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Engaging Caregivers in Dementia Care

Engaging Caregivers in the Care of Veterans With Dementia

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02552563
Enrollment
75
Registered
2015-09-17
Start date
2011-02-28
Completion date
2014-01-31
Last updated
2022-09-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dementia

Brief summary

This pilot study seeks to examine the extent to which, relative to usual care, a dementia care management program for veterans and their caregivers (CGs)improves patient (e.g., behavioral symptoms, delayed nursing home placement) and caregiver (e.g., CG mastery, burden, affect) outcomes.

Detailed description

Dementia care guidelines and pharmacological and non-pharmacological treatments have been shown to reduce symptom burden and rates of institutionalization for individuals with dementia. However, there remain a variety of factors that complicate dementia care management in primary care settings. Patient-centered, integrated care management programs that involve caregiver (CG) education and psychosocial support may help facilitate access to and use of services and improve outcomes. The aims of this pilot were to examine 1) whether, relative to usual care (UC), a dementia care management program is associated with improved CG (e.g., mastery, burden, affect) and patient (e.g., behavioral symptoms) outcomes, 2) if, relative to UC, participants enrolled in the program have greater perceived access to and use of medical, social, and community/VA services, and 3) whether the dementia care management program is feasible and acceptable to participants.

Interventions

The intervention involves two main components. The first component includes individualized dementia care management that involves regular and extended contact between the CG, care manager, and when appropriate, Veteran's primary care provider (PCP). The care manager monitors Veterans' symptoms via CG report, provides psychoeducation and support to CGs, influences adherence to guidelines by providing timely and tailored information to PCPs, and suggests appropriate care strategies and service referrals. The second major component is the Telehealth Education Program (TEP). For this pilot study, the program was modified for use with individual CGs and was formatted so that CGs could select from a menu of up to 7 modules covering various content areas evaluated during the course of the care management assessments (e.g., communication skills, behavioral management techniques, stress management and coping skills, long-term planning, etc.).

Sponsors

Corporal Michael J. Crescenz VA Medical Center
Lead SponsorFED

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Patient and caregiver 18 years of age or older * Patient is community dwelling * Patient has a confirmed dementia diagnosis and/or significant cognitive impairment (per provider or CG report) that is verified upon the RA's cognitive screening assessment (per veteran (BOMC, score of 16 or above) or informant (AD8, score of 2 or above) and/or chart review * CG lives with and/or provides care for the patient for an average of at least 4 hours per day. * Veteran provides assent to contact his/her representative to pursue study participation * Veteran representative as caregiver is willing and able to provide informed consent

Exclusion criteria

* Cognitive, hearing, visual, or other physical impairments leading to difficulty with assent/ informed consent process and/or assessment (veteran or caregiver)

Design outcomes

Primary

MeasureTime frameDescription
Revised Memory and Behavior Problems Checklist (RMBPC)Change in frequency and distress from baseline to 3 and 6 month follow-upFrequency of care recipient dementia-related behaviors and associated caregiver distress
Neuropsychiatric Inventory Questionnaire (NPI-Q)Change in frequency and distress from baseline to 3 and 6 month follow-upFrequency of care recipient neuropsychiatric symptoms and associated caregiver distress
Zarit Burden InterviewChange in burden from baseline to 3 and 6 month follow-upPerceived caregiver burden

Secondary

MeasureTime frameDescription
Pearlin Stress and Coping ScaleChange in coping skills from baseline to 3 and 6 month follow-upCaregiver coping strategies
Lawton Caregiving and Stress Process ScalesChange in caregiver mastery from baseine to 3 and 6 month follow-upCaregiver mastery

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026