This is a randomized, decentralized, non-interventional clinical study. The primary objective of this study is to develop execution and efficiency metrics from completion of this study to inform on the potential design for future projects. The secondary objective of this study is to assess the main study endpoints across balanced attributes of study sub-populations.
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Interaction efficiency (contacted vs. enrolled)
Timeframe: 4 weeks post Last Subject's remote visit
Percent completion of subject self-taken images
Timeframe: 4 weeks post Last Subject's remote visit
Percent completion of subjects participating in bio-sampling subset
Timeframe: 4 weeks post Last Subject's remote visit