跳至主要内容
临床试验/NL-OMON29122
NL-OMON29122尚未招募不适用

europrotective Effects of Exercise in People with Progressive Multiple Sclerosis: a phase II trial.

Amsterdam UMC, location VUmc0 个研究点目标入组 60 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
60

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

入选标准

  • PMS diagnosis defined as: ‘definite diagnosis of MS according to the 2017 McDonald Criteria with gradual progression of neurological impairments according to the Lublin criteria 2013.’
  • EDSS Scale 3.5 – 6
  • Able to participate in the exercise programs, i.e. no contra-indications for training according to the guidelines of the American college of Sports Medicine.
  • oNo history of heart problems
  • oNo symptoms that might indicate heart problems
  • oNo other major health issues
  • Age between 18 and 60 years old
  • Able to understand therapists instructions
  • Fulfilling the safety criteria for magnetic resonance (MR) assessment
  • oNo metal inside the body
  • oNot claustrophobic
  • oNo pregnancy

排除标准

  • Diagnosed with PPMS
  • Relapse within 3 months of baseline visit
  • Severe comorbidity (Cumulative Illness Rating Scale (CIRS) = 3 on 1 or more organ systems).
  • Initiation of Fampridine within 6 months of baseline visit.
  • Depression, Hospital Anxiety and Depression Scale (HADS) score, depression subscale =11 (i.e. indicative of clinical anxiety disorder or clinical depression)
  • Other neurological- and/or musculoskeletal disorders
  • Already participating in a (guided) high intensity exercise training
  • Participating in another intervention study
  • Pregnancy, given birth previous 6 months, or active pregnancy wish.

研究者

发起方
Amsterdam UMC, location VUmc

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Exercise in Progressive Multiple Sclerosis | 临床试验