This article describes the study design of a dual-objective, Phase III clinical trial in individuals presymptomatic for Alzheimer’s disease. It addresses the particular challenges for delay and prevention studies. These include:
- Ensuring that the trial population, cognitively normal at outset, contains a sufficient number of participants at increased risk of cognitive impairment onset during the trial time frame to avoid prohibitive trial size and duration.
- Finding appropriate measures to detect the earliest signs of disease and track cognitive decline.
- Building in procedural flexibility to retain participants through the long duration of delay and prevention trials.
Burns DK, Chiang C, Welsh-Bohmer KA, et al. The TOMMORROW study: Design of an Alzheimer's disease delay-of-onset clinical trial . Alzheimer’s & Dementia 2019;5:661–670.
2c7a2ab67c334cdd505d4200a1b65663 Recruit & Retain Participants Manage Research Operations 2019-12-13T00:00:00Z Cognitive Status Trial Design Research Articles
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