The Neureka Project

  • End date
    Dec 31, 2030
Updated on 9 March 2023
Online studies
Accepts healthy volunteers


The Neureka Project aims to develop new ways of detecting disorders of the brain early. From mental health conditions to dementia, we want to find out who is at risk and why, so we can develop preventative interventions that can be used the world over. 

To do this, we are taking research out of the lab and into your phone, through the Neureka app. On the app, you can complete science challenges, play games and tells us about your thoughts, feeling, experiences and lifestyle. Every minute you spend on the app helps researchers move the needle forward in the global fight against disorders of the mind. Download the neureka app for free today by searching 'neureka' on the App Store or Google Play Store or use the following link

Check out for more!


Using a smartphone/tablet to complete a series of science challenges and self-report questionnaires. Participation may be ongoing on a rolling daily, weekly, or monthly basis depending on which science challenges the participants engage with.

Condition Depression, Depression (Adult and Geriatric), Depression (Treatment-Resistant), Depression (Major/Severe), Depression, Depression (Pediatric), Depression (Adolescent), Obsessive-Compulsive Disorder, Dementia, Dementia, Depression (Major/Severe), Depression (Adolescent), Depression (Pediatric), Depression (Adult and Geriatric), Depression (Treatment-Resistant), Anxiety Disorders, *Healthy Volunteers, Online, Smartphone, Tablet Device
Clinical Study IdentifierTX291222
Last Modified on9 March 2023


How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer  to help accelerate the development of new treatments and to get notified about similar trials.

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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