跳至主要内容
临床试验/CTRI/2019/10/021800
CTRI/2019/10/021800进行中(未招募)2 期

An Open Label, Prospective, Randomised, Comparative, Two Arm Clinical Study to Evaluate the Effectiveness of Gaming Platform ââ?¬â?? COSMA Software from Cerebrum Matter Ltd. in Adults with Mild NeuroCognitive Impairment, Vascular Dementia and/or Dementia Associated with Alzheimerââ?¬â?¢s Disease.

Cerebrum Matter Limited0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
进行中(未招募)
发起方

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

  • 1.Verified neurological evaluation and diagnosis of Mild NeuroCognitive Impairment, Vascular Dementia and/or Dementia associated with Alzheimerââ?¬•s Disease
  • 2.Neurocognitive evaluation with Functional Assessment Staging Test : Stage 3 to Stage 5
  • 3.Male and female adults less than 65 years of age
  • 4.Subjects who are classified as right handed
  • 5.Subjects who can read and write Tamil and/or English
  • 6.Subjects who can use the provided Android Tablet
  • 7.Subjects with a dedicated LAR or caretaker to address any study objectives in lieu of the subject.
  • 8.Subject/LAR who is willing to give informed consent for participation, able to comprehend and understand the responsibilities during treatment period and follow up period.

排除标准

  • 1.Subjects with mental illness and/or neuropsychiatric disorders.
  • 2.Subjects who are on anti-depressants, anti-psychotics and/or medication that may cause worsening in cognitive functions.
  • 3.Subjects with significant primary visual impairments.
  • 4.Any significant medical condition (e.g., significant psychiatric or neurological disorders, active alcohol/drug abuse, etc.), any medical condition that is unstable/poorly controlled or other factor (e.g., planned relocation) that the Investigator felt would interfere with study evaluations and study participation.
  • 5.Subjects who have participated in any clinical study within 3 months from the date of enrolment.
  • 6.Females who are pregnant or lactating or planning to become pregnant or unwilling to use double barrier method during the study period.
  • 7.Subjects who mentally unable to comprehend the responsibilities and adhere to the stipulations of the protocol.
  • 8.Subjects, who in the opinion of the Investigator/CRMC are not eligible for enrolment in the study.

研究者

发起方
Cerebrum Matter Limited

相似试验