Psychosis-Risk Outcomes Study (ProNET)
Research Question:
The goal of the ProNET study is to phenotype 1040 CHR participants and 390 healthy
controls across the ProNET network of 26 international sites with multi-modal biomarkers,
psychopathology and cognition, genetics, body fluid analytes, natural speech/language,
and passive/ecological momentary digital phenotyping, and map these biomarkers onto
a core set of clinical outcome measures and trajectories over 24 months.
Basic Study Information
Purpose:
The purpose of this research study is to collect information from individuals who
are considered at clinically high risk for the possible development of psychosis.
Information will also be collected from healthy individuals who are not considered
at high risk for psychosis. This information will be used to guide future treatments.
Participants will participate in interviews and cognitive tasks, provide blood samples,
saliva and DNA, and get a scan of their brain. You may participate up to 2 years.
You must be between 12 and 30 years old. There are other requirements to join the
study. The study team can review them with you.
Location: URMC, Strong Ties
Study Reference #: STUDY00008405
Lead Researcher (Principal Investigator)
Lead Researcher:
Steven Silverstein
Study Contact Information
Study Coordinator: Iwona Juskiewicz
Phone: (585) 275-4961
Email: iwona_juskiewicz@urmc.rochester.edu
Additional Study Details
Study Details:
Participants enrolled in ProNET will participate in outcome assessments over a two
year period. The assessments include interviews, blood & saliva collection, MRI, EEG,
cognitive testing, digital data collection. The participants will be reimbursed at
the rate of $30/ hour of assessment
Number of Visits:
6 to 10
Parking:
Reimbursed
Transportation Coverage:
Reimbursement:
Yes
Payment Details:
$30/hour of assessment
Learn More About These Conditions
More information about Auditory hallucinations
More information about Hallucinations
More information about Visual hallucinations
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