DRKS00009257已完成未知
Effectiveness and efficiency of a supervised strength-machine based hip and knee training for patients with hip or knee osteoarthritis: A controlled study in the context of health service research. - SM-HKT
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 143
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Non-randomized controlled study
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 one（—）
- 性别
- All
入选标准
- •Lifetime prevalence of hip and/or knee OA diagnosed by a medical practitioner
- •Insurant of the insurance company offering the exercise program
- •Physical and mental ability to participate in the interventional program
排除标准
- •- Hypertension Stage 2-3: reread systolic blood pressure >160 prior maximum strength testing, reread diastolic blood pressure >100 prior maximum strength testing (Intervention group only)
- •- Significant established osteoporosis requiring treatment, previous spontaneous or low impact fracture
- •- Co-morbidities leading to major impairments in everyday life and representing contra-indications for physical activities
- •- Artificial joint replacement at the knee and/or hip joint within the last 6 months
- •- Surgery at the lower extremity within the last 3 months
- •- Regular use of gait aids
- •- Self-reported acute illness on t0
- •- Insufficient German language ability for self-administered questionnaires (IG)
- •- Current employment in the health care insurance
- •Exclusion criteria for primary data analysis only:
- •- < 15 points on the WOMAC Index, subscale pain (0-100) and < 15 points on the WOMAC Index, subscale physical functioning
- •In case of a previous artificial joint replacement at the hip and/or knee joint:
- •- Acute joint inflammation
- •- Instable anchoring of the artificial joint
- •- Radiologic signs of implant loosening
- •- Pain at rest or with activity due to artificial joint replacement at the knee and/or hip joint
- •- Luxation as an adverse event of artificial hip replacement
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