跳至主要内容
临床试验/NCT04915040
NCT04915040已完成不适用

Management of Depression and Social Isolation in Older Adults With Dementia With Home-based Telehealth Delivered Behavioral Activation + Caregiver Facilitation.

The University of Texas Health Science Center, Houston2 个研究点 分布在 1 个国家目标入组 7 人开始时间: 2021年7月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
7
试验地点
2
主要终点
Feasibility of data collection as assessed by percent of missing data

研究概览

简要总结

The purpose of this study is to evaluate the feasibility of using behavioral activation therapy with caregiver support delivered via telemedicine to older adults with depression and probable mild dementia.

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
65 Years 至 —(Older Adult)
性别
All
接受健康志愿者

入选标准

  • Participant Eligibility Criteria:
  • able to speak and understand English;
  • a diagnosis of mild dementia, as determined by a Clinical Dementia Rating interview Sum of Boxes (CDR-SB) score in the mild range as defined by a score of 4.5 - 9.0;
  • and able to provide informed consent.
  • Caregiver Eligibility Criteria.
  • Beck Depression Inventory (BDI) score below clinical cutoff for depression and able to provide informed consent.

排除标准

  • Participant exclusion criteria:
  • presence of suicidal ideation with clear intent,
  • concurrent enrollment in another clinical trial for depression,
  • substance use disorder.
  • Caregiver exclusion criteria:
  • Active psychosis or significant dementia at screening;
  • presence of suicidal ideation with clear intent.

结局指标

主要结局

Feasibility of data collection as assessed by percent of missing data

时间窗: Week 8

Change in Depression as measured by the Geriatric Depression Scale

时间窗: Week 0, Week 4, Week 8

15-item self-report for each construct (yes/no) . Score goes from 1 to 15, a higher number indicates presence of depression.

Feasibility of recruitment as assessed by number of participants enrolled in the study

时间窗: Week 0

Feasibility of retention as assessed by number of participants who complete at least 6 sessions

时间窗: Week 8

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

Michael Bradley Cannell

Associate Professor

The University of Texas Health Science Center, Houston

研究点 (2)

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