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Privacy, Trust, and Consent in Aging Research Recruitment

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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