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临床试验/IRCT20180114038366N1
IRCT20180114038366N1已完成3 期

Investigation the effect of acupressure on pain, stiffness and physical function of elderly with knee osteoarthritis

Rafsanjan University of Medical Sciences0 个研究点目标入组 96 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
已完成
入组人数
96

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
60 years 至 no limit(—)
性别
All

入选标准

  • Not receiving any supplemental or alternative treatment for osteoarthritis during the last three months
  • Dont have any history of using acupressure for any purpose
  • The absence of any scars, scratches and deformities at points LI 4, SP10, SP9, GB34, ST36, ST34
  • Ability to speak and understand Persian language
  • Having enough power of visual and auditory
  • Do not use anticoagulants or any coagulation disorder
  • Dont have history of surgery associated with the disease (such as replacement and joint repair) on the joint
  • Having osteoarthritis in one or both diapers for at least three months based on the clinical criteria of the American College of Rheumatology
  • BMI below 40.
  • Having a phone line to track
  • Aged over 60 years
  • Having informed consent to participate in the study
  • Not having advanced neuropathy
  • Non-addiction and lack of chronic use of opiates
  • Failure to inject injections into the knee joint or arthroscopy within 30 days prior to intervention
  • Having enough cognitive and functional strength to learn and implement the intervention
  • Lack of history of topical skin lesions and open wounds in acupressure areas, other autoimmune diseases, including lupus erythematosus, have chronic neuropathic conditions such as diabetes.

排除标准

  • Having previous history of acupressure
  • Reduced level of consciousness
  • Patients who do not cooperate for any reason until the end of the intervention
  • Patients who have acute pressure at the points LI4, SP10, SP9, GB34, ST36, ST34 have no feeling of warmth, heaviness, swelling or anesthesia at this point
  • Unwillingness to cooperate with each research unit during the study
  • Injection of housing into the knee joint during the intervention period
  • Those who need to receive housing during the intervention until the second and third assessment of the severity of pain.
  • Lower limb and upper limb
  • Having mental illness during the intervention period

研究者

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