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临床试验/NCT02945085
NCT02945085已完成不适用

3D Team Care for Cognitively Vulnerable Older Adults

UConn Health1 个研究点 分布在 1 个国家目标入组 506 人开始时间: 2017年3月6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
发起方
入组人数
506
试验地点
1
主要终点
Proportion hospitalized or used emergency department without hospitalization

研究概览

简要总结

This study addresses how to achieve better outcomes for cognitively vulnerable community-dwelling older adults and their families. Cognitive vulnerability means living with dementia, depression, and/or a recent episode of delirium (the 3Ds). The investigators will test the effectiveness of a team care model focused on the 3Ds (Home Based Care Team) guided by nurse practitioners with expertise in geriatrics and geriatric psychiatry. Specific aims are to determine Home Based Care Team effects on hospitalization or emergency department use, and other outcomes including depression, disability, and quality of life.

详细描述

This study addresses how to achieve better outcomes for cognitively vulnerable community-dwelling older adults and their families. Cognitive vulnerability means living with dementia, depression, and/or a recent episode of delirium (the 3Ds). Cognitive vulnerability in older adults is often overlooked by primary care and hospital-based providers, and represents a marker for overall vulnerability or frailty often missed when disease-specific approaches are emphasized in the care for older adults. Such patients often cannot adequately self-manage their comorbidities. Many studies of older adults and their families have demonstrated the great burden of living with cognitive vulnerability. The investigators will test the effectiveness of a team care model focused on the 3Ds (Home Based Care Team) guided by nurse practitioners with geriatrics expertise. Other team member disciplines will include pharmacy, social work, occupational and physical therapy, nutrition, and community health worker. Long-term objectives are to determine whether this care model can become a widely available approach for improving healthcare systems for older adults with cognitive vulnerability and their families, while improving outcomes of importance to these patients and families. A project Steering Committee, including cognitively vulnerable patients and family caregivers, will provide extensive input into many aspects of the research process.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

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

入选标准

  • •Evidence of dementia, depression, and/or delirium, based on diagnostic codes found in medical claims data and based on screening at time of study screening.
  • •Living in the community, including assisted living facility, at time of randomization
  • •Plan to live in geographic area for 12 months
  • •Speak or understand English
  • •Willing to be randomly assigned to intervention or active comparator group

排除标准

  • •Diagnosed schizophrenia or bipolar disorder
  • •Bedbound and non-communicative
  • •Life expectancy <12 months
  • •Already enrolled in active comparator program
  • •For individuals with dementia, family caregiver is unavailable or unwilling to enroll in study

研究组 & 干预措施

Home Based Care Team

Experimental

Primarily in-home treatment provided by team led by nurse practitioner with geriatrics and geriatric psychiatry expertise.

干预措施: Home Based Care Team (Other)

Telephone Based Care Team

Active Comparator

Primarily telephone-based treatment provided by existing care management program offered by collaborating Medicare Advantage insurer.

干预措施: Telephone Based Care Team (Other)

结局指标

主要结局

Proportion hospitalized or used emergency department without hospitalization

时间窗: 12 months

Evidence of hospitalization or visit to emergency department without hospital admission will be based on data from the Medicare Advantage insurer's medical claims data warehouse.

次要结局

  • Patient Health Questionnaire (PHQ9)(12 months)
  • Caregiver Assessment of Function and Upset (CAFU)(12 months)
  • Family caregiver perceived well-being(12 months)

研究者

发起方
UConn Health
申办方类型
Other
责任方
Principal Investigator
主要研究者

Fortinsky, Richard

Professor

UConn Health

研究点 (1)

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