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Development of Measures to Screen for Financial Hardship in Alzheimer's Disease and Dementia
NCT06922188 · Fred Hutchinson Cancer Center
In plain English
Click the button to translate this study into plain language — what it is, who qualifies, and what participation looks like.
About this study
This study investigates the financial hardship experienced by individuals with Alzheimer's Disease and Alzheimer's Disease-Related Dementias (AD/ADRD) and their caregivers. The research comprises qualitative interviews, content validation surveys, and quantitative data collection to assess financial stressors, caregiving costs, and coping mechanisms.
The first phase involves conducting semi-structured interviews with individuals diagnosed with AD/ADRD and their caregivers. These interviews will be conducted virtually, by phone, or in person, with most expected to take place remotely. Informed consent will be obtained either verbally or through signed documentation, as appropriate. Participants will be interviewed separately to ensure privacy, particularly in cases where both the patient and their caregiver are involved. The interview guide will explore changes in financial circumstances before and after diagnosis, general and specific aspects of financial hardship-including financial stress, financial strain, and asset depletion-contributing factors to financial hardship, strategies used to mitigate financial burdens, and the impact of financial hardship on well-being, decision-making, and care options. Additionally, the study will examine financial management practices, including the transition of financial responsibility from the patient to caregivers, as well as the role of caregivers and social networks in financial management and hardship buffering. Interviews will be recorded and transcribed, with Spanish transcripts translated into English. Participants will receive a small incentive for participation. If a caregiver or patient expresses interest in the other member of the dyad participating, they will be contacted via email or phone for potential enrollment.
Following the qualitative phase, a structured survey will be distributed to validate the relevance and applicability of financial hardship indicators identified during the interviews. Participants will receive an email with a study invitation and a survey link, where they will review definitions of financial hardship domains, assess the relevance of each survey item based on the perspective of the caregiver and patient, and provide demographic and job-related information. To optimize participant burden, randomized subsets of the survey will be assigned if the item bank is extensive. Participants will receive a small incentive for survey completion.
After eligibility screening, participants will complete a financial hardship survey either online or via mail. Online participants will review an electronic consent statement before proceeding, while mail-in participants will sign and return a consent form along with their completed survey using a prepaid return envelope. The survey will collect data on financial stressors, caregiving costs, and coping mechanisms. Participants will receive informational handouts on financial support resources and mental health care services. The study will examine financial caregiving networks and social support structures, as well as how financial hardship influences long-term care decisions and overall well-being. Participants will be compensated for their time and contribution to the study.
Quality control and data management processes will ensure the integrity and accuracy of study data. Surveys and interview transcripts will undergo validation checks to ensure data consistency. Data will be categorized using structured coding frameworks. A mixed-methods approach will be employed for analysis, using qualitative thematic analysis for interview data and statistical modeling for survey responses.
This study aims to improve the understanding of financial hardship among individuals with AD/ADRD and their caregivers, providing critical insights to inform policy interventions and support strategies for affected individuals and their families.
Eligibility criteria
Inclusion Criteria:
* Adults aged 18 years or older
* One of the following:
* Clinical diagnosis of Alzheimer's disease or related dementia
* Being a caregiver to individuals with clinical diagnosis of Alzheimer's disease or related dementia
* Able to read and speak English or Spanish
* Able to provide informed consent
* Residing in the United States
Exclusion Criteria:
• Cognitive impairment precluding informed consent
Study design
Enrollment target: 2460 participants
Age groups: adult, older_adult
Timeline
Starts: 2025-03-31
Estimated completion: 2029-12-18
Last updated: 2026-02-19
Primary outcomes
- • Thematic Analysis of Qualitative Interviews to Inform Measure Development (Month 6 to Month 18 of the study)
- • Internal Consistency of Financial Hardship Item Banks (At initial survey administration (approximately Month 19 to month 42 of the study))
- • Construct Validity of Financial Hardship Item Banks (At initial survey administration (approximately Month 19 to month 42 of the study))
Sponsor
Fred Hutchinson Cancer Center · other
With: National Institute on Aging (NIA), Johns Hopkins University, University of North Carolina, Chapel Hill
Contacts & investigators
ContactDiana K Lowry, MPH · contact · dlowry@fredhutch.org · 206-667-7372
ContactSalene Jones, PhD, MA · contact · smjones3@fredhutch.org · 206-667-6976
InvestigatorSalene MW Jones, PhD, MA · principal_investigator, Fred Hutchinson Cancer Center
All locations (1)
Fred Hutchinson Cancer CenterRecruiting
Seattle, Washington, United States