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临床试验/DRKS00009251
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Effectiveness and efficiency of a group-based hip and knee training in combination with a structured home-exercise program for patients with hip or knee osteoarthritis: A controlled study in the context of health service research. - HKT

AOK Baden-Württemberg0 个研究点目标入组 3,470 人开始时间: 2015年9月10日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
3,470

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

  • •- 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

研究者

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