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临床试验/PACTR202403516079512
PACTR202403516079512尚未招募3 期

Treatment of Progressive Multiple Sclerosis-related Cognitive Impairment, Fatigue, and Depression Using Repetitive Transcranial Magnetic Stimulation

Science Technology and Innovation Funding Authority0 个研究点目标入组 60 人开始时间: 2024年1月14日最近更新:
适应症

试验速览

阶段
3 期
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

年龄范围
19 Year(s) 至 44 Year(s)(—)
性别
All

入选标准

  • Definite MS patients according to 2017 revisions of the McDonald criteria.
  • -Progressive types of MS: Patient must fulfill diagnostic criteria of either: Secondary progressive MS (SPMS) or Primary progressive MS (PPMS)
  • -Free of clinical relapses for at least 3 months prior to inclusion.
  • -Free of steroid treatment for at least 6 weeks prior to inclusion.
  • -No change in their medications, whether disease modifying treatment or symptomatic therapy for at least 3 months if applicable.
  • -EDSS score below 6 points and stable over the past 3 months.
  • -A score of <34 on Symbol Digit Modalities Test, a score of = 12 on the Beck Depression Inventory (Beck et al., 1961), a score of = 38 on the Modified Fatigue Impact Scale.
  • -Level of education: at least can read and write.
  • -Written informed consent from the participants

排除标准

  • -Conditions that could affect the participants’ level of cognition, fatigue, or depression, including; pregnancy, history of substance use disorder, history of significant neurological disorder other than MS, psychiatric, endocrinological, hepatic, renal, collagen, or other systemic comorbidities that could affect these symptoms.
  • -Contraindication to TMS: history of seizures, skull bone defects, metal fragments in the head, implanted metallic devices such as cardiac pacemakers, cochlear implants, medical pumps…, etc.
  • -Illiterate patients.

研究者

发起方
Science Technology and Innovation Funding Authority

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