ISRCTN27865285已完成不适用
Study of the clinical benefit and quality of life perception in patients with osteoarthritis of the hip and the knee. Evaluation based on a proactive follow-up intervention made by primary care physicians. Experimental open, randomized and controlled study.
Spanish Society of Family Medicine and Community (Sociedad Española de Medicina de Familia y Comunitaria [SEMFYC]) (Spain)0 个研究点目标入组 1,925 人开始时间: 2010年2月19日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 1,925
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
- 性别
- All
入选标准
- •Physicians:
- •1. Belong to reselected Primary Care health centre
- •2. Have a daily clinical activity
- •3. Able to demonstrate a permanency up to 9 months in a clinical job
- •4. Commitment to follow all study criteria and recommendations
- •1. Known diagnosis of hip and/or knee osteoarthritis fulfilling American College of Rheumatology (ACR) criteria.
- •2. Selected by physician (study subject) and gives informed consent to participate in this trial.
排除标准
- •Physicians:
- •1. Unable to ensure job stability at Primary Care health centre over 9 months
- •2. Does not accept study criteria and recommendations
- •3. Already involved in improvement effort programs regarding clinical support for patients affected by joint disease
- •1. Clinical antecedents of actual arthritic disease with prosthesis implanted
- •2. Arthritic disease involving exclusively or predominantly the spine (all locations) or upper limbs
- •3. Severe concomitant pathology with a short term life expectancy
- •4. Existence of non-arthritic rheumatic condition (fibromyalgia, rheumatoid arthritis, psoriasis, collagen diseases)
- •5. Psychological or sensorial impairment that prevents study participation
- •6. Existence of any absolute contraindication for anti-arthritic medications (Non-Steroidal Anti-Inflammatory Drugs [NSAIDs], etc.)
- •7. Does not wish to participate
- •8. Potential surgical intervention (next 6 months)
- •9. Additionally, any patients considered by his/her physician to be clinically inappropriate for participation and clinical data collection in this study
研究者
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