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
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