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April 30, 2026 | 3:-0AM – 4:30PM ET

A new generation of Alzheimer’s treatments is reshaping the landscape of dementia care. This webinar will examine what these drugs are, how they differ from previous therapies that primarily addressed symptoms, and what we know about their benefits and risks. Have these treatments changed patient care in meaningful ways? How are patients and families experiencing them in the real world? We will also explore pressing questions about affordability and access—particularly given that most people living with dementia rely on Medicare—and consider whether the clinical benefits observed to date justify the costs within a constrained health care system.


At the same time, advances in blood-based biomarkers now allow clinicians to detect Alzheimer’s-related brain changes before symptoms appear, raising complex ethical and clinical questions. How should this information be used, especially when many people with biomarker evidence may never develop dementia? The conversation will also address widespread claims about preventing cognitive decline—from coffee consumption to brain-training apps—separating evidence from hype. Finally, we will look ahead to the research frontier, highlighting the most promising scientific hypotheses and emerging approaches that could shape the next era of Alzheimer’s prevention and treatment.





May 20-21, 2026

This workshop will include sessions on Multidisciplinary Teams, Early Translation, Multidisciplinary Communities/Geroscience, and Tools and Barriers in Multidisciplinary Research. View the current agenda for the workshop here. This workshop will be held in-person and streamed virtually on May 20 and 21, 2026. Registration to attend virtual sessions is free and open to the public. The deadline to register is May 19 at 9am ET.



April 27-28, 2026 | 11:30AM – 4:00PM ET

Purpose and Background

This two-day workshop addresses critical challenges in recruiting participants for aging and Alzheimer's Disease and Related Dementias (AD/ADRD) research while also maintaining robust privacy protections and informed consent processes. As clinical trials increasingly leverage digital technologies, artificial intelligence, and multi-site data partnerships, researchers must navigate complex ethical considerations and regulatory requirements to build and sustain trust with older adult populations.

The workshop brings together leading experts in bioethics, data privacy, health law, technology innovation, and community engagement to explore best practices in privacy-preserving recruitment strategies, accessible consent processes for individuals with varied cognitive abilities, federal data partnerships, and sustainable infrastructure for participant engagement. Sessions will address regulatory compliance, AI-driven recruitment tools, community-based strategies, and cost-effective approaches to broadening trial participation.


Audience

This workshop is designed for professionals engaged in clinical research on aging and Alzheimer’s and related dementias, including the following:

  • Bioethicists and research ethics professionals

  • Institutional Review Board (IRB) members and administrators

  • Clinical trial coordinators and recruitment specialists

  • Data scientists and health informatics professionals

  • Federal and institutional policy makers

  • Patient advocacy organizations

  • Health system administrators and partnership leaders




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