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
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