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临床试验/NCT07541144
NCT07541144已完成不适用

Group Digital Gaming: Experiences of Older Adults Living With Dementia in an Activity for Cognitive Impairment

George Mason University1 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2023年8月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
24
试验地点
1
主要终点
Montreal Cognitive Assessment (MoCA):

研究概览

简要总结

The study examines the effects of a group digital gaming intervention on cognitive function, mood, and behaviors in people with early to moderate levels of dementia, using Obie Technology by employing a pretest and posttest design with a mixed methods approach.

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

性别
All
接受健康志愿者

入选标准

  • individuals with early-stage dementia (MoCA scores ≥ 20) or moderate-stage dementia (MoCA scores 10-19) who were able to participate in the intervention activity twice weekly for 20 weeks.

排除标准

  • 未提供

研究组 & 干预措施

Group-Based Digital Gaming

Experimental

干预措施: Group-Based Digital Gaming (Behavioral)

结局指标

主要结局

Montreal Cognitive Assessment (MoCA):

时间窗: Before the intervention (baseline), at the end of week 10, and at the end of the intervention (after 20 weeks of the study).

Montreal Cognitive Assessment contains 30 items and takes approximately 10 minutes to administer assessing multiple cognitive domains such as short-term memory, visuospatial abilities, and abstraction. The minimum total score is 0 and the maximum tota score is 30. The higher scores are associated with better cognitive function, and a score of 26 and higher is considered normal.

Neuropsychiatric Inventory Questionnaire (NPI-Q)

时间窗: Before the intervention (baseline), at the end of week 10, and at the end of the intervention (after 20 weeks of the study).

Neuropsychiatric Inventory Questionnaire is an informant-based instrument that assesses the possible presence of 12 neuropsychiatric symptoms in dementia, including delusions, hallucinations, agitation/aggression, dysphoria/depression, anxiety, euphoria/elation, apathy/indifference, disinhibition, irritability/lability, aberrant motor behaviors, night-time behavioral disturbances and appetite/eating disturbances. It asks the presence each symptom and its severity with a 3-point scale. The minimum total score is 0, and the maximum total score is 36. Higher scores indicate more severe neuropsychiatric symptoms and/or greater caregiver distress. It is shown to be a reliable and valid instrument. Most informants will be able to complete this instrument in less than five minutes.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Megumi Inoue

Professor

George Mason University

研究点 (1)

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