3D Team Care for Cognitively Vulnerable Older Adults

Depression Clinical Trial

Official title:

3D Team Care for Cognitively Vulnerable Older Adults

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02945085
• Other study ID #: 17-021-1
• Status: Recruiting
• Phase: N/A
• Start date: March 6, 2017
• Est. completion date: July 31, 2024

Study information

• Verified date: June 2023
• Source: UConn Health
• Contact: Richard H Fortinsky, PhD
• Phone: 860-679-8069
• Email: fortinsky[@]uchc.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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.

Description:

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.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 576
• Est. completion date: July 31, 2024
• Est. primary completion date: July 31, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 65 Years and older

Eligibility

Inclusion Criteria:

• 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

Exclusion Criteria:

• 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

Related Conditions & MeSH terms

• Delirium
• Dementia
• Depression

Intervention

Other:
• Home Based Care Team
Clinical team will conduct comprehensive clinical assessments focused on cognitive impairment and depression, conduct comprehensive medication review and reconciliation, offer Problem Solving Therapy, and offer brief occupational therapy, physical therapy, nutrition, and social support services.
• Telephone Based Care Team
Telephone contact will be made by nurses. Depending on level of need, follow up telephone and, in some cases, in home visits will be made by nurse or social worker from care management program.

Locations

Country	Name	City	State
United States	UConn Center on Aging	Farmington	Connecticut

Sponsors (3)

Lead Sponsor	Collaborator
UConn Health	Patient-Centered Outcomes Research Institute, University of Connecticut

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	World Health Organization (WHO) Disability Assessment Schedule, 12 item short form.	This measure yields a score for each individual reflecting self-reported degree of difficulty performing physical activities in the home and community. Individual scores will be aggregated into group mean scores to compare intervention and active comparator groups on this outcome.	12 months
Other	Quality of Life-Alzheimer's Disease Scale (QOL-AD)	This measure, used with individuals with dementia, yields a score for each individual reflecting self-ratings of poor, fair, good, or excellent on 13 items. Individual scores will be aggregated into group mean scores to compare intervention and active comparator groups on this outcome.	12 months
Other	Neuropsychiatric Inventory (NPI-C)	This measure yields a single score that accounts for both frequency and severity of 14 neuropsychiatric symptoms. Family caregivers provide this information in a structured interview format. Individual scores will be aggregated into group mean scores to compare intervention and active comparator groups on this outcome.	12 months
Other	Center for Epidemiologic Studies-Depression Scale (CES-D)	This measure will be used to determine severity of depression among family caregivers enrolled in the study.This measure yields a score for each individual reflecting frequency of 20 depression-related symptoms within the previous two weeks. Individual scores will be aggregated into group mean scores to compare intervention and active comparator groups on this outcome.	12 months
Other	Zarit Burden Scale, 12-item short form	This measure will be used to determine severity of caregiving-related burden among family caregivers who enroll in the study.This measure yields a score for each individual based on self-reports by family caregivers on the degree of caregiving impact on emotional, physical, social, and financial aspects of life. Individual scores will be aggregated into group mean scores to compare intervention and active comparator groups on this outcome.	12 months
Primary	Proportion hospitalized or used emergency department without hospitalization	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.	12 months
Secondary	GRID Hamilton Rating Scale for Depression (GRID-HAMD), 17-item version.	This measure yields a score for each individual reflecting both frequency and intensity of all depression-related symptoms included in the structured interview. This outcome will be used for study participants with depression but not dementia or recent episode of delirium at baseline. Individual scores will be aggregated into group mean scores to compare intervention and active comparator groups on this outcome.	12 months
Secondary	Caregiver Assessment of Function and Upset (CAFU)	This measure yields a score for each individual reflecting level of assistance required to conduct 7 self-care activities of daily living (ADLs) and 8 instrumental ADLs. In a structured interview format, family members report these items for their relatives with dementia and/or a recent history of delirium. Individual scores will be aggregated into group mean scores to compare intervention and active comparator groups on this outcome.	12 months
Secondary	Family caregiver perceived well-being	Self-reported well-being among family caregivers who enroll in the study	12 months