NL-OMON33836招募中不适用
STABILO: a randomised controlled trial of knee joint stabilisation therapy in osteoarthritis of the knee - STABILO
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 120
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 99（—）
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
研究者
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