Clinical trial Recruiting at 1 site Phase 1 Interventional Ages 18 and up

Online education to help dementia caregivers apply and teach ways to manage behavioral symptoms

Official title: Exploration of Structure Retrieval Practice to Support Caregivers' Knowledge Transfer

Run by Texas Christian University · NCT07377331 · Data updated 2026-11-12

This project will test whether a short online training called Structured Retrieval Practice helps adult informal caregivers of people with dementia better apply and explain strategies for managing behavioral and psychological symptoms.

More Dementia trials

Quick facts

PhasePhase 1
Study typeInterventional
Ages18 Years and up
SexAll
Enrollment60 (estimated)
SponsorTexas Christian University
Academic / other
Locations2 sites (Fort Worth, Texas and 1 other locations)
StatusRecruiting
StartedNovember 1, 2025
Main results expectedAugust 15, 2026
Study endsAugust 15, 2026
Registry record updatedJanuary 29, 2026
Trial IDNCT07377331 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal participants are adult (18+) informal caregivers currently helping someone with dementia who read and speak English, have no cognitive impairment that prevents consent, and (if remote) have access to a tablet, laptop, or desktop computer.

Probably not a fit

Professional caregivers, former caregivers who are not currently providing care, caregivers for people with normal cognition, or individuals with cognitive impairments that prevent consent are not eligible and likely would not benefit from this intervention.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This Phase 1 interventional pilot delivers a brief online educational intervention (Structured Retrieval Practice) to informal caregivers of people with dementia to extend prior work on caregiver training. Participants complete remote or site-based activities designed to strengthen memory for management strategies and to practice applying those strategies to real-world examples of behavioral and psychological symptoms of dementia (BPSD). The study enrolls adult, English-speaking informal caregivers without cognitive impairment who are currently providing care, and excludes professional or former caregivers not actively caregiving. Activities are conducted through Texas Christian University and Virginia Wesleyan University with remote participation allowed for those with a tablet, laptop, or desktop.

Why it matters

Potential benefit: If successful, caregivers may be better able to use and teach practical strategies for managing BPSD, which could reduce troublesome behaviors and caregiver stress.

How similar studies have gone: Caregiver education programs and retrieval-practice learning methods have shown benefits for knowledge retention and coping in prior research, but applying structured retrieval practice specifically to real-world caregiver behavior transfer is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* informal caregivers
* 18+ years old
* Read and speak English
* free of cognitive impairments that prevent consent and/or completing experimental tasks
* remote participants need access to a tablet, laptop, or desktop computer to complete tasks.

Exclusion Criteria:

* professional caregivers
* former caregivers who are not currently caring for someone living with dementia
* caregivers providing assistance to someone with normal cognition

Where it's running

  • Texas Christian University
    Fort Worth, Texas, United States
    Recruiting
  • Virginia Wesleyan University
    Norfolk, Virginia, United States
    Not yet recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.