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临床试验/NCT03622840
NCT03622840终止不适用

Impact of Individual Cognitive Remediation for Parkinson's Disease

New York Institute of Technology2 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2018年7月12日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
入组人数
12
试验地点
2
主要终点
Change of Test of Memory and Learning (TOMAL) score

研究概览

简要总结

This is an interventional clinical trial that will be conducted as a pilot project. Investigators hope to conduct the study to obtain at least 10 study completers.

The plan is to screen 20 Parkinson's Disease (PD) patients attending the Academic Health Care Center (AHCC) at NYIT College of Osteopathic Medicine clinic and enroll the eligible candidates based on the inclusion and exclusion criteria. Subjects will have 11 study visits over the 11-week period. Subjects cognition will be assessed using a paper-based Test of Memory and Learning (TOMAL) tool. The same tool will be used to asses and compare the cognition at baseline, and end study visits. The weekly 30-mins of cognitive remediation exercises will be done using the Brain. HQ cognitive remediation software.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
40 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Subjects must be between 40 and 75 years old (including both ages) at the time of study screening.
  • Subjects must have a diagnosis of Parkinson's Disease by a physician.
  • Subjects must demonstrate adequate decisional capacity, in the judgment of the consenting study staff member, to make a choice about participating in this research study.
  • Subjects must have been clinically stable (non-acute) for 2 weeks prior to consent; in the judgment of the Investigator.
  • Subjects with a cognition level between Impaired and Average (scaled score between 4-12 or Index Score between 70-110) based on TOMAL Cognitive assessment at Visit 1
  • Subjects must have the visual, auditory, and motor capacity to use the intervention in the judgment of the Principal Investigator.

排除标准

  • Subjects who are participating in a concurrent research study or another interventional clinical trial 30 days prior to consenting.
  • Subjects having a history of mental retardation or pervasive developmental disorder; or other co-morbid neurological disorder (e.g., epilepsy.)
  • Subjects who appear to be intoxicated or under the influence of a controlled substance on any day of assessment must be rescheduled and may be discontinued based upon the discretion of the investigator
  • Subjects on medications that affect the cognition in the last 12 hours prior to the study visits that assess the cognitive functions

研究组 & 干预措施

Parkinson's disease patients with cognitive impairment

Other

Online cognitive remediation program.

干预措施: Cognitive Remediation (Behavioral)

结局指标

主要结局

Change of Test of Memory and Learning (TOMAL) score

时间窗: Baseline and 11 weeks

Paper based memory and attention test administered at the beginning and end of the study

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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