Alzheimer's Disease Study Remote Administration Date Published: May 08, 2020 Whitepaper Alzheimer’s Disease studies generally have low success rates so when the COVID-19 pandemic required clinical trials to change to remote administration models, it became more critical than ever to maximize the quantity and quality of data in these studies. Signant Health’s David Miller outlines considerations for optimizing the quality and reliability of remote outcomes assessment data, including: Validating scales for audio and/or video administration Confirming if input is needed from patient and/or caregiver Ensuring all participants understand their roles Considering study drug administration Meeting site location needs Respecting the patient’s discomfort with an at-home administer during COVID-19 Download Now Share: LinkedInTweet Recommended Resources 3 Themes and Takeaways From FDA’s Draft Guidance on DCTs Download Now Whitepaper Computerized Adaptive Tests Using PROMIS CAT Download Now Whitepaper The EMA Recommendation Paper on Decentralized Elements in Clinical Trials: An Overview Read Our White Paper Whitepaper