Скачать или смотреть Caregivers See the Gaps That Research Misses with Stephanie J Monroe, JD

“Don’t come into someone’s home for a party without bringing a gift.” – Stephanie Monroe

In this episode of Voices of Inclusive Research, Dr. Renarda Jones sits down with Stephanie Monroe, advocate and community leader, for an empowering conversation about what true inclusion in clinical research really looks like.

Stephanie shares her perspective on patient-centered care, and why small but vital supports like patient navigators, and trusted advocates make or break participation in clinical trials.

Stephanie illustrates how cultural context and grassroots leadership drive engagement and retention in trials. She also calls out the responsibility of pharmaceutical companies and academic centers to prioritize representation, diversify advisory boards, and honor the wisdom of patients and caregivers in shaping research.

🎧 Tune in for an honest and practical discussion about equity, advocacy, and the power of community to transform health outcomes.

00:00 Introduction and Guest Overview
00:58 Stephanie's Background and Career Journey
01:32 Advocacy and Legislative Work
06:21 Personal Story and Alzheimer's Advocacy
10:51 Challenges in Alzheimer's Research and Diversity
19:19 Addressing Racial Disparities in Alzheimer's Research
19:44 The Importance of Accurate Data Reporting
20:52 Lifestyle Changes for Alzheimer's Prevention
22:06 Advocacy and Community Support
29:27 Final Thoughts and Call to Action

Must-Hear Insights and Key Moments
• Trust Is Earned, Not Assumed – Real partnerships take time, presence, and respect.
• The Details Make the Difference – From parking access to navigation support, small barriers can make or break participation in a clinical trial.
• Representation Creates Belonging – When diverse voices sit on advisory boards, communities see themselves reflected and valued in research decisions.
• Equity Is About People – Clinical research isn’t only about data or science—it’s about families, caregivers, and communities who deserve care and inclusion.

About Stephanie

Stephanie J. Monroe is Vice President and Senior Advisor of Health Equity and Access at UsAgainstAlzheimer’s, where she leads the Center for Brain Health Equity and directs African Americans Against Alzheimer’s—the first national network addressing the disease’s disproportionate impact on African Americans. Through national, local, and strategic partnerships, she raises awareness of disparities, advocates for inclusive clinical trials, and promotes brain health in at-risk communities.

An attorney with three decades in federal policy, Monroe previously served as Assistant Secretary of Education for Civil Rights and spent 25 years on Capitol Hill in senior staff roles, including Chief Counsel of the Senate HELP Committee. She also serves on the National Academy of Sciences Board for Children, Youth, and Families and advises institutions on strategies for inclusive participation in clinical research.

Follow Stephanie J. Monroe
Website: https://www.usagainstalzheimers.org/

Follow Renarda Jones:
Website: https://www.diverseresearchnow.com/
Instagram:   / diverse_research_now  
LinkedIn:   / renardajones  

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