Actively Recruiting
A Randomized Controlled Trial of a Care Partner-Centered Structured Retrieval Practice Intervention for Dementia Caregiver Education and Well-Being
Led by Virginia Wesleyan University · Updated on 2026-02-17
65
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
V
Virginia Wesleyan University
Lead Sponsor
T
Texas Christian University
Collaborating Sponsor
AI-Summary
What this Trial Is About
This research aims to support informal caregivers of people living with dementia by comparing two educational approaches designed to improve caregiving knowledge, skills, and stress management. The study focuses on caregivers aged 50 and older who report moderate to high stress. Researchers will evaluate a learning-based method called structured retrieval practice (SRP) that encourages repeated recall of information with feedback, compared to traditional reading-based education. The goal is to see which approach better supports caregivers in managing dementia-related behaviors and their own well-being. Participants will be randomly assigned to one of two groups. One group will receive education using SRP, which involves active recall exercises spaced over time with immediate feedback on managing dementia symptoms, coping, and self-care. The other group will receive the same educational content in a traditional reading format without active recall or feedback. Both interventions focus on caregiver strategies and dementia-related behavioral symptoms. Caregivers will be assessed at the start and then at 2 days, 2 weeks, and 2 months after the intervention. Measurements include knowledge retention, confidence in caregiving skills, perceived stress, and reports of dementia-related behavioral symptoms. The study will also gather feedback on how acceptable and feasible the SRP intervention is, tracking participation and adherence. Data collection can be done remotely or in person, based on participant preference, and the study runs until June 2026.
CONDITIONS
Brief Title
Comparing Structured Retrieval Practice and Reading-Based Education for Dementia Caregivers
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 50 years or older
- Informal (unpaid) caregiver for a family member or friend living with dementia
- Providing ongoing assistance or support to the individual with dementia
- Reports moderate to high perceived stress, defined as a score of 14 or higher on the Perceived Stress Scale (PSS-10)
- Able to speak and read English
- Able to complete study procedures either in person or remotely
- Has access to a computer, tablet, or smartphone with internet access
- Willing and able to provide informed consent
You will not qualify if you...
- Paid or professional caregivers (e.g., home health aides)
- Caregivers younger than 50 years of age
- Caregivers reporting low perceived stress (PSS-10 score below 14)
- Caregivers providing assistance to an individual without evidence of cognitive impairment, as determined by a dementia screening interview (AD8 score < 2)
- Inability to complete study procedures due to cognitive, sensory, or technological limitations
- Failure to meet study screening requirements or provide informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person or remote)
Duration - Single session with follow-up assessments over 2 months
Participants receive caregiver education through either structured retrieval practice or traditional reading-based materials focused on managing dementia-related behavioral symptoms, coping strategies, and caregiver self-care.
1 baseline session (in-person or remote) plus follow-up assessments at 2 days, 2 weeks, and 2 months
Duration - 2 months post-intervention
Participants complete follow-up assessments to evaluate caregiver knowledge retention, self-efficacy, perceived stress, and caregiver-reported dementia-related behavioral symptoms after the educational intervention.
3 follow-up assessments at 2 days, 2 weeks, and 2 months post-intervention
Trial Site Locations
Total: 1 location
1
Virginia Wesleyan University
Virginia Beach, Virginia, United States, 23455
Actively Recruiting
Research Team
R
Robert Ariel, PhD
U
Uma Tauber, Ph.D
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
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