Alzheimer's & Dementia Outreach, Recruitment & Engagement Resources
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Displaying 1 - 10 of 18 resources.
- This article explores demographic differences in intention of older adults to join an Alzheimer’s registry using national survey data.
- This article identifies barriers and facilitators to Alzheimer’s registry recruitment via mobile device.
- This article summarizes findings from qualitative interviews with Black and White prospective participants that identified barriers and facilitators to Alzheimer’s research recruitment.
- This article describes how caring behaviors by recruiters impact recruitment in African American and Non-Latinx White older adults.
- In this article, researchers examine the effectiveness of a community-based strategy to recruit participants for a dementia study.
- This article examines how race and ethnic background impacts sources of recruitment and eligibility for an Alzheimer’s preclinical trial.
- This research examined the effectiveness and differences in using both traditional and social media materials for the recruitment of African American versus non-Hispanic white participants.
- Researchers looked at how enrollment factors made a difference, broken out by race, on the progression of mild cognitive impairment and dementia. Using Alzheimer’s Disease Research Center data, they examined the rate of impairment between white participants and Black participants with age-at-progression survival models.
- Researchers surveyed 1,643 participants to investigate potential motivators, barriers, and facilitators to participation in research that tests a new drug or device. Participants were Caucasian, African American, Hispanic, multiracial, and "other" minorities. Motivators were measured on a scale that ranged from "no influence" (0) to "most influence" (4). Significant differences by race were found for five out of 10 motivating factors. "Risk of unknown side-effects" was the greatest barrier for...
- A telephone survey of 511 people in one Southern state explored the communication sources and perceived effective communication channels and strategies through which African Americans and White individuals receive clinical trial information.