Caring for Dementia Caregivers in Ethnic Immigrant Communities
1 other identifier
interventional
120
1 country
1
Brief Summary
Many caregivers of people with Alzheimer's disease or other dementias-especially those in immigrant communities who don't speak English well-don't get access to helpful, proven support programs. This is especially true for Korean American caregivers. To address this, the investigative team adapted an existing caregiver support program (called the Savvy Caregiver Program) to better fit Korean culture and language. This new version, called K-Savvy, is a 6-week online program taught in Korean. In an earlier small study, K-Savvy worked well: caregivers found it helpful, were willing to use it, and showed fewer symptoms of depression. Now, the investigative team wants to study it more carefully to see how well it really works and why. The study has two main goals: Goal 1: The investigative team will measure whether K-Savvy improves caregivers' well-being-specifically whether it reduces stress and depression and helps them feel more positive about caregiving. The investigative team will also look at why it works, focusing on whether it changes how caregivers think about their situation (for example, feeling less overwhelmed and more confident). Goal 2: The investigative team will talk directly with caregivers and program instructors to understand their experiences with K-Savvy. This will help the investigative team learn what worked well, what didn't, and why.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started May 2026
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 17, 2026
CompletedFirst Posted
Study publicly available on registry
April 24, 2026
CompletedStudy Start
First participant enrolled
May 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 30, 2030
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 30, 2030
April 30, 2026
April 1, 2026
4.7 years
April 17, 2026
April 28, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
depressive symptoms
symptoms of depression assessed with Patient Health Questionnaire-9, range from 0 to 27 (higher scores indicating greater depressive symptoms)
from enrollment to 6-month follow-up
Secondary Outcomes (1)
caregiver burden
from enrollment to 6-month follow-up
Study Arms (3)
K-Savvy
EXPERIMENTALimmediate enrollment in K-Savvy, 6-week online psychoeducation program
Healthy Living
ACTIVE COMPARATORenrollment in a 6-week online health education program and subsequent enrollment in K-Savvy
waitlist control
OTHERK-Savvy enrollment after a waiting period
Interventions
Funded by the NIA (R21AG071790, PI: Jang), our team successfully completed linguistic and cultural adaptations of the Savvy Caregiver Program (SCP) for Korean American dementia caregivers with limited English Proficiency. The Korean version of the SCP (K-Savvy) has shown high feasibility, acceptability, and initial efficacy.
6-week online health education for Korean Americans with limited English proficiency
Eligibility Criteria
You may qualify if:
- Self-identified Korean American adults aged 18 or older Provide care for a family member with dementia as a primary caregiver Primary caregiver defined as providing a minimum of 10 hours per week of in-home caregiving to a family member Speak English less than "very well" Able to attend virtual classes using an electronic device with Internet access
You may not qualify if:
- Individuals with severe depression (Patient Health Questionnaire \[PHQ-9\] score ≥ 20), as K-Savvy is not a mental health treatment program
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Southern California
Los Angeles, California, 90089, United States
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- SEQUENTIAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
April 17, 2026
First Posted
April 24, 2026
Study Start
May 1, 2026
Primary Completion (Estimated)
December 30, 2030
Study Completion (Estimated)
December 30, 2030
Last Updated
April 30, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL
Study results will be disseminated to the scientific community. De-identified individual participant data (IPD) collected in this study will be made available to qualified researchers upon reasonable request. The shared dataset will include variables necessary to replicate study findings, along with relevant documentation (e.g., data dictionaries and study protocols). Data sharing will be conducted in compliance with human subjects protection regulations and the University of Southern California Institutional Review Board, and in accordance with National Institutes of Health data sharing policies. Access may require a data use agreement to ensure appropriate use and protection of participant confidentiality.