Dementia Caregivers' Link to Assistance and Resources

Phase

N/A

Condition

Dementia

Treatment

Dementia Caregivers' Link to Assistance and Resources (DECLARE)

Clinical Study ID

NCT06860035

2298464

K01AG081502

All Genders
Accepts Healthy Volunteers

Study Summary

The goal of this clinical trial is to learn if the Dementia Caregivers' Link to Assistance and Resources (DECLARE) program can improve support of, and engagement with, caregivers of home health patients with dementia. DECLARE includes a caregiver self-assessment that is reported in the home health patient record, and increased access to social work for cases including dementia caregivers. The main questions we aim to answer are:

Will most caregivers who are offered the chance to complete an assessment choose to do so?
Will clinicians report that the assessment information was useful?
Will the rate of social work access increase for cases with patients with dementia who have involved family caregivers?

Researchers will compare DECLARE to usual care to see if taking part in the program increases caregiver self-efficacy and access to social work.

Participants will:

Answer a short series of assessment questions and questions about their caregiving experiences at the beginning of the home health episode.
Receive a social work visit from a Licensed Social Worker trained in dementia care.
Answer a series of follow-up questions about their caregiving experiences at the end of the home health episode.

Eligibility Criteria

Inclusion

Inclusion Criteria:

Individual must be listed as the caregiver of record for a patient receiving homehealth care from the partner home health agency and have a phone number on file; thepatient must meet the inclusion criteria listed below.
Home health patient (care recipient) must have a documented dementia diagnosis onthe home health assessment, be 65 years or older, and have Traditional Medicare orMedicare Advantage as their primary payer for the home health episode.

Exclusion

Exclusion Criteria:

Caregivers are excluded if they are unable to communicate in English.

Study Design

Dementia Caregivers' Link to Assistance and Resources (DECLARE)

May 05, 2025

June 30, 2026

Study Description

The goal of the present study is to pilot test a novel ADRD caregiver assessment instrument, designed specifically for the HH setting, with the ultimate aims of improving caregiver self-efficacy and increasing access to social work during HH for cases involving caregivers who are experiencing high strain and/or low preparedness for caregiving. This is the Dementia Caregivers' Link to Assistance and Resources (DECLARE) program. Specific Aims include: (1) Contacting eligible caregivers to field a caregiver self-assessment and sharing caregiver responses with frontline staff in the patient record, (2) Identifying cases for social work access, and (3) Assessing the feasibility, acceptability, and impact on caregiver outcomes of the activities described in Aims 1 and 2.

This is an embedded Pragmatic Clinical Trial (ePCT) within the VNS Health home health agency. We will implement the intervention in 4 "treatment" branches (includes 8 clinical teams) and will compare to 6 "control" branches (includes 12 clinical teams). Treatment branches will receive the DECLARE intervention described in the following section and control branches will not have any intervention. In both arms, we will conduct baseline and follow-up telephone surveys with caregivers of eligible cases to gather outcomes data. We anticipate a 12-month trial, with regular analytic checkpoints to assess for potential issues and make revisions as needed.

We will identify eligible cases based on the start of care OASIS (home health patients 65 and older with diagnosed ADRD, a caregiver on record with a phone number, and payment through Traditional Medicare or a Medicare Advantage plan managed by VNS Health. Research staff will contact the caregiver of record via telephone to field the self-assessment survey. In treatment branches, caregiver responses will be entered into a secure survey platform (RedCAP) and uploaded to the patient electronic health record (HomeCare HomeBase) as a care coordination note. For cases without a social work order, the research team will either (a) contact the Clinical Field Manager to request a social work order, if none exists or (b) contact the appropriate social worker if a social work order is already in place. We anticipate 150 participants (60 from treatment branches and 90 from control branches).

Connect with a study center

VNS Health Home Care
New York, New York 10017
United States
Active - Recruiting

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.