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Clinical Trial Summary

The EndeavorOTC product registry aims to collect real world data from EndeavorOTC users. The objectives of this registry are to describe clinical and demographic characteristics, treatment patterns, clinical and quality of life outcomes, and healthcare utilization in EndeavorOTC users in a real-world setting.


Clinical Trial Description

All EndeavorOTC users who subscribe to EndeavorOTC are invited to participate in this product registry. Users must provide their informed consent and have an active subscription to the product at time of enrollment to participate. Study activities are emailed to participants at baseline, 1, 2, 3, 6, 9, and 12-months after enrollment. Study activities consist of an online survey and online ADHD assessment. All data are captured electronically and securely through commercial data capture platforms. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06109051
Study type Observational [Patient Registry]
Source Akili Interactive Labs, Inc.
Contact
Status Enrolling by invitation
Phase
Start date October 3, 2023
Completion date December 31, 2026

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