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EndeavorOTC™ Prospective Product Registry

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Akili Interactive Labs

Status

Active, not recruiting

Conditions

ADHD

Treatments

Device: EndeavorOTC

Study type

Observational

Funder types

Industry

Identifiers

NCT06109051
Akili-065

Details and patient eligibility

About

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.

Full 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.

Enrollment

198 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Has an active EndeavorOTC™subscription
  • Provide informed consent to participate in the registry

Exclusion criteria

  • N/A

Trial design

198 participants in 1 patient group

EndeavorOTC Users
Description:
All users who subscribe to EndeavorOTC for any duration
Treatment:
Device: EndeavorOTC

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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