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临床试验/NCT02855801
NCT02855801终止不适用

Exercise Training in Patients With Rheumatoid Arthritis and Cryotherapy: Feasibility Study

Centre Hospitalier Universitaire de Besancon2 个研究点 分布在 1 个国家目标入组 8 人开始时间: 2013年6月最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
8
试验地点
2
主要终点
plasma concentration of C-reactive protein

研究概览

简要总结

The main objective of this project is to study, in patients with rheumatoid arthritis, the effects of an intermittent type exercise associated with cryotherapy on the level of inflammation during its recovery.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Investigator)

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Men and women >18 years old, < 80 years old
  • Signature of informed consent for participation
  • Affiliation to a social security scheme or French beneficiary of such a regime.
  • confirmed rheumatoid arthritis and monitoring by the rheumatology department of the University Hospital of Besancon.
  • If there is a corticosteroid therapy, it must be stable for at least 1 month and less than or equal to 10 mg of prednisone equivalent per day
  • Clinical and biological activity will be moderate (ie not in remission and not severe based on Disease Activity Score 28 joints - DAS 28 - to be between 2 and 6
  • Patients could be treated with DMARDs (Disease-Modifying Drugs).

排除标准

  • Patient under guardianship, curatorship, under judicial protection, major incapable
  • Patients whose body mass index (BMI) greater than 30,
  • Pathology incompatible with the completion of a cycle ergometer exercise (heart, vascular, respiratory, orthopedic ...)
  • Change in DAS28 greater than 1.2 in the previous 3 months Inclusion
  • A patient with a DAS28 > 6
  • about the cold: Raynaud's syndrome, cold known allergy, sickle cell anemia, cryoglobulinemia, uncontrolled hypertension
  • Patient unable to follow protocol because of cognitive, psychiatric or language difficulties.
  • Inability to follow protocol for causes related to health problems (unrelated Rheumatoid Arthritis) or socio-professional.

结局指标

主要结局

plasma concentration of C-reactive protein

时间窗: 48 hours after the end of the exercise

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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