Alzheimer’s disease and related dementias (ADRD) affect 47 million people worldwide—a number expected to double every 20 years. Yet, research lacks diversity, especially for underrepresented populations, creating gaps in understanding how different communities experience ADRD and respond to treatments.
The core set of digital measures of ADRD provide you with metrics that connect technology to the real experiences of patients and their care partners based on DATAcc’s survey of the global ADRD community. Use these resources to enhance your trial process, ensure consistent data across studies, support diverse recruitment, and enable real-time insights for earlier, data-driven decisions.
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