"Without diversity in clinical trials, we're missing pieces of the puzzle that could save lives." This message is central to this episode of Voices of Inclusive Research, where host Renarda Jones chats with Jen Lothridge, a clinical trial participant and advocate, about how inclusive research can transform healthcare for underrepresented communities.
Jen shares her journey in medical research, highlighting the importance of safety, ethics, and informed consent—especially for Black and Brown communities that have been historically mistreated in research. She stresses that trust and cultural competence are crucial to meaningful participation in clinical trials.
This episode is a powerful reminder of the importance of equitable research and the role communities of color can play in shaping a healthier future.
Must-Hear Insights and Key Moments
About Jen Lothridge
Jen (she/her/ella) is a passionate advocate and community leader with over 20 years of experience in social services, specializing in Person-Centered Care. Born and raised in San Diego, she embraces life wholeheartedly and brings a deep commitment to supporting the HIV/AIDS community through volunteer roles with the San Diego County HIV Planning/Community Engagement Group, POZabilities, and other key organizations.
Currently a Bachelor of Social Work and Gerontology student at San Diego State University, Jen also serves as the Aging & Research Program Supervisor at Christie’s Place, where she connects with and empowers individuals facing the challenges of aging.
Her mission extends into healing and trust-building within communities affected by medical injustices, especially among Black and African American women. By promoting informed consent, harm reduction, and trauma-informed care, Jen envisions research participation as a positive path toward advancing medical equity and rebuilding trust in healthcare.
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