Randomized Controlld Trial of Dementia Education Resources for Action
Part of paid clinical trials in Fairfax, Virginia.
- Sponsor
- George Mason University
- Study ID
- NCT07545577
- Status
- Recruiting
Conditions
- Alzheimer's Disease and Related Dementia
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Accepted
Interventions
- DERA Online Training Program — BEHAVIORALThe Dementia Education and Resources for Action (DERA) program is a structured, online training intervention designed for community health workers. The program consists of approximately 7 sessions delivered through a web-based platform. Content includes dementia fundamentals, early signs and risk factors, stigma reduction, and strategies for communication, support, and service navigation. The training incorporates video-based instruction, interactive materials, and quizzes to support learning and engagement.
Study Details
The goal of this intervention trial is to evaluate the effectiveness the online training program Dementia Education and Resources for Action (DERA) in improving Alzheimer's disease and related dementia-(ADRD) knowledge, stigma, and service-related self-efficacy among community health workers (CHWs). We hypothesize that participants who have completed the DERA will have improved ADRD knowledge and self-efficacy in related service and reduced stigma against ADRD and people affected.
Key Dates
- First listed
- Apr 22, 2026
- Start date
- Jun 16, 2026
- Status verified
- May 2026
- Primary completion
- Dec 30, 2026
- Completion
- Aug 31, 2027
Study Design
- Enrollment
- 100 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- OTHER
Arms
- Experimental: Immediate DERA InterventionParticipants assigned to this arm will receive immediate access to the DERA online training program. The program is web-based platform and includes 7 structured modules on dementia knowledge, stigma reduction, and the role of community health workers in supporting individuals with dementia and their caregivers.
- No Intervention: Waitlist ControlParticipants assigned to this arm will not receive access to the DERA program during the study period. They will complete baseline and post-intervention assessments over a similar timeframe as the intervention group. After completion of the post-intervention assessment, participants will be provided access to the DERA training program.
Primary Outcome Measure
Dementia Knowledge [ Time Frame: Baseline to post-intervention (approximately 6-8 weeks) ]
Central Contacts
- Alicia Hong7039931929
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Online | Fairfax | Virginia | 22030 |
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