CompletedNot Applicable

WECARE: A Behavioral Intervention for Dementia Caregivers

United States48 participantsStarted 2023-09-01

Plain-language summary

This study aims to pilot test a culturally tailored behavioral intervention called "WECARE" to enhance caregiving mastery and improve psychosocial wellbeing of Chinese American family caregivers of persons with Alzheimer's Disease and related dementia.

Who can participate

Age range

21 Years – 90 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

. 21 years or older,
. self-identified as Chinese or Chinese American,
. speak and read Chinese (Mandarin or Cantonese),
. own a smartphone and use WeChat,
. living in Washington DC metropolitan, and
. currently care for a family member with ADRD and provide care for at least 10 hours a week.

Exclusion criteria

. do not read or speak Chinese,
. care-recipient is in hospice care or have a life expectancy less than 6 months,
. signs of severe intellectual deficits or psychotic disorders, or
. unable to provide informed consent.

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Efficacy of Behavioral Intervention in Change From Baseline in Depressive Symptoms

Timeframe: Baseline, and Follow-Up at Weeks 11-12 (4 to 5 weeks after completion of the intervention)

Trial details

NCT IDNCT05992467

SponsorGeorge Mason University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-08-31

Results submitted2025-08-21

View on ClinicalTrials.gov More Caregiver Burden trials