabilisation therapy in osteoarthritis of the knee - STABILO
概览
- 阶段
- 不适用
- 干预措施
- 未指定
- 疾病 / 适应症
- arthrosis
- 发起方
- Vrije Universiteit Medisch Centrum
- 入组人数
- 120
- 状态
- 招募中
- 最后更新
- 去年
概览
简要总结
暂无简介。
研究者
入排标准
入选标准
- •All potential participants\* eligibility will first be assessed by a physiatrist, using the following inclusion criteria:
- •\- diagnosis of knee OA according to the clinical ACR criteria, i.e.: knee pain and at least three of the following six: age \> 50 years, morning stiffness \<30 minutes, crepitus, bony tenderness, bony enlargement and no palpable warmth.
- •\- Age between 40 and 75 years
- •\- Sufficient control of the Dutch language;Patients meeting these initial inclusion criteria will then be screened for symptoms of knee joint instability by a physical therapist. Patients are eligible for inclusion in the trial if they meet at least one of the following three criteria:
- •1\. self\-reported instability of the knee joint affecting daily functioning, as assessed with Irrgang\*s knee stability questionnaire. A self\-reported knee instability rating of 1 (\*the symptom affects my activity slightly\*) or worse is regarded to reflect knee instability affecting daily functioning
- •2\. bodyweight\-adjusted isokinetic quadriceps strength of 0\.8 Nm/kg or less for men or 0\.55 Nm/kg or less for women, in combination with a knee joint proprioception score of 4\.3° or higher, as established with the instrumented knee proprioception test (9;28\)
- •3\. bodyweight\-adjusted isokinetic quadriceps strength of 0\.8 Nm/kg or less for men or 0\.55 Nm/kg or less for women, in combination with a knee joint laxity score of 4\.6° or higher for men or 7\.7° or higher for women, as established with the instrumented knee laxity test (8;27\)}
排除标准
- •Co\-morbidity which affects functional ability
结局指标
主要结局
未指定
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