[Online] The Neureka Project

  • STATUS
    Recruiting
  • End date
    Dec 31, 2030
Updated on 29 April 2021
Investigator
Dr Claire Gillan
Primary Contact
[Online] The Neureka Project (4.0 mi away) Contact
+240 other location

Summary

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.


Description

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.

Details
Condition Depression, Obsessive-Compulsive Disorder, Dementia, Depression (Major/Severe), Depression (Adolescent), Depression (Pediatric), Depression (Adult and Geriatric), Depression (Treatment-Resistant), Anxiety Disorders, *Healthy Volunteers
Clinical Study IdentifierTX264193
Last Modified on29 April 2021

Eligibility

How to participate?

Step 1 Connect with a site
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.

You are contacting

Investigator Avatar
Name

Primary Contact

site
Name

0/250
Preferred Language
Other Language
Please verify that you are not a bot.

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

Learn more

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.

Learn more

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

Learn more

Similar trials to consider

Loading...

Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer

user name

Added by • 

 • 

Private

Reply by • Private
Loading...

Lorem ipsum dolor sit amet consectetur, adipisicing elit. Ipsa vel nobis alias. Quae eveniet velit voluptate quo doloribus maxime et dicta in sequi, corporis quod. Ea, dolor eius? Dolore, vel!

  The passcode will expire in None.
Loading...

No annotations made yet

Add a private note
  • abc Select a piece of text from the left.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.
Add a private note