Skip to main content
OpenTrials
Recruiting

NCT Number: NCT07413406

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

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.

Recruiting

Interested in participating?

Request Info

Key information

Age range

50 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

Caring for someone with dementia is often associated with high levels of stress, particularly when caregivers lack knowledge about how to manage behavioral and psychological symptoms of dementia (BPSD). Although educational resources for dementia caregivers are widely available, many are not designed using evidence-based learning principles that support long-term retention and application of information. Structured retrieval practice (SRP) is a learning strategy that enhances durable learning by requiring individuals to actively recall information over time while receiving corrective feedback.

This study is a longitudinal randomized controlled trial comparing an SRP-based educational intervention to a traditional reading-based education control condition. Informal caregivers of individuals living with dementia will be randomly assigned to one of two parallel arms. Both groups will receive educational content focused on managing dementia-related behavioral symptoms, coping strategies, and caregiver self-care; however, the format of instruction will differ by condition.

Outcomes will be assessed at baseline, and at 2-day, 2-week, and 2-month follow-up time points. Primary outcomes include caregiver knowledge retention, caregiving self-efficacy, perceived stress, and caregiver-reported severity of dementia-related behavioral symptoms. In addition, the study will evaluate intervention feasibility, acceptability, and adherence using self-report measures and backend program usage data.

Data will be collected either remotely or in person, depending on participant preference. The findings from this study will inform the development of evidence-based educational approaches that may be integrated into existing caregiver education programs and digital tools to better support families caring for individuals with dementia.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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

Exclusion criteria

  • 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

Treatment and study plan

Structured Retrieval Practice

Behavioral

The structured retrieval practice intervention is an educational learning approach designed to support durable knowledge retention through repeated active recall of information with corrective feedback. Caregivers will engage in retrieval-based learning activities focused on dementia symptom management, coping strategies, and self-care. Learning activities will be spaced over time, and participants will receive immediate feedback to support learning and retention.

Reading-Based Education

Behavioral

The reading-based education control condition consists of caregiver educational materials presented in a traditional reading format. Participants will review written information covering dementia-related behavioral symptoms, coping strategies, and caregiver self-care. Materials will be matched in content to the structured retrieval practice condition but will not include active retrieval or feedback components.

Primary outcomes

  1. Caregiver Knowledge Retention

    Time frame: Baseline; 2 days post-intervention; 2 weeks post-intervention; 2 months post-intervention

    Caregiver knowledge retention will be assessed using a researcher-developed multiple-choice assessment designed to measure factual and applied knowledge related to dementia symptom management and caregiver stress management. The assessment will consist of 64 items written at or below an 8th-grade reading level and tailored to each participant's selected learning content. Scores will reflect the total number of items answered correctly, with higher scores indicating greater knowledge retention.

  2. Caregiver Self-Efficacy

    Time frame: Baseline; 2 days post-intervention; 2 weeks post-intervention; 2 months post-intervention

    Caregiver self-efficacy will be measured using the Revised Scale for Caregiving Self-Efficacy (RSCSE). The RSCSE is a validated self-report instrument assessing caregivers' confidence in managing stress, responding to disruptive behaviors, and controlling upsetting thoughts. The measure includes three subscales, each consisting of five items rated on a 0% to 100% confidence scale. Subscale scores will be summed to create composite indices, with higher scores indicating greater caregiving self-efficacy.

  3. Caregiver Perceived Stress

    Time frame: Baseline; 2 days post-intervention; 2 weeks post-intervention; 2 months post-intervention

    Caregiver perceived stress will be assessed using the 10-item Perceived Stress Scale (PSS-10), a widely used self-report measure of perceived stress. Participants rate items on a 5-point Likert scale based on the frequency of stress-related experiences in the past month. Total scores range from 0 to 40, with higher scores indicating greater perceived stress.

Secondary outcomes

  1. Caregiver-Reported Dementia-Related Behavioral Symptoms

    Time frame: Baseline; 2 days post-intervention; 2 weeks post-intervention; 2 months post-intervention

    Caregiver perceptions of dementia-related behavioral and psychological symptoms will be assessed using the Neuropsychiatric Inventory Questionnaire (NPI-Q). Caregivers will indicate the presence and severity of symptoms across multiple behavioral domains. Composite scores will be calculated to reflect overall symptom presence and symptom severity, with higher scores indicating greater perceived symptom burden.

  2. Intervention Acceptability and Satisfaction

    Time frame: Immediately after completion of the intervention session.

    Participant satisfaction and acceptability will be assessed using the Client Satisfaction Questionnaire (CSQ-8), an 8-item self-report measure of satisfaction with health and educational interventions. Items are rated on a 4-point Likert scale, with higher scores indicating greater satisfaction and acceptability.

  3. Intervention Adherence

    Time frame: During intervention period

    Intervention adherence will be assessed using backend program usage data capturing participants' completion of intervention sessions and engagement with assigned learning activities. Adherence metrics will reflect the amount of intervention content completed and exposure to the intended learning schedule.

Study contacts

Contact information is provided by the study sponsor or research team.

Robert Ariel, PhD

CONTACT

[email protected]

757-455-3368

Uma Tauber, Ph.D

CONTACT

[email protected]

Sponsors and collaborators

Lead sponsor

Virginia Wesleyan University

Other

Collaborators

  • Texas Christian University

Registry information

Official study title

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

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Feb 17, 2026
Registry last updated
Feb 17, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.