NCT05478681已完成不适用
Home-based tDCS for Behavioral Symptoms in Alzheimer's Disease and Related Dementias (ADRD)
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 3
- 试验地点
- 4
- 主要终点
- Acceptability of the tDCS Treatment as Assessed by the tDCS Acceptability Questionnaire
研究概览
简要总结
The purpose of this study is to assess acceptability, and safety of providing tDCS to ADRD patients with behavioral symptoms and to assess the efficacy of tDCS for ADRD-related symptoms, mainly behavioral symptoms.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 60 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •have ADRD and clinically-meaningful behavioral symptoms
- •have a caregiver willing to participate in the study
- •can speak and read English
- •have stable doses of medications for at least one month
排除标准
- •any unstable concurrent medical conditions
- •history of brain surgery
- •intracranial metal implantation
- •current alcohol/substance use disorder
结局指标
主要结局
Acceptability of the tDCS Treatment as Assessed by the tDCS Acceptability Questionnaire
时间窗: week 12
The tDCS acceptability questionnaire has a total score from 0 to 100, a higher score indicates higher acceptance of the tDCS treatment.
Safety as Assessed by the Side Effects Questionnaire
时间窗: week 6
side effects include itching, burning, headache, fatigue, and dizziness.
次要结局
- Apathy as Assessed by the Brief Dimensional Apathy Scale (b-DAS)(Baseline, Week 6 and Week 12.)
- Dementia-related Behavioral Symptoms as Assessed by the Neuropsychiatric Inventory (NPI-Q) Scale(Baseline, week 2, week 4, week 6, week 12)
- Depressive Symptoms as Assessed by the Cornell Scale for Depression in Dementia (CSDD)(Baseline, Week 6 and Week 12.)
- Cognition as Evaluated by the Mini-Mental State Examination (MMSE)(Baseline, Week 6 and Week 12.)
研究者
Kendra Anderson
Assistant Professor
The University of Texas Health Science Center, Houston
研究点 (4)
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