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NCT07413406Recruiting

Comparing Structured Retrieval Practice and Reading-Based Education for Dementia Caregivers

A Randomized Controlled Trial of a Care Partner-Centered Structured Retrieval Practice Intervention for Dementia Caregiver Education and Well-Being

Source: ClinicalTrials.gov · Last updated 17 Feb 2026

Brief summary (registry, in English)

Caring for a person living with dementia can be stressful, and many family caregivers report limited access to effective educational resources for managing dementia-related behaviors and caregiver stress. This study will evaluate a learning-based educational intervention called structured retrieval practice (SRP), which is designed to improve long-term learning by encouraging repeated recall of information with feedback. Informal dementia caregivers will be randomly assigned to learn caregiving and self-care strategies using either SRP or a traditional reading-based educational approach. Participants will be assessed on their knowledge, confidence in caregiving skills, stress levels, and perceptions of dementia-related behavioral symptoms over multiple follow-up periods. The study will also examine whether the SRP intervention is feasible and acceptable for caregivers in real-world settings.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
65 (estimated)
First submitted
4 Feb 2026
Start date
3 Oct 2025
Primary completion date
30 Jun 2026
Lead sponsor
Virginia Wesleyan University
NCT number
NCT07413406

What you commit to

  • Study type: Interventional
  • Planned participants: 65
  • From 3 Oct 2025 to the primary completion date, 30 Jun 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Caregivers providing assistance to an individual without evidence of cognitive - impairment, as determined by a dementia screening interview (AD8 score \< 2)
  • Failure to meet study screening requirements or provide informed consent

Age

  • Caregivers younger than 50 years of age

Other

  • Paid or professional caregivers (e.g., home health aides)
  • Caregivers reporting low perceived stress (PSS-10 score below 14)
  • Inability to complete study procedures due to cognitive, sensory, or technological limitations

Who the study is looking for

  • 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

Age in the registry: 50 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Virginia Wesleyan University
Coordinator of this site? Confirm its status
Virginia BeachUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.